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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362674, constructed from sample accession ERS474273 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_1).  This submission includes reads tagged with the sequence AACGTGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474273">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474273</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581033</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362674</LIBRARY_NAME>
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        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_1#2" accession="ERX1415348" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415348</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362675, constructed from sample accession ERS474282 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_1).  This submission includes reads tagged with the sequence AAACATCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474282">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474282</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581042</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362675</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415349</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362676, constructed from sample accession ERS474302 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_1).  This submission includes reads tagged with the sequence ATGCCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474302">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474302</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581062</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362676</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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      <PRIMARY_ID>ERX1415350</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362677, constructed from sample accession ERS474311 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_1).  This submission includes reads tagged with the sequence AGTGGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474311">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474311</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581071</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362677</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_1#5" accession="ERX1415351" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415351</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362678, constructed from sample accession ERS474326 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_1).  This submission includes reads tagged with the sequence ACCACTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474326">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474326</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581086</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362678</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_1#6" accession="ERX1415352" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415352</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_1#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_1#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362679, constructed from sample accession ERS474337 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_1).  This submission includes reads tagged with the sequence ACATTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474337">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474337</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581097</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362679</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_1#7" accession="ERX1415353" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415353</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362680, constructed from sample accession ERS474345 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_1).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474345">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474345</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581105</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362680</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_1#8" accession="ERX1415354" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415354</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_1#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_1#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362681, constructed from sample accession ERS474358 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_1).  This submission includes reads tagged with the sequence CATCAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474358">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474358</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581118</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362681</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_1#9" accession="ERX1415355" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415355</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_1#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_1#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362682, constructed from sample accession ERS474368 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_1).  This submission includes reads tagged with the sequence CGCTGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474368">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474368</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581128</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362682</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_1#10" accession="ERX1415356" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415356</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_1#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_1#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362683, constructed from sample accession ERS474376 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_1).  This submission includes reads tagged with the sequence ACAAGCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474376">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474376</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581136</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362683</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_1#11" accession="ERX1415357" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415357</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_1#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_1#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362684, constructed from sample accession ERS474391 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_1).  This submission includes reads tagged with the sequence CTGTAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474391">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474391</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581151</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362684</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_1#12" accession="ERX1415358" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415358</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_1#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_1#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362685, constructed from sample accession ERS474404 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_1).  This submission includes reads tagged with the sequence AGTACAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474404">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474404</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581164</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362685</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_2#1" accession="ERX1415359" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415359</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362674, constructed from sample accession ERS474273 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_2).  This submission includes reads tagged with the sequence AACGTGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474273">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474273</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581033</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362674</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_2#2" accession="ERX1415360" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415360</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362675, constructed from sample accession ERS474282 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_2).  This submission includes reads tagged with the sequence AAACATCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474282">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474282</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581042</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362675</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_2#3" accession="ERX1415361" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415361</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362676, constructed from sample accession ERS474302 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_2).  This submission includes reads tagged with the sequence ATGCCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474302">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474302</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581062</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362676</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_2#4" accession="ERX1415362" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415362</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362677, constructed from sample accession ERS474311 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_2).  This submission includes reads tagged with the sequence AGTGGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474311">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474311</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581071</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362677</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_2#5" accession="ERX1415363" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415363</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362678, constructed from sample accession ERS474326 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_2).  This submission includes reads tagged with the sequence ACCACTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474326">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474326</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581086</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362678</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_2#6" accession="ERX1415364" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415364</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362679, constructed from sample accession ERS474337 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_2).  This submission includes reads tagged with the sequence ACATTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474337">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474337</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581097</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362679</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_2#7" accession="ERX1415365" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415365</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_2#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_2#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362680, constructed from sample accession ERS474345 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_2).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474345">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474345</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581105</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362680</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_2#8" accession="ERX1415366" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415366</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_2#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_2#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362681, constructed from sample accession ERS474358 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_2).  This submission includes reads tagged with the sequence CATCAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474358">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474358</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581118</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362681</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_2#9" accession="ERX1415367" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415367</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_2#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_2#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362682, constructed from sample accession ERS474368 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_2).  This submission includes reads tagged with the sequence CGCTGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474368">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474368</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581128</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362682</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_2#10" accession="ERX1415368" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415368</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_2#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_2#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362683, constructed from sample accession ERS474376 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_2).  This submission includes reads tagged with the sequence ACAAGCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474376">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474376</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581136</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362683</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_2#11" accession="ERX1415369" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415369</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_2#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_2#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362684, constructed from sample accession ERS474391 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_2).  This submission includes reads tagged with the sequence CTGTAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474391">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474391</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581151</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362684</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_2#12" accession="ERX1415370" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415370</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_2#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_2#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362685, constructed from sample accession ERS474404 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_2).  This submission includes reads tagged with the sequence AGTACAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474404">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474404</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581164</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362685</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_3#1" accession="ERX1415371" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415371</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_3#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_3#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362686, constructed from sample accession ERS474274 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_3).  This submission includes reads tagged with the sequence AACAACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474274">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474274</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581034</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362686</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_3#2" accession="ERX1415372" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415372</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_3#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_3#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362687, constructed from sample accession ERS474284 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_3).  This submission includes reads tagged with the sequence AACCGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474284">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474284</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581044</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362687</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_3#3" accession="ERX1415373" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415373</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_3#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_3#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362688, constructed from sample accession ERS474303 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_3).  This submission includes reads tagged with the sequence AACGCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474303">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474303</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581063</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362688</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_3#4" accession="ERX1415374" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415374</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_3#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_3#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362689, constructed from sample accession ERS474312 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_3).  This submission includes reads tagged with the sequence AAGACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474312">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474312</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581072</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362689</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_3#5" accession="ERX1415375" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415375</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_3#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_3#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362690, constructed from sample accession ERS474328 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_3).  This submission includes reads tagged with the sequence AAGGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474328">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474328</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581088</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362690</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_3#6" accession="ERX1415376" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415376</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_3#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_3#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362691, constructed from sample accession ERS474338 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_3).  This submission includes reads tagged with the sequence ACACAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474338">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474338</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581098</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362691</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_3#7" accession="ERX1415377" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415377</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_3#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_3#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362692, constructed from sample accession ERS474347 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_3).  This submission includes reads tagged with the sequence ACAGCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474347">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581107</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362692</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_3#8" accession="ERX1415378" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415378</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_3#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_3#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362693, constructed from sample accession ERS474359 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_3).  This submission includes reads tagged with the sequence ACCTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474359">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474359</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581119</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362693</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_3#9" accession="ERX1415379" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415379</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_3#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_3#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362694, constructed from sample accession ERS474369 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_3).  This submission includes reads tagged with the sequence ACGCTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474369">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474369</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581129</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362694</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_3#10" accession="ERX1415380" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415380</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_3#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_3#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362695, constructed from sample accession ERS474377 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_3).  This submission includes reads tagged with the sequence ACGTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474377">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474377</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581137</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362695</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_3#11" accession="ERX1415381" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415381</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_3#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_3#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362696, constructed from sample accession ERS474393 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_3).  This submission includes reads tagged with the sequence ACTATGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474393">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474393</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581153</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362696</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_3#12" accession="ERX1415382" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415382</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_3#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_3#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362697, constructed from sample accession ERS474415 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_3).  This submission includes reads tagged with the sequence AGAGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474415">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474415</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581175</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362697</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_4#1" accession="ERX1415383" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415383</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_4#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_4#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362686, constructed from sample accession ERS474274 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_4).  This submission includes reads tagged with the sequence AACAACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474274">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474274</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581034</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362686</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="439" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_4#2" accession="ERX1415384" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415384</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_4#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_4#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362687, constructed from sample accession ERS474284 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_4).  This submission includes reads tagged with the sequence AACCGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474284">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474284</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581044</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362687</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="439" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_4#3" accession="ERX1415385" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415385</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_4#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_4#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362688, constructed from sample accession ERS474303 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_4).  This submission includes reads tagged with the sequence AACGCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474303">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474303</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581063</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362688</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="439" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_4#4" accession="ERX1415386" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415386</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_4#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_4#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362689, constructed from sample accession ERS474312 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_4).  This submission includes reads tagged with the sequence AAGACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474312">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474312</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581072</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362689</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="439" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_4#5" accession="ERX1415387" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415387</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_4#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_4#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362690, constructed from sample accession ERS474328 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_4).  This submission includes reads tagged with the sequence AAGGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474328">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474328</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581088</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362690</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="439" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_4#6" accession="ERX1415388" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415388</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_4#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_4#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362691, constructed from sample accession ERS474338 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_4).  This submission includes reads tagged with the sequence ACACAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474338">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474338</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581098</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362691</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="439" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_4#7" accession="ERX1415389" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415389</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_4#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_4#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362692, constructed from sample accession ERS474347 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_4).  This submission includes reads tagged with the sequence ACAGCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474347">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581107</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362692</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="439" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_4#8" accession="ERX1415390" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415390</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_4#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_4#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362693, constructed from sample accession ERS474359 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_4).  This submission includes reads tagged with the sequence ACCTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474359">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474359</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581119</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362693</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="439" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_4#10" accession="ERX1415392" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415392</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_4#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_4#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362695, constructed from sample accession ERS474377 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_4).  This submission includes reads tagged with the sequence ACGTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474377">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474377</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581137</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362695</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="439" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_4#11" accession="ERX1415393" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415393</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_4#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_4#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362696, constructed from sample accession ERS474393 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_4).  This submission includes reads tagged with the sequence ACTATGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474393">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474393</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581153</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362696</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="439" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_4#12" accession="ERX1415394" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415394</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_4#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_4#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362697, constructed from sample accession ERS474415 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_4).  This submission includes reads tagged with the sequence AGAGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474415">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474415</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581175</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362697</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="439" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_5#1" accession="ERX1415395" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415395</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_5#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_5#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362698, constructed from sample accession ERS474276 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_5).  This submission includes reads tagged with the sequence AGATCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474276">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474276</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581036</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362698</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_5#2" accession="ERX1415396" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415396</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_5#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_5#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362699, constructed from sample accession ERS474290 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_5).  This submission includes reads tagged with the sequence AGCAGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474290">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474290</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581050</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362699</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_5#3" accession="ERX1415397" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415397</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_5#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_5#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362700, constructed from sample accession ERS474304 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_5).  This submission includes reads tagged with the sequence AGTCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474304">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581064</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362700</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_5#4" accession="ERX1415398" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415398</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_5#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_5#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362701, constructed from sample accession ERS474314 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_5).  This submission includes reads tagged with the sequence ATCCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474314">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474314</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581074</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362701</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_5#5" accession="ERX1415399" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415399</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_5#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_5#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362702, constructed from sample accession ERS474329 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_5).  This submission includes reads tagged with the sequence ATTGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474329">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474329</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581089</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362702</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_5#6" accession="ERX1415400" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415400</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_5#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_5#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362703, constructed from sample accession ERS474339 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_5).  This submission includes reads tagged with the sequence CAACCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474339">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474339</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581099</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362703</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_5#7" accession="ERX1415401" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415401</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_5#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_5#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362704, constructed from sample accession ERS474348 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_5).  This submission includes reads tagged with the sequence GACTAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474348">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581108</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362704</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_5#8" accession="ERX1415402" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415402</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_5#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_5#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362705, constructed from sample accession ERS474361 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_5).  This submission includes reads tagged with the sequence CAATGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474361">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474361</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581121</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362705</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_5#9" accession="ERX1415403" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415403</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_5#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_5#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362706, constructed from sample accession ERS474370 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_5).  This submission includes reads tagged with the sequence CACTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474370">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474370</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581130</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362706</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_5#10" accession="ERX1415404" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415404</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_5#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_5#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362707, constructed from sample accession ERS474378 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_5).  This submission includes reads tagged with the sequence CAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474378">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474378</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581138</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362707</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_5#11" accession="ERX1415405" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415405</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_5#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_5#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362708, constructed from sample accession ERS474395 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_5).  This submission includes reads tagged with the sequence CATACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474395">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474395</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581155</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362708</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_5#12" accession="ERX1415406" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415406</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_5#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_5#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362709, constructed from sample accession ERS474416 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_5).  This submission includes reads tagged with the sequence CCAGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474416">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474416</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581176</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362709</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_6#1" accession="ERX1415407" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415407</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_6#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_6#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362698, constructed from sample accession ERS474276 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_6).  This submission includes reads tagged with the sequence AGATCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474276">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474276</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581036</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362698</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_6#2" accession="ERX1415408" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415408</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_6#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_6#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362699, constructed from sample accession ERS474290 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_6).  This submission includes reads tagged with the sequence AGCAGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474290">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474290</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581050</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362699</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_6#3" accession="ERX1415409" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415409</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_6#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_6#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362700, constructed from sample accession ERS474304 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_6).  This submission includes reads tagged with the sequence AGTCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474304">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581064</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362700</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_6#4" accession="ERX1415410" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415410</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_6#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_6#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362701, constructed from sample accession ERS474314 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_6).  This submission includes reads tagged with the sequence ATCCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474314">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474314</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581074</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362701</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_6#5" accession="ERX1415411" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415411</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_6#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_6#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362702, constructed from sample accession ERS474329 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_6).  This submission includes reads tagged with the sequence ATTGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474329">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474329</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581089</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362702</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_6#6" accession="ERX1415412" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415412</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_6#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_6#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362703, constructed from sample accession ERS474339 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_6).  This submission includes reads tagged with the sequence CAACCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474339">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474339</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581099</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362703</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_6#7" accession="ERX1415413" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415413</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_6#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_6#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362704, constructed from sample accession ERS474348 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_6).  This submission includes reads tagged with the sequence GACTAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474348">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581108</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362704</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_6#8" accession="ERX1415414" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415414</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_6#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_6#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362705, constructed from sample accession ERS474361 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_6).  This submission includes reads tagged with the sequence CAATGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474361">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474361</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581121</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362705</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_6#9" accession="ERX1415415" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415415</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_6#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_6#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362706, constructed from sample accession ERS474370 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_6).  This submission includes reads tagged with the sequence CACTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474370">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474370</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581130</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362706</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_6#10" accession="ERX1415416" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415416</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_6#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_6#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362707, constructed from sample accession ERS474378 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_6).  This submission includes reads tagged with the sequence CAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474378">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474378</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581138</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362707</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_6#11" accession="ERX1415417" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415417</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_6#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_6#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362708, constructed from sample accession ERS474395 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_6).  This submission includes reads tagged with the sequence CATACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474395">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474395</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581155</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362708</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_6#12" accession="ERX1415418" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415418</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_6#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_6#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362709, constructed from sample accession ERS474416 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_6).  This submission includes reads tagged with the sequence CCAGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474416">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474416</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581176</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362709</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_7#1" accession="ERX1415419" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415419</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_7#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_7#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362710, constructed from sample accession ERS474277 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_7).  This submission includes reads tagged with the sequence CCGAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474277">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474277</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581037</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362710</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_7#2" accession="ERX1415420" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415420</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_7#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_7#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362711, constructed from sample accession ERS474292 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_7).  This submission includes reads tagged with the sequence CCGTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474292">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474292</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581052</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362711</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_7#3" accession="ERX1415421" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415421</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_7#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_7#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362712, constructed from sample accession ERS474305 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_7).  This submission includes reads tagged with the sequence CCTCCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474305">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474305</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581065</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362712</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_7#4" accession="ERX1415422" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415422</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_7#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_7#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362713, constructed from sample accession ERS474316 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_7).  This submission includes reads tagged with the sequence CGAACTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474316">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474316</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581076</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362713</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_7#5" accession="ERX1415423" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415423</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_7#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_7#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362714, constructed from sample accession ERS474332 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_7).  This submission includes reads tagged with the sequence CGACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474332">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474332</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581092</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362714</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_7#6" accession="ERX1415424" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415424</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_7#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_7#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362715, constructed from sample accession ERS474340 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_7).  This submission includes reads tagged with the sequence CGCATAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474340">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474340</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581100</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362715</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_7#7" accession="ERX1415425" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415425</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_7#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_7#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362716, constructed from sample accession ERS474349 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_7).  This submission includes reads tagged with the sequence CTCAATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474349">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474349</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581109</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362716</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_7#8" accession="ERX1415426" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415426</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_7#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_7#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362717, constructed from sample accession ERS474362 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_7).  This submission includes reads tagged with the sequence CTGAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474362">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474362</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581122</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362717</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_7#9" accession="ERX1415427" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415427</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_7#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_7#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362718, constructed from sample accession ERS474371 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_7).  This submission includes reads tagged with the sequence CTGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474371">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474371</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581131</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362718</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_7#10" accession="ERX1415428" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415428</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_7#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_7#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362719, constructed from sample accession ERS474385 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_7).  This submission includes reads tagged with the sequence GAATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474385">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474385</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581145</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362719</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_7#11" accession="ERX1415429" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415429</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_7#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_7#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362720, constructed from sample accession ERS474396 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_7).  This submission includes reads tagged with the sequence CAAGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474396">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474396</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581156</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362720</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_7#12" accession="ERX1415430" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415430</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_7#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_7#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362721, constructed from sample accession ERS474418 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_7).  This submission includes reads tagged with the sequence GAGCTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474418">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474418</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581178</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362721</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_8#1" accession="ERX1415431" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415431</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_8#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_8#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362710, constructed from sample accession ERS474277 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_8).  This submission includes reads tagged with the sequence CCGAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474277">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474277</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581037</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362710</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_8#2" accession="ERX1415432" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415432</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_8#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_8#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362711, constructed from sample accession ERS474292 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_8).  This submission includes reads tagged with the sequence CCGTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474292">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474292</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581052</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362711</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_8#3" accession="ERX1415433" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415433</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_8#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_8#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362712, constructed from sample accession ERS474305 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_8).  This submission includes reads tagged with the sequence CCTCCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474305">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474305</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581065</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362712</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_8#4" accession="ERX1415434" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415434</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_8#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_8#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362713, constructed from sample accession ERS474316 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_8).  This submission includes reads tagged with the sequence CGAACTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474316">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474316</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581076</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362713</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_8#5" accession="ERX1415435" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415435</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_8#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_8#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362714, constructed from sample accession ERS474332 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_8).  This submission includes reads tagged with the sequence CGACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474332">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474332</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581092</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362714</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_8#6" accession="ERX1415436" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415436</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_8#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_8#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362715, constructed from sample accession ERS474340 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_8).  This submission includes reads tagged with the sequence CGCATAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474340">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474340</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581100</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362715</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_8#7" accession="ERX1415437" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415437</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_8#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_8#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362716, constructed from sample accession ERS474349 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_8).  This submission includes reads tagged with the sequence CTCAATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474349">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474349</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581109</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362716</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_8#8" accession="ERX1415438" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415438</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_8#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_8#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362717, constructed from sample accession ERS474362 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_8).  This submission includes reads tagged with the sequence CTGAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474362">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474362</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581122</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362717</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_8#9" accession="ERX1415439" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415439</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_8#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_8#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362718, constructed from sample accession ERS474371 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_8).  This submission includes reads tagged with the sequence CTGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474371">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474371</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581131</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362718</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_8#10" accession="ERX1415440" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415440</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_8#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_8#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362719, constructed from sample accession ERS474385 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_8).  This submission includes reads tagged with the sequence GAATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474385">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474385</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581145</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362719</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_8#11" accession="ERX1415441" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415441</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_8#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_8#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362720, constructed from sample accession ERS474396 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_8).  This submission includes reads tagged with the sequence CAAGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474396">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474396</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581156</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362720</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_8#12" accession="ERX1415442" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415442</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_8#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_8#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362721, constructed from sample accession ERS474418 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_8).  This submission includes reads tagged with the sequence GAGCTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474418">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474418</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581178</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362721</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_1#1" accession="ERX1415443" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415443</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362722, constructed from sample accession ERS474278 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_1).  This submission includes reads tagged with the sequence GATAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474278">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474278</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581038</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362722</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_1#2" accession="ERX1415444" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415444</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362723, constructed from sample accession ERS474293 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_1).  This submission includes reads tagged with the sequence GCCACAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474293">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474293</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581053</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362723</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_1#3" accession="ERX1415445" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415445</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362724, constructed from sample accession ERS474307 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_1).  This submission includes reads tagged with the sequence GCGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474307">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474307</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581067</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362724</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_1#4" accession="ERX1415446" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415446</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362725, constructed from sample accession ERS474320 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_1).  This submission includes reads tagged with the sequence GCTAACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474320">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474320</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581080</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362725</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_1#5" accession="ERX1415447" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415447</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362726, constructed from sample accession ERS474333 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_1).  This submission includes reads tagged with the sequence GCTCGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474333">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474333</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581093</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362726</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_1#6" accession="ERX1415448" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415448</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_1#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_1#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362727, constructed from sample accession ERS474341 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_1).  This submission includes reads tagged with the sequence GGAGAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474341">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474341</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581101</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362727</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_1#7" accession="ERX1415449" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415449</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362728, constructed from sample accession ERS474351 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_1).  This submission includes reads tagged with the sequence GGTGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474351">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581111</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362728</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_1#8" accession="ERX1415450" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415450</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_1#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_1#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362729, constructed from sample accession ERS474363 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_1).  This submission includes reads tagged with the sequence GTACGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474363">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474363</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581123</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362729</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_1#9" accession="ERX1415451" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415451</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_1#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_1#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362730, constructed from sample accession ERS474372 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_1).  This submission includes reads tagged with the sequence GTCGTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474372">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474372</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581132</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362730</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_1#10" accession="ERX1415452" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415452</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_1#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_1#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362731, constructed from sample accession ERS474386 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_1).  This submission includes reads tagged with the sequence GTCTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474386">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474386</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581146</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362731</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_1#11" accession="ERX1415453" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415453</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_1#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_1#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362732, constructed from sample accession ERS474397 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_1).  This submission includes reads tagged with the sequence GTGTTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474397">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474397</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581157</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362732</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_1#12" accession="ERX1415454" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415454</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_1#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_1#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362733, constructed from sample accession ERS474419 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_1).  This submission includes reads tagged with the sequence TAGGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474419">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474419</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581179</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362733</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_2#1" accession="ERX1415455" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415455</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362722, constructed from sample accession ERS474278 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_2).  This submission includes reads tagged with the sequence GATAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474278">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474278</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581038</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362722</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_2#2" accession="ERX1415456" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415456</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362723, constructed from sample accession ERS474293 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_2).  This submission includes reads tagged with the sequence GCCACAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474293">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474293</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581053</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362723</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_2#3" accession="ERX1415457" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415457</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362724, constructed from sample accession ERS474307 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_2).  This submission includes reads tagged with the sequence GCGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474307">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474307</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581067</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362724</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_2#4" accession="ERX1415458" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415458</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362725, constructed from sample accession ERS474320 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_2).  This submission includes reads tagged with the sequence GCTAACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474320">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474320</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581080</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362725</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_2#5" accession="ERX1415459" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415459</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362726, constructed from sample accession ERS474333 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_2).  This submission includes reads tagged with the sequence GCTCGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474333">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474333</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581093</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362726</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_2#6" accession="ERX1415460" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415460</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362727, constructed from sample accession ERS474341 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_2).  This submission includes reads tagged with the sequence GGAGAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474341">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474341</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581101</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362727</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_2#7" accession="ERX1415461" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415461</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_2#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_2#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362728, constructed from sample accession ERS474351 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_2).  This submission includes reads tagged with the sequence GGTGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474351">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581111</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362728</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_2#8" accession="ERX1415462" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415462</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_2#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_2#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362729, constructed from sample accession ERS474363 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_2).  This submission includes reads tagged with the sequence GTACGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474363">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474363</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581123</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362729</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_2#9" accession="ERX1415463" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415463</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_2#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_2#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362730, constructed from sample accession ERS474372 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_2).  This submission includes reads tagged with the sequence GTCGTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474372">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474372</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581132</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362730</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_2#10" accession="ERX1415464" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415464</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_2#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_2#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362731, constructed from sample accession ERS474386 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_2).  This submission includes reads tagged with the sequence GTCTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474386">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474386</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581146</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362731</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_2#11" accession="ERX1415465" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415465</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_2#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_2#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362732, constructed from sample accession ERS474397 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_2).  This submission includes reads tagged with the sequence GTGTTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474397">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474397</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581157</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362732</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_3#1" accession="ERX1415467" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415467</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_3#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_3#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362734, constructed from sample accession ERS474279 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_3).  This submission includes reads tagged with the sequence TATCAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474279">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474279</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581039</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362734</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_3#2" accession="ERX1415468" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415468</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_3#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_3#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362735, constructed from sample accession ERS474294 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_3).  This submission includes reads tagged with the sequence TCCGTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474294">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474294</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581054</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362735</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_3#4" accession="ERX1415470" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415470</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_3#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_3#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362737, constructed from sample accession ERS474322 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_3).  This submission includes reads tagged with the sequence TGAAGAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474322">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474322</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581082</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362737</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_3#5" accession="ERX1415471" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415471</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_3#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_3#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362738, constructed from sample accession ERS474334 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_3).  This submission includes reads tagged with the sequence TGGAACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474334">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474334</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581094</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362738</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_3#7" accession="ERX1415473" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415473</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_3#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_3#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362740, constructed from sample accession ERS474352 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_3).  This submission includes reads tagged with the sequence TGGTGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474352">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581112</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362740</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_3#8" accession="ERX1415474" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415474</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_3#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_3#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362741, constructed from sample accession ERS474364 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_3).  This submission includes reads tagged with the sequence TTCACGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474364">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474364</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581124</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362741</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_3#10" accession="ERX1415476" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415476</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_3#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_3#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362743, constructed from sample accession ERS474387 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_3).  This submission includes reads tagged with the sequence AAGAGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474387">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474387</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581147</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362743</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_3#11" accession="ERX1415477" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415477</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_3#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_3#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362744, constructed from sample accession ERS474398 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_3).  This submission includes reads tagged with the sequence AAGGACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474398">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474398</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581158</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362744</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_4#1" accession="ERX1415479" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415479</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_4#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_4#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362734, constructed from sample accession ERS474279 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_4).  This submission includes reads tagged with the sequence TATCAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474279">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474279</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581039</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362734</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_4#2" accession="ERX1415480" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415480</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_4#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_4#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362735, constructed from sample accession ERS474294 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_4).  This submission includes reads tagged with the sequence TCCGTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474294">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474294</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581054</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362735</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_4#4" accession="ERX1415482" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415482</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_4#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_4#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362737, constructed from sample accession ERS474322 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_4).  This submission includes reads tagged with the sequence TGAAGAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474322">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474322</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581082</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362737</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_4#5" accession="ERX1415483" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415483</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_4#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_4#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362738, constructed from sample accession ERS474334 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_4).  This submission includes reads tagged with the sequence TGGAACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474334">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474334</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581094</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362738</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_4#7" accession="ERX1415485" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415485</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_4#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_4#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362740, constructed from sample accession ERS474352 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_4).  This submission includes reads tagged with the sequence TGGTGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474352">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581112</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362740</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_4#8" accession="ERX1415486" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415486</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_4#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_4#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362741, constructed from sample accession ERS474364 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_4).  This submission includes reads tagged with the sequence TTCACGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474364">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474364</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581124</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362741</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_4#10" accession="ERX1415488" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415488</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_4#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_4#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362743, constructed from sample accession ERS474387 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_4).  This submission includes reads tagged with the sequence AAGAGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474387">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474387</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581147</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362743</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_4#11" accession="ERX1415489" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415489</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_4#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_4#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362744, constructed from sample accession ERS474398 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_4).  This submission includes reads tagged with the sequence AAGGACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474398">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474398</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581158</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362744</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_5#1" accession="ERX1415491" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415491</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_5#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_5#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362746, constructed from sample accession ERS474280 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_5).  This submission includes reads tagged with the sequence AATGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474280">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474280</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581040</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362746</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_5#2" accession="ERX1415492" broker_name="">
    <IDENTIFIERS>
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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_5#2</SUBMITTER_ID>
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    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
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        <PRIMARY_ID>ERP006001</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362747, constructed from sample accession ERS474295 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_5).  This submission includes reads tagged with the sequence ACACGAC.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>ERS474295</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581055</EXTERNAL_ID>
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          <PAIRED NOMINAL_LENGTH="443" NOMINAL_SDEV="89"/>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <PRIMARY_ID>ERX1415494</PRIMARY_ID>
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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_5#4</SUBMITTER_ID>
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    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
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      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362749, constructed from sample accession ERS474324 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_5).  This submission includes reads tagged with the sequence AGATGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474324">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474324</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581084</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362749</LIBRARY_NAME>
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        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="443" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <SUBMITTER_ID namespace="SC">SC_EXP_18648_5#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_5#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362750, constructed from sample accession ERS474335 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_5).  This submission includes reads tagged with the sequence AGCACCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474335">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474335</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581095</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362750</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_5#7" accession="ERX1415497" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415497</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_5#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_5#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362752, constructed from sample accession ERS474353 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_5).  This submission includes reads tagged with the sequence AGGCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474353">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474353</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581113</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362752</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_5#8" accession="ERX1415498" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415498</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_5#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_5#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362753, constructed from sample accession ERS474366 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_5).  This submission includes reads tagged with the sequence ATAGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474366">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474366</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581126</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362753</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_5#10" accession="ERX1415500" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415500</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_5#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_5#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362755, constructed from sample accession ERS474389 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_5).  This submission includes reads tagged with the sequence ATTGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474389">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474389</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581149</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362755</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_5#11" accession="ERX1415501" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415501</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_5#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_5#11</SUBMITTER_ID>
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    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362756, constructed from sample accession ERS474400 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_5).  This submission includes reads tagged with the sequence CAAGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474400">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474400</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581160</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362756</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_6#1" accession="ERX1415503" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415503</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_6#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_6#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362746, constructed from sample accession ERS474280 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_6).  This submission includes reads tagged with the sequence AATGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474280">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474280</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581040</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362746</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_6#2" accession="ERX1415504" broker_name="">
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      <PRIMARY_ID>ERX1415504</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_6#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_6#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362747, constructed from sample accession ERS474295 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_6).  This submission includes reads tagged with the sequence ACACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474295">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474295</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581055</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362747</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_6#4" accession="ERX1415506" broker_name="">
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      <PRIMARY_ID>ERX1415506</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_6#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_6#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362749, constructed from sample accession ERS474324 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_6).  This submission includes reads tagged with the sequence AGATGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474324">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474324</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581084</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362749</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_6#5" accession="ERX1415507" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415507</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_6#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_6#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362750, constructed from sample accession ERS474335 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_6).  This submission includes reads tagged with the sequence AGCACCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474335">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474335</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581095</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362750</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_6#7" accession="ERX1415509" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415509</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_6#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_6#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362752, constructed from sample accession ERS474353 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_6).  This submission includes reads tagged with the sequence AGGCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474353">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474353</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581113</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362752</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_6#8" accession="ERX1415510" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415510</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_6#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_6#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362753, constructed from sample accession ERS474366 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_6).  This submission includes reads tagged with the sequence ATAGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474366">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474366</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581126</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362753</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_6#10" accession="ERX1415512" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415512</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_6#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_6#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362755, constructed from sample accession ERS474389 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_6).  This submission includes reads tagged with the sequence ATTGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474389">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474389</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581149</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362755</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_6#11" accession="ERX1415513" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415513</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_6#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_6#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362756, constructed from sample accession ERS474400 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_6).  This submission includes reads tagged with the sequence CAAGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474400">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474400</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581160</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362756</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_7#1" accession="ERX1415515" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415515</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_7#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_7#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362758, constructed from sample accession ERS474281 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_7).  This submission includes reads tagged with the sequence CCATCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474281">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474281</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581041</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362758</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_7#2" accession="ERX1415516" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415516</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_7#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_7#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362759, constructed from sample accession ERS474301 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_7).  This submission includes reads tagged with the sequence CCGACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474301">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474301</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581061</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362759</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_7#4" accession="ERX1415518" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415518</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_7#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_7#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362761, constructed from sample accession ERS474325 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_7).  This submission includes reads tagged with the sequence CCTCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474325">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474325</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581085</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362761</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_7#5" accession="ERX1415519" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415519</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_7#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_7#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362762, constructed from sample accession ERS474336 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_7).  This submission includes reads tagged with the sequence CGACACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474336">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474336</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581096</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362762</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_7#7" accession="ERX1415521" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415521</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_7#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_7#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362764, constructed from sample accession ERS474355 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_7).  This submission includes reads tagged with the sequence CTAAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474355">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474355</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581115</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362764</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_7#8" accession="ERX1415522" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415522</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_7#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_7#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362765, constructed from sample accession ERS474367 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_7).  This submission includes reads tagged with the sequence GAACAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474367">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474367</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581127</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362765</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_7#10" accession="ERX1415524" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415524</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_7#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_7#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362767, constructed from sample accession ERS474390 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_7).  This submission includes reads tagged with the sequence GAGTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474390">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474390</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581150</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362767</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_7#11" accession="ERX1415525" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415525</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_7#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_7#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362768, constructed from sample accession ERS474403 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_7).  This submission includes reads tagged with the sequence GATGAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474403">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474403</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581163</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362768</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_8#1" accession="ERX1415527" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415527</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_8#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_8#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362758, constructed from sample accession ERS474281 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_8).  This submission includes reads tagged with the sequence CCATCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474281">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474281</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581041</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362758</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_8#2" accession="ERX1415528" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415528</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_8#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_8#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362759, constructed from sample accession ERS474301 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_8).  This submission includes reads tagged with the sequence CCGACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474301">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474301</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581061</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362759</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_8#4" accession="ERX1415530" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415530</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_8#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_8#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362761, constructed from sample accession ERS474325 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_8).  This submission includes reads tagged with the sequence CCTCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474325">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474325</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581085</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362761</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_8#5" accession="ERX1415531" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415531</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_8#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_8#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362762, constructed from sample accession ERS474336 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_8).  This submission includes reads tagged with the sequence CGACACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474336">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474336</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581096</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362762</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_8#7" accession="ERX1415533" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415533</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_8#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_8#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362764, constructed from sample accession ERS474355 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_8).  This submission includes reads tagged with the sequence CTAAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474355">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474355</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581115</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362764</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18647_4#9" accession="ERX1415391" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415391</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18647_4#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18647_4#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362694, constructed from sample accession ERS474369 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18647_4).  This submission includes reads tagged with the sequence ACGCTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474369">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474369</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581129</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362694</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="439" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_2#12" accession="ERX1415466" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415466</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_2#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_2#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362733, constructed from sample accession ERS474419 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_2).  This submission includes reads tagged with the sequence TAGGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474419">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474419</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581179</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362733</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_3#3" accession="ERX1415469" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415469</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_3#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_3#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362736, constructed from sample accession ERS474308 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_3).  This submission includes reads tagged with the sequence TCTTCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474308">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474308</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581068</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362736</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_3#6" accession="ERX1415472" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415472</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_3#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_3#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362739, constructed from sample accession ERS474342 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_3).  This submission includes reads tagged with the sequence TGGCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474342">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474342</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581102</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362739</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_3#9" accession="ERX1415475" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415475</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_3#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_3#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362742, constructed from sample accession ERS474373 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_3).  This submission includes reads tagged with the sequence AACTCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474373">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474373</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581133</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362742</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_3#12" accession="ERX1415478" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415478</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_3#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_3#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362745, constructed from sample accession ERS474420 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_3).  This submission includes reads tagged with the sequence AATCCGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474420">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474420</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581180</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362745</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_4#3" accession="ERX1415481" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415481</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_4#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_4#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362736, constructed from sample accession ERS474308 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_4).  This submission includes reads tagged with the sequence TCTTCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474308">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474308</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581068</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362736</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_4#6" accession="ERX1415484" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415484</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_4#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_4#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362739, constructed from sample accession ERS474342 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_4).  This submission includes reads tagged with the sequence TGGCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474342">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474342</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581102</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362739</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_4#9" accession="ERX1415487" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415487</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_4#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_4#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362742, constructed from sample accession ERS474373 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_4).  This submission includes reads tagged with the sequence AACTCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474373">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474373</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581133</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362742</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_4#12" accession="ERX1415490" broker_name="">
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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_4#12</SUBMITTER_ID>
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    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
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        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
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      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362745, constructed from sample accession ERS474420 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_4).  This submission includes reads tagged with the sequence AATCCGTC.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>ERS474420</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581180</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362745</LIBRARY_NAME>
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        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="434" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_5#3" accession="ERX1415493" broker_name="">
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      <PRIMARY_ID>ERX1415493</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_5#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_5#3</SUBMITTER_ID>
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    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362748, constructed from sample accession ERS474309 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_5).  This submission includes reads tagged with the sequence ACAGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474309">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474309</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581069</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362748</LIBRARY_NAME>
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        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="443" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_5#6" accession="ERX1415496" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415496</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_5#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_5#6</SUBMITTER_ID>
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    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362751, constructed from sample accession ERS474343 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_5).  This submission includes reads tagged with the sequence AGCCATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474343">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474343</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581103</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362751</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_5#9" accession="ERX1415499" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415499</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_5#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_5#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362754, constructed from sample accession ERS474374 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_5).  This submission includes reads tagged with the sequence ATCATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474374">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474374</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581134</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362754</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_5#12" accession="ERX1415502" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415502</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_5#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_5#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362757, constructed from sample accession ERS474421 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_5).  This submission includes reads tagged with the sequence CACCTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474421">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474421</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581181</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362757</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_6#3" accession="ERX1415505" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415505</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_6#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_6#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362748, constructed from sample accession ERS474309 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_6).  This submission includes reads tagged with the sequence ACAGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474309">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474309</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581069</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362748</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_6#6" accession="ERX1415508" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415508</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_6#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_6#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362751, constructed from sample accession ERS474343 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_6).  This submission includes reads tagged with the sequence AGCCATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474343">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474343</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581103</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362751</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_6#9" accession="ERX1415511" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415511</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_6#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_6#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362754, constructed from sample accession ERS474374 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_6).  This submission includes reads tagged with the sequence ATCATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474374">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474374</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581134</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362754</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_6#12" accession="ERX1415514" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415514</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_6#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_6#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362757, constructed from sample accession ERS474421 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_6).  This submission includes reads tagged with the sequence CACCTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474421">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474421</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581181</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362757</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_7#3" accession="ERX1415517" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415517</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_7#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_7#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362760, constructed from sample accession ERS474310 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_7).  This submission includes reads tagged with the sequence CCTAATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474310">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474310</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581070</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362760</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_7#6" accession="ERX1415520" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415520</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_7#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_7#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362763, constructed from sample accession ERS474344 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_7).  This submission includes reads tagged with the sequence CGGATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474344">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474344</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581104</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362763</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_7#9" accession="ERX1415523" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415523</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_7#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_7#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362766, constructed from sample accession ERS474375 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_7).  This submission includes reads tagged with the sequence GACAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474375">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474375</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581135</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362766</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_7#12" accession="ERX1415526" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415526</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_7#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_7#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362769, constructed from sample accession ERS474422 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_7).  This submission includes reads tagged with the sequence GCCAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474422">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474422</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581182</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362769</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_8#3" accession="ERX1415529" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415529</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_8#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_8#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362760, constructed from sample accession ERS474310 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_8).  This submission includes reads tagged with the sequence CCTAATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474310">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474310</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581070</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362760</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_8#6" accession="ERX1415532" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415532</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_8#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_8#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362763, constructed from sample accession ERS474344 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_8).  This submission includes reads tagged with the sequence CGGATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474344">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474344</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581104</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362763</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_8#8" accession="ERX1415534" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415534</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_8#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_8#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362765, constructed from sample accession ERS474367 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_8).  This submission includes reads tagged with the sequence GAACAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474367">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474367</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581127</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362765</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_8#9" accession="ERX1415535" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415535</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_8#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_8#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362766, constructed from sample accession ERS474375 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_8).  This submission includes reads tagged with the sequence GACAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474375">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474375</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581135</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362766</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_8#10" accession="ERX1415536" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415536</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_8#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_8#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362767, constructed from sample accession ERS474390 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_8).  This submission includes reads tagged with the sequence GAGTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474390">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474390</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581150</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362767</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_8#11" accession="ERX1415537" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415537</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_8#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_8#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362768, constructed from sample accession ERS474403 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_8).  This submission includes reads tagged with the sequence GATGAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474403">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474403</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581163</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362768</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18648_8#12" accession="ERX1415538" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415538</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18648_8#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18648_8#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362769, constructed from sample accession ERS474422 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18648_8).  This submission includes reads tagged with the sequence GCCAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474422">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474422</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581182</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362769</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_1#1" accession="ERX1415539" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415539</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458881, constructed from sample accession ERS474423 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_1).  This submission includes reads tagged with the sequence AACGTGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474423">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474423</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581183</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458881</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_1#2" accession="ERX1415540" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415540</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458882, constructed from sample accession ERS474432 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_1).  This submission includes reads tagged with the sequence AAACATCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474432">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474432</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581192</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458882</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_1#3" accession="ERX1415541" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415541</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458883, constructed from sample accession ERS474444 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_1).  This submission includes reads tagged with the sequence ATGCCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474444">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474444</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581204</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458883</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_1#4" accession="ERX1415542" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415542</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458884, constructed from sample accession ERS474453 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_1).  This submission includes reads tagged with the sequence AGTGGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474453">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474453</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581213</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458884</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_1#5" accession="ERX1415543" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415543</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458885, constructed from sample accession ERS474464 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_1).  This submission includes reads tagged with the sequence ACCACTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474464">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474464</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581224</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458885</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_1#6" accession="ERX1415544" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415544</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_1#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_1#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458886, constructed from sample accession ERS474472 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_1).  This submission includes reads tagged with the sequence ACATTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474472">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474472</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581232</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458886</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_1#7" accession="ERX1415545" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415545</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458887, constructed from sample accession ERS474481 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_1).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474481">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474481</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581241</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458887</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_1#8" accession="ERX1415546" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415546</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_1#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_1#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458888, constructed from sample accession ERS474494 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_1).  This submission includes reads tagged with the sequence CATCAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474494">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474494</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581254</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458888</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_1#9" accession="ERX1415547" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415547</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_1#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_1#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458889, constructed from sample accession ERS474503 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_1).  This submission includes reads tagged with the sequence CGCTGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474503">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474503</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581263</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458889</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_1#10" accession="ERX1415548" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415548</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_1#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_1#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458890, constructed from sample accession ERS474515 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_1).  This submission includes reads tagged with the sequence ACAAGCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474515">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474515</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581275</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458890</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_1#11" accession="ERX1415549" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415549</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_1#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_1#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458891, constructed from sample accession ERS474525 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_1).  This submission includes reads tagged with the sequence CTGTAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474525">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474525</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581285</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458891</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_1#12" accession="ERX1415550" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415550</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_1#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_1#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458892, constructed from sample accession ERS474533 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_1).  This submission includes reads tagged with the sequence AGTACAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474533">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474533</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581293</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458892</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_2#1" accession="ERX1415551" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415551</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458893, constructed from sample accession ERS474424 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_2).  This submission includes reads tagged with the sequence AACAACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474424">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474424</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581184</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458893</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_2#2" accession="ERX1415552" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415552</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458894, constructed from sample accession ERS474433 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_2).  This submission includes reads tagged with the sequence AACCGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474433">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474433</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581193</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458894</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_2#3" accession="ERX1415553" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415553</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458895, constructed from sample accession ERS474446 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_2).  This submission includes reads tagged with the sequence AACGCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474446">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474446</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581206</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458895</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_2#4" accession="ERX1415554" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415554</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458896, constructed from sample accession ERS474454 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_2).  This submission includes reads tagged with the sequence AAGACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474454">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474454</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581214</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458896</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_2#5" accession="ERX1415555" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415555</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458897, constructed from sample accession ERS474465 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_2).  This submission includes reads tagged with the sequence AAGGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474465">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474465</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581225</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458897</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_2#6" accession="ERX1415556" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415556</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458898, constructed from sample accession ERS474473 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_2).  This submission includes reads tagged with the sequence ACACAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474473">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474473</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581233</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458898</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_2#7" accession="ERX1415557" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415557</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_2#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_2#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458899, constructed from sample accession ERS474483 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_2).  This submission includes reads tagged with the sequence ACAGCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474483">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474483</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581243</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458899</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_2#8" accession="ERX1415558" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415558</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_2#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_2#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458900, constructed from sample accession ERS474495 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_2).  This submission includes reads tagged with the sequence ACCTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474495">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474495</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581255</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458900</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_2#9" accession="ERX1415559" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415559</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_2#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_2#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458901, constructed from sample accession ERS474505 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_2).  This submission includes reads tagged with the sequence ACGCTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474505">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474505</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581265</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458901</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_2#10" accession="ERX1415560" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415560</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_2#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_2#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458902, constructed from sample accession ERS474517 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_2).  This submission includes reads tagged with the sequence ACGTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474517">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474517</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581277</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458902</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_2#11" accession="ERX1415561" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415561</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_2#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_2#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458903, constructed from sample accession ERS474526 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_2).  This submission includes reads tagged with the sequence ACTATGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474526">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474526</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581286</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458903</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_2#12" accession="ERX1415562" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415562</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_2#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_2#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458904, constructed from sample accession ERS474537 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_2).  This submission includes reads tagged with the sequence AGAGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474537">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474537</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581297</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458904</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_3#1" accession="ERX1415563" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415563</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_3#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_3#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458905, constructed from sample accession ERS474425 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_3).  This submission includes reads tagged with the sequence AGATCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474425">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474425</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581185</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458905</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_3#2" accession="ERX1415564" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415564</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_3#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_3#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458906, constructed from sample accession ERS474434 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_3).  This submission includes reads tagged with the sequence AGCAGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474434">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474434</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581194</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458906</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_3#3" accession="ERX1415565" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415565</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_3#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_3#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458907, constructed from sample accession ERS474447 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_3).  This submission includes reads tagged with the sequence AGTCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474447">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474447</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581207</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458907</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_3#4" accession="ERX1415566" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415566</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_3#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_3#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458908, constructed from sample accession ERS474455 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_3).  This submission includes reads tagged with the sequence ATCCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474455">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474455</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581215</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458908</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_3#5" accession="ERX1415567" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415567</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_3#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_3#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458909, constructed from sample accession ERS474466 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_3).  This submission includes reads tagged with the sequence ATTGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474466">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474466</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581226</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458909</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_3#6" accession="ERX1415568" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415568</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_3#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_3#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458910, constructed from sample accession ERS474474 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_3).  This submission includes reads tagged with the sequence CAACCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474474">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474474</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581234</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458910</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_3#7" accession="ERX1415569" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415569</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_3#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_3#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458911, constructed from sample accession ERS474485 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_3).  This submission includes reads tagged with the sequence GACTAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474485">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474485</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581245</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458911</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_3#8" accession="ERX1415570" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415570</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_3#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_3#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458912, constructed from sample accession ERS474496 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_3).  This submission includes reads tagged with the sequence CAATGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474496">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474496</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581256</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458912</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_3#9" accession="ERX1415571" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415571</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_3#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_3#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458913, constructed from sample accession ERS474506 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_3).  This submission includes reads tagged with the sequence CACTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474506">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474506</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581266</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458913</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_3#10" accession="ERX1415572" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415572</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_3#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_3#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458914, constructed from sample accession ERS474518 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_3).  This submission includes reads tagged with the sequence CAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474518">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474518</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581278</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458914</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_3#11" accession="ERX1415573" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415573</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_3#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_3#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458915, constructed from sample accession ERS474527 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_3).  This submission includes reads tagged with the sequence CATACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474527">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474527</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581287</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458915</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_3#12" accession="ERX1415574" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415574</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_3#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_3#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458916, constructed from sample accession ERS474539 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_3).  This submission includes reads tagged with the sequence CCAGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474539">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474539</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581299</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458916</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_4#1" accession="ERX1415575" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415575</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_4#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_4#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458917, constructed from sample accession ERS474426 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_4).  This submission includes reads tagged with the sequence CCGAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474426">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474426</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581186</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458917</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_4#2" accession="ERX1415576" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415576</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_4#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_4#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458918, constructed from sample accession ERS474435 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_4).  This submission includes reads tagged with the sequence CCGTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474435">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474435</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581195</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458918</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_4#3" accession="ERX1415577" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415577</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_4#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_4#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458919, constructed from sample accession ERS474448 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_4).  This submission includes reads tagged with the sequence CCTCCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474448">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474448</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581208</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458919</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_4#4" accession="ERX1415578" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415578</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_4#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_4#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458920, constructed from sample accession ERS474456 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_4).  This submission includes reads tagged with the sequence CGAACTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474456">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474456</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581216</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458920</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_4#5" accession="ERX1415579" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415579</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_4#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_4#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458921, constructed from sample accession ERS474467 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_4).  This submission includes reads tagged with the sequence CGACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474467">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474467</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581227</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458921</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_4#6" accession="ERX1415580" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415580</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_4#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_4#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458922, constructed from sample accession ERS474475 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_4).  This submission includes reads tagged with the sequence CGCATAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474475">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474475</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581235</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458922</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_4#7" accession="ERX1415581" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415581</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_4#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_4#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458923, constructed from sample accession ERS474486 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_4).  This submission includes reads tagged with the sequence CTCAATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474486">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474486</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581246</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458923</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_4#8" accession="ERX1415582" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415582</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_4#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_4#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458924, constructed from sample accession ERS474497 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_4).  This submission includes reads tagged with the sequence CTGAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474497">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474497</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581257</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458924</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_4#9" accession="ERX1415583" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415583</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_4#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_4#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458925, constructed from sample accession ERS474508 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_4).  This submission includes reads tagged with the sequence CTGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474508">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474508</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581268</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458925</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_4#10" accession="ERX1415584" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415584</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_4#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_4#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458926, constructed from sample accession ERS474519 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_4).  This submission includes reads tagged with the sequence GAATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474519">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474519</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581279</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458926</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_4#11" accession="ERX1415585" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415585</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_4#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_4#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458927, constructed from sample accession ERS474528 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_4).  This submission includes reads tagged with the sequence CAAGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474528">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474528</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581288</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458927</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_4#12" accession="ERX1415586" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415586</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_4#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_4#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458928, constructed from sample accession ERS474540 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_4).  This submission includes reads tagged with the sequence GAGCTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474540">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474540</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581300</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458928</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_5#1" accession="ERX1415587" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415587</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_5#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_5#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458929, constructed from sample accession ERS474427 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_5).  This submission includes reads tagged with the sequence GATAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474427">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474427</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581187</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458929</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_5#2" accession="ERX1415588" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415588</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_5#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_5#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458930, constructed from sample accession ERS474440 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_5).  This submission includes reads tagged with the sequence GCCACAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474440">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474440</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581200</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458930</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_5#3" accession="ERX1415589" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415589</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_5#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_5#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458931, constructed from sample accession ERS474449 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_5).  This submission includes reads tagged with the sequence GCGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474449">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474449</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581209</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458931</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_5#4" accession="ERX1415590" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415590</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_5#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_5#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458932, constructed from sample accession ERS474457 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_5).  This submission includes reads tagged with the sequence GCTAACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474457">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474457</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581217</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458932</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_5#5" accession="ERX1415591" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415591</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_5#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_5#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458933, constructed from sample accession ERS474468 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_5).  This submission includes reads tagged with the sequence GCTCGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474468">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474468</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581228</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458933</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_5#6" accession="ERX1415592" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415592</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_5#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_5#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458934, constructed from sample accession ERS474477 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_5).  This submission includes reads tagged with the sequence GGAGAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474477">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474477</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581237</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458934</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_5#7" accession="ERX1415593" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415593</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_5#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_5#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458935, constructed from sample accession ERS474488 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_5).  This submission includes reads tagged with the sequence GGTGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474488">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474488</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581248</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458935</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_5#8" accession="ERX1415594" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415594</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_5#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_5#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458936, constructed from sample accession ERS474498 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_5).  This submission includes reads tagged with the sequence GTACGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474498">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474498</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581258</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458936</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_5#9" accession="ERX1415595" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415595</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_5#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_5#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458937, constructed from sample accession ERS474510 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_5).  This submission includes reads tagged with the sequence GTCGTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474510">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474510</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581270</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458937</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_5#10" accession="ERX1415596" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415596</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_5#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_5#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458938, constructed from sample accession ERS474521 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_5).  This submission includes reads tagged with the sequence GTCTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474521">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474521</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581281</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458938</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_5#11" accession="ERX1415597" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415597</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_5#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_5#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458939, constructed from sample accession ERS474529 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_5).  This submission includes reads tagged with the sequence GTGTTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474529">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474529</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581289</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458939</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_5#12" accession="ERX1415598" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415598</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_5#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_5#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458940, constructed from sample accession ERS474541 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_5).  This submission includes reads tagged with the sequence TAGGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474541">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474541</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581301</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458940</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_6#1" accession="ERX1415599" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415599</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_6#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_6#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458941, constructed from sample accession ERS474428 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_6).  This submission includes reads tagged with the sequence TATCAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474428">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474428</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581188</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458941</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_6#2" accession="ERX1415600" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415600</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_6#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_6#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458942, constructed from sample accession ERS474441 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_6).  This submission includes reads tagged with the sequence TCCGTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474441">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474441</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581201</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458942</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_6#3" accession="ERX1415601" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415601</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_6#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_6#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458943, constructed from sample accession ERS474450 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_6).  This submission includes reads tagged with the sequence TCTTCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474450">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474450</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581210</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458943</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_6#4" accession="ERX1415602" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415602</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_6#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_6#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458944, constructed from sample accession ERS474458 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_6).  This submission includes reads tagged with the sequence TGAAGAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474458">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474458</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581218</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458944</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_6#5" accession="ERX1415603" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415603</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_6#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_6#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458945, constructed from sample accession ERS474469 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_6).  This submission includes reads tagged with the sequence TGGAACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474469">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474469</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581229</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458945</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_6#6" accession="ERX1415604" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415604</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_6#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_6#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458946, constructed from sample accession ERS474478 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_6).  This submission includes reads tagged with the sequence TGGCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474478">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474478</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581238</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458946</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_6#7" accession="ERX1415605" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415605</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_6#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_6#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458947, constructed from sample accession ERS474489 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_6).  This submission includes reads tagged with the sequence TGGTGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474489">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474489</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581249</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458947</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_6#8" accession="ERX1415606" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415606</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_6#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_6#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458948, constructed from sample accession ERS474499 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_6).  This submission includes reads tagged with the sequence TTCACGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474499">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474499</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581259</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458948</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_6#9" accession="ERX1415607" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415607</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_6#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_6#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458949, constructed from sample accession ERS474512 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_6).  This submission includes reads tagged with the sequence AACTCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474512">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474512</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581272</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458949</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_6#10" accession="ERX1415608" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415608</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_6#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_6#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458950, constructed from sample accession ERS474522 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_6).  This submission includes reads tagged with the sequence AAGAGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474522">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474522</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581282</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458950</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_6#11" accession="ERX1415609" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415609</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_6#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_6#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458951, constructed from sample accession ERS474530 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_6).  This submission includes reads tagged with the sequence AAGGACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474530">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474530</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581290</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458951</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_6#12" accession="ERX1415610" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415610</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_6#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_6#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458952, constructed from sample accession ERS474542 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_6).  This submission includes reads tagged with the sequence AATCCGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474542">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474542</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581302</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458952</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_7#1" accession="ERX1415611" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415611</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_7#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_7#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458953, constructed from sample accession ERS474429 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_7).  This submission includes reads tagged with the sequence AATGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474429">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474429</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581189</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458953</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_7#2" accession="ERX1415612" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415612</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_7#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_7#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458954, constructed from sample accession ERS474442 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_7).  This submission includes reads tagged with the sequence ACACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474442">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474442</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581202</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458954</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_7#3" accession="ERX1415613" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415613</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_7#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_7#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458955, constructed from sample accession ERS474451 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_7).  This submission includes reads tagged with the sequence ACAGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474451">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474451</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581211</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458955</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_7#4" accession="ERX1415614" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415614</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_7#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_7#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458956, constructed from sample accession ERS474459 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_7).  This submission includes reads tagged with the sequence AGATGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474459">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474459</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581219</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458956</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_7#5" accession="ERX1415615" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415615</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_7#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_7#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458957, constructed from sample accession ERS474470 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_7).  This submission includes reads tagged with the sequence AGCACCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474470">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474470</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581230</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458957</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_7#6" accession="ERX1415616" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415616</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_7#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_7#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458958, constructed from sample accession ERS474479 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_7).  This submission includes reads tagged with the sequence AGCCATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474479">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474479</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581239</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458958</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_7#7" accession="ERX1415617" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415617</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_7#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_7#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458959, constructed from sample accession ERS474492 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_7).  This submission includes reads tagged with the sequence AGGCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474492">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474492</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581252</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458959</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_7#8" accession="ERX1415618" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415618</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_7#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_7#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458960, constructed from sample accession ERS474500 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_7).  This submission includes reads tagged with the sequence ATAGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474500">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474500</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581260</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458960</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_7#9" accession="ERX1415619" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415619</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_7#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_7#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458961, constructed from sample accession ERS474513 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_7).  This submission includes reads tagged with the sequence ATCATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474513">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474513</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581273</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458961</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_7#10" accession="ERX1415620" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415620</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_7#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_7#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458962, constructed from sample accession ERS474523 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_7).  This submission includes reads tagged with the sequence ATTGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474523">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474523</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581283</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458962</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_7#11" accession="ERX1415621" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415621</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_7#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_7#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458963, constructed from sample accession ERS474531 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_7).  This submission includes reads tagged with the sequence CAAGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474531">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474531</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581291</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458963</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_7#12" accession="ERX1415622" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415622</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_7#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_7#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458964, constructed from sample accession ERS474543 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_7).  This submission includes reads tagged with the sequence CACCTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474543">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474543</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581303</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458964</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_8#1" accession="ERX1415623" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415623</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_8#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_8#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458965, constructed from sample accession ERS474430 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_8).  This submission includes reads tagged with the sequence CCATCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474430">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474430</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581190</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458965</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_8#2" accession="ERX1415624" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415624</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_8#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_8#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458966, constructed from sample accession ERS474443 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_8).  This submission includes reads tagged with the sequence CCGACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474443">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474443</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581203</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458966</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_8#3" accession="ERX1415625" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415625</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_8#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_8#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458967, constructed from sample accession ERS474452 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_8).  This submission includes reads tagged with the sequence CCTAATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474452">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474452</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581212</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458967</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_8#4" accession="ERX1415626" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415626</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_8#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_8#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458968, constructed from sample accession ERS474463 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_8).  This submission includes reads tagged with the sequence CCTCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474463">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474463</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581223</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458968</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_8#5" accession="ERX1415627" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415627</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_8#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_8#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458969, constructed from sample accession ERS474471 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_8).  This submission includes reads tagged with the sequence CGACACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474471">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474471</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581231</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458969</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_8#6" accession="ERX1415628" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415628</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_8#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_8#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458970, constructed from sample accession ERS474480 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_8).  This submission includes reads tagged with the sequence CGGATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474480">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474480</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581240</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458970</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_8#7" accession="ERX1415629" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415629</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_8#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_8#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458971, constructed from sample accession ERS474493 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_8).  This submission includes reads tagged with the sequence CTAAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474493">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474493</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581253</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458971</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_8#8" accession="ERX1415630" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415630</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_8#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_8#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458972, constructed from sample accession ERS474502 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_8).  This submission includes reads tagged with the sequence GAACAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474502">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474502</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581262</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458972</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_8#9" accession="ERX1415631" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415631</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_8#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_8#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458973, constructed from sample accession ERS474514 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_8).  This submission includes reads tagged with the sequence GACAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474514">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474514</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581274</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458973</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_8#10" accession="ERX1415632" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415632</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_8#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_8#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458974, constructed from sample accession ERS474524 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_8).  This submission includes reads tagged with the sequence GAGTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474524">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474524</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581284</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458974</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_8#11" accession="ERX1415633" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415633</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_8#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_8#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458975, constructed from sample accession ERS474532 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_8).  This submission includes reads tagged with the sequence GATGAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474532">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474532</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581292</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458975</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18649_8#12" accession="ERX1415634" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415634</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18649_8#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18649_8#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15458976, constructed from sample accession ERS474544 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18649_8).  This submission includes reads tagged with the sequence GCCAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474544">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474544</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581304</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15458976</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_1#1" accession="ERX1415635" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415635</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362686, constructed from sample accession ERS474274 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_1).  This submission includes reads tagged with the sequence AACAACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474274">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474274</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581034</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362686</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_1#2" accession="ERX1415636" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415636</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362687, constructed from sample accession ERS474284 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_1).  This submission includes reads tagged with the sequence AACCGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474284">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474284</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581044</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362687</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_1#3" accession="ERX1415637" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415637</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362688, constructed from sample accession ERS474303 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_1).  This submission includes reads tagged with the sequence AACGCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474303">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474303</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581063</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362688</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_1#4" accession="ERX1415638" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415638</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362689, constructed from sample accession ERS474312 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_1).  This submission includes reads tagged with the sequence AAGACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474312">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474312</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581072</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362689</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_1#5" accession="ERX1415639" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415639</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362690, constructed from sample accession ERS474328 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_1).  This submission includes reads tagged with the sequence AAGGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474328">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474328</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581088</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362690</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_1#6" accession="ERX1415640" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415640</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_1#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_1#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362691, constructed from sample accession ERS474338 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_1).  This submission includes reads tagged with the sequence ACACAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474338">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474338</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581098</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362691</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_1#7" accession="ERX1415641" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415641</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362692, constructed from sample accession ERS474347 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_1).  This submission includes reads tagged with the sequence ACAGCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474347">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581107</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362692</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_1#8" accession="ERX1415642" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415642</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_1#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_1#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362693, constructed from sample accession ERS474359 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_1).  This submission includes reads tagged with the sequence ACCTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474359">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474359</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581119</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362693</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_1#9" accession="ERX1415643" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415643</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_1#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_1#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362694, constructed from sample accession ERS474369 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_1).  This submission includes reads tagged with the sequence ACGCTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474369">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474369</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581129</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362694</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_1#10" accession="ERX1415644" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415644</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_1#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_1#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362695, constructed from sample accession ERS474377 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_1).  This submission includes reads tagged with the sequence ACGTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474377">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474377</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581137</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362695</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_1#11" accession="ERX1415645" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415645</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_1#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_1#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362696, constructed from sample accession ERS474393 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_1).  This submission includes reads tagged with the sequence ACTATGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474393">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474393</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581153</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362696</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_1#12" accession="ERX1415646" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415646</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_1#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_1#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362697, constructed from sample accession ERS474415 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_1).  This submission includes reads tagged with the sequence AGAGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474415">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474415</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581175</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362697</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_2#1" accession="ERX1415647" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415647</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362686, constructed from sample accession ERS474274 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_2).  This submission includes reads tagged with the sequence AACAACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474274">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474274</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581034</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362686</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_2#2" accession="ERX1415648" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415648</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362687, constructed from sample accession ERS474284 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_2).  This submission includes reads tagged with the sequence AACCGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474284">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474284</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581044</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362687</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_2#3" accession="ERX1415649" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415649</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362688, constructed from sample accession ERS474303 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_2).  This submission includes reads tagged with the sequence AACGCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474303">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474303</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581063</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362688</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_2#4" accession="ERX1415650" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415650</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362689, constructed from sample accession ERS474312 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_2).  This submission includes reads tagged with the sequence AAGACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474312">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474312</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581072</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362689</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_2#5" accession="ERX1415651" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415651</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362690, constructed from sample accession ERS474328 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_2).  This submission includes reads tagged with the sequence AAGGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474328">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474328</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581088</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362690</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_2#6" accession="ERX1415652" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415652</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362691, constructed from sample accession ERS474338 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_2).  This submission includes reads tagged with the sequence ACACAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474338">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474338</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581098</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362691</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_2#7" accession="ERX1415653" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415653</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_2#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_2#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362692, constructed from sample accession ERS474347 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_2).  This submission includes reads tagged with the sequence ACAGCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474347">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581107</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362692</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_2#8" accession="ERX1415654" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415654</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_2#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_2#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362693, constructed from sample accession ERS474359 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_2).  This submission includes reads tagged with the sequence ACCTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474359">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474359</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581119</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362693</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_2#9" accession="ERX1415655" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415655</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_2#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_2#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362694, constructed from sample accession ERS474369 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_2).  This submission includes reads tagged with the sequence ACGCTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474369">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474369</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581129</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362694</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_2#10" accession="ERX1415656" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415656</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_2#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_2#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362695, constructed from sample accession ERS474377 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_2).  This submission includes reads tagged with the sequence ACGTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474377">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474377</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581137</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362695</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_2#11" accession="ERX1415657" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415657</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_2#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_2#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362696, constructed from sample accession ERS474393 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_2).  This submission includes reads tagged with the sequence ACTATGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474393">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474393</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581153</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362696</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_2#12" accession="ERX1415658" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415658</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_2#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_2#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362697, constructed from sample accession ERS474415 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_2).  This submission includes reads tagged with the sequence AGAGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474415">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474415</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581175</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362697</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_3#1" accession="ERX1415659" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415659</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_3#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_3#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362686, constructed from sample accession ERS474274 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_3).  This submission includes reads tagged with the sequence AACAACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474274">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474274</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581034</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362686</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_3#2" accession="ERX1415660" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415660</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_3#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_3#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362687, constructed from sample accession ERS474284 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_3).  This submission includes reads tagged with the sequence AACCGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474284">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474284</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581044</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362687</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_3#3" accession="ERX1415661" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415661</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_3#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_3#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362688, constructed from sample accession ERS474303 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_3).  This submission includes reads tagged with the sequence AACGCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474303">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474303</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581063</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362688</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_3#4" accession="ERX1415662" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415662</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_3#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_3#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362689, constructed from sample accession ERS474312 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_3).  This submission includes reads tagged with the sequence AAGACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474312">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474312</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581072</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362689</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_3#5" accession="ERX1415663" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415663</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_3#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_3#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362690, constructed from sample accession ERS474328 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_3).  This submission includes reads tagged with the sequence AAGGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474328">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474328</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581088</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362690</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_3#6" accession="ERX1415664" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415664</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_3#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_3#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362691, constructed from sample accession ERS474338 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_3).  This submission includes reads tagged with the sequence ACACAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474338">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474338</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581098</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362691</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_3#7" accession="ERX1415665" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415665</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_3#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_3#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362692, constructed from sample accession ERS474347 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_3).  This submission includes reads tagged with the sequence ACAGCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474347">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581107</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362692</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_3#8" accession="ERX1415666" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415666</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_3#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_3#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362693, constructed from sample accession ERS474359 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_3).  This submission includes reads tagged with the sequence ACCTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474359">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474359</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581119</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362693</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_3#9" accession="ERX1415667" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415667</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_3#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_3#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362694, constructed from sample accession ERS474369 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_3).  This submission includes reads tagged with the sequence ACGCTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474369">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474369</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581129</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362694</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_3#10" accession="ERX1415668" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415668</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_3#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_3#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362695, constructed from sample accession ERS474377 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_3).  This submission includes reads tagged with the sequence ACGTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474377">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474377</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581137</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362695</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_3#11" accession="ERX1415669" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415669</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_3#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_3#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362696, constructed from sample accession ERS474393 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_3).  This submission includes reads tagged with the sequence ACTATGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474393">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474393</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581153</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362696</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_3#12" accession="ERX1415670" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415670</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_3#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_3#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362697, constructed from sample accession ERS474415 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_3).  This submission includes reads tagged with the sequence AGAGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474415">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474415</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581175</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362697</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_4#1" accession="ERX1415671" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415671</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_4#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_4#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362686, constructed from sample accession ERS474274 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_4).  This submission includes reads tagged with the sequence AACAACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474274">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474274</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581034</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362686</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_4#2" accession="ERX1415672" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415672</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_4#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_4#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362687, constructed from sample accession ERS474284 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_4).  This submission includes reads tagged with the sequence AACCGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474284">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474284</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581044</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362687</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_4#3" accession="ERX1415673" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415673</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_4#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_4#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362688, constructed from sample accession ERS474303 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_4).  This submission includes reads tagged with the sequence AACGCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474303">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474303</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581063</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362688</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_4#4" accession="ERX1415674" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415674</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_4#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_4#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362689, constructed from sample accession ERS474312 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_4).  This submission includes reads tagged with the sequence AAGACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474312">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474312</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581072</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362689</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_4#5" accession="ERX1415675" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415675</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_4#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_4#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362690, constructed from sample accession ERS474328 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_4).  This submission includes reads tagged with the sequence AAGGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474328">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474328</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581088</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362690</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_4#6" accession="ERX1415676" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415676</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_4#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_4#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362691, constructed from sample accession ERS474338 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_4).  This submission includes reads tagged with the sequence ACACAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474338">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474338</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581098</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362691</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_4#7" accession="ERX1415677" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415677</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_4#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_4#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362692, constructed from sample accession ERS474347 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_4).  This submission includes reads tagged with the sequence ACAGCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474347">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581107</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362692</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_4#8" accession="ERX1415678" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415678</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_4#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_4#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362693, constructed from sample accession ERS474359 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_4).  This submission includes reads tagged with the sequence ACCTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474359">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474359</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581119</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362693</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_4#9" accession="ERX1415679" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415679</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_4#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_4#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362694, constructed from sample accession ERS474369 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_4).  This submission includes reads tagged with the sequence ACGCTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474369">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474369</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581129</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362694</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_4#10" accession="ERX1415680" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415680</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_4#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_4#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362695, constructed from sample accession ERS474377 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_4).  This submission includes reads tagged with the sequence ACGTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474377">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474377</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581137</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362695</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_4#11" accession="ERX1415681" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415681</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_4#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_4#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362696, constructed from sample accession ERS474393 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_4).  This submission includes reads tagged with the sequence ACTATGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474393">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474393</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581153</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362696</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_4#12" accession="ERX1415682" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415682</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_4#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_4#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362697, constructed from sample accession ERS474415 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_4).  This submission includes reads tagged with the sequence AGAGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474415">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474415</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581175</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362697</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_5#1" accession="ERX1415683" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415683</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_5#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_5#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362686, constructed from sample accession ERS474274 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_5).  This submission includes reads tagged with the sequence AACAACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474274">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474274</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581034</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362686</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_5#2" accession="ERX1415684" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415684</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_5#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_5#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362687, constructed from sample accession ERS474284 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_5).  This submission includes reads tagged with the sequence AACCGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474284">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474284</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581044</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362687</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_5#3" accession="ERX1415685" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415685</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_5#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_5#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362688, constructed from sample accession ERS474303 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_5).  This submission includes reads tagged with the sequence AACGCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474303">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474303</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581063</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362688</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_5#4" accession="ERX1415686" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415686</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_5#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_5#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362689, constructed from sample accession ERS474312 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_5).  This submission includes reads tagged with the sequence AAGACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474312">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474312</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581072</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362689</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_5#5" accession="ERX1415687" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415687</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_5#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_5#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362690, constructed from sample accession ERS474328 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_5).  This submission includes reads tagged with the sequence AAGGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474328">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474328</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581088</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362690</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_5#6" accession="ERX1415688" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415688</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_5#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_5#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362691, constructed from sample accession ERS474338 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_5).  This submission includes reads tagged with the sequence ACACAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474338">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474338</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581098</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362691</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_5#7" accession="ERX1415689" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415689</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_5#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_5#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362692, constructed from sample accession ERS474347 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_5).  This submission includes reads tagged with the sequence ACAGCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474347">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581107</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362692</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_5#8" accession="ERX1415690" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415690</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_5#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_5#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362693, constructed from sample accession ERS474359 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_5).  This submission includes reads tagged with the sequence ACCTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474359">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474359</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581119</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362693</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_5#9" accession="ERX1415691" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415691</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_5#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_5#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362694, constructed from sample accession ERS474369 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_5).  This submission includes reads tagged with the sequence ACGCTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474369">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474369</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581129</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362694</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_5#10" accession="ERX1415692" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415692</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_5#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_5#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362695, constructed from sample accession ERS474377 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_5).  This submission includes reads tagged with the sequence ACGTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474377">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474377</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581137</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362695</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_5#11" accession="ERX1415693" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415693</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_5#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_5#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362696, constructed from sample accession ERS474393 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_5).  This submission includes reads tagged with the sequence ACTATGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474393">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474393</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581153</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362696</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_5#12" accession="ERX1415694" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415694</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_5#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_5#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362697, constructed from sample accession ERS474415 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_5).  This submission includes reads tagged with the sequence AGAGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474415">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474415</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581175</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362697</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_6#1" accession="ERX1415695" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415695</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_6#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_6#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362686, constructed from sample accession ERS474274 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_6).  This submission includes reads tagged with the sequence AACAACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474274">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474274</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581034</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362686</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_6#2" accession="ERX1415696" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415696</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_6#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_6#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362687, constructed from sample accession ERS474284 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_6).  This submission includes reads tagged with the sequence AACCGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474284">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474284</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581044</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362687</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_6#3" accession="ERX1415697" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415697</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_6#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_6#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362688, constructed from sample accession ERS474303 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_6).  This submission includes reads tagged with the sequence AACGCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474303">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474303</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581063</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362688</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_6#4" accession="ERX1415698" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415698</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_6#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_6#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362689, constructed from sample accession ERS474312 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_6).  This submission includes reads tagged with the sequence AAGACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474312">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474312</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581072</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362689</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_6#5" accession="ERX1415699" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415699</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_6#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_6#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362690, constructed from sample accession ERS474328 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_6).  This submission includes reads tagged with the sequence AAGGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474328">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474328</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581088</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362690</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_6#6" accession="ERX1415700" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415700</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_6#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_6#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362691, constructed from sample accession ERS474338 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_6).  This submission includes reads tagged with the sequence ACACAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474338">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474338</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581098</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362691</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_6#7" accession="ERX1415701" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415701</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_6#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_6#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362692, constructed from sample accession ERS474347 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_6).  This submission includes reads tagged with the sequence ACAGCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474347">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581107</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362692</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_6#8" accession="ERX1415702" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415702</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_6#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_6#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362693, constructed from sample accession ERS474359 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_6).  This submission includes reads tagged with the sequence ACCTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474359">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474359</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581119</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362693</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_6#9" accession="ERX1415703" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415703</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_6#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_6#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362694, constructed from sample accession ERS474369 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_6).  This submission includes reads tagged with the sequence ACGCTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474369">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474369</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581129</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362694</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_6#10" accession="ERX1415704" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415704</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_6#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_6#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362695, constructed from sample accession ERS474377 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_6).  This submission includes reads tagged with the sequence ACGTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474377">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474377</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581137</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362695</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_6#11" accession="ERX1415705" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415705</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_6#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_6#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362696, constructed from sample accession ERS474393 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_6).  This submission includes reads tagged with the sequence ACTATGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474393">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474393</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581153</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362696</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_6#12" accession="ERX1415706" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415706</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_6#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_6#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362697, constructed from sample accession ERS474415 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_6).  This submission includes reads tagged with the sequence AGAGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474415">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474415</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581175</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362697</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_7#1" accession="ERX1415707" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415707</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_7#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_7#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362686, constructed from sample accession ERS474274 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_7).  This submission includes reads tagged with the sequence AACAACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474274">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474274</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581034</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362686</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_7#2" accession="ERX1415708" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415708</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_7#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_7#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362687, constructed from sample accession ERS474284 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_7).  This submission includes reads tagged with the sequence AACCGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474284">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474284</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581044</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362687</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_7#3" accession="ERX1415709" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415709</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_7#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_7#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362688, constructed from sample accession ERS474303 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_7).  This submission includes reads tagged with the sequence AACGCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474303">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474303</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581063</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362688</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_7#4" accession="ERX1415710" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415710</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_7#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_7#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362689, constructed from sample accession ERS474312 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_7).  This submission includes reads tagged with the sequence AAGACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474312">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474312</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581072</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362689</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_7#5" accession="ERX1415711" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415711</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_7#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_7#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362690, constructed from sample accession ERS474328 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_7).  This submission includes reads tagged with the sequence AAGGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474328">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474328</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581088</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362690</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_7#6" accession="ERX1415712" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415712</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_7#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_7#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362691, constructed from sample accession ERS474338 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_7).  This submission includes reads tagged with the sequence ACACAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474338">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474338</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581098</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362691</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_7#7" accession="ERX1415713" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415713</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_7#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_7#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362692, constructed from sample accession ERS474347 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_7).  This submission includes reads tagged with the sequence ACAGCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474347">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581107</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362692</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_7#8" accession="ERX1415714" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415714</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_7#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_7#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362693, constructed from sample accession ERS474359 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_7).  This submission includes reads tagged with the sequence ACCTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474359">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474359</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581119</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362693</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_7#9" accession="ERX1415715" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415715</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_7#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_7#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362694, constructed from sample accession ERS474369 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_7).  This submission includes reads tagged with the sequence ACGCTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474369">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474369</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581129</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362694</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_7#10" accession="ERX1415716" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415716</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_7#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_7#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362695, constructed from sample accession ERS474377 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_7).  This submission includes reads tagged with the sequence ACGTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474377">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474377</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581137</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362695</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_7#11" accession="ERX1415717" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415717</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_7#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_7#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362696, constructed from sample accession ERS474393 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_7).  This submission includes reads tagged with the sequence ACTATGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474393">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474393</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581153</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362696</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_7#12" accession="ERX1415718" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415718</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_7#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_7#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362697, constructed from sample accession ERS474415 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_7).  This submission includes reads tagged with the sequence AGAGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474415">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474415</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581175</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362697</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_8#1" accession="ERX1415719" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415719</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_8#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_8#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362686, constructed from sample accession ERS474274 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_8).  This submission includes reads tagged with the sequence AACAACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474274">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474274</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581034</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362686</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_8#2" accession="ERX1415720" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415720</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_8#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_8#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362687, constructed from sample accession ERS474284 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_8).  This submission includes reads tagged with the sequence AACCGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474284">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474284</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581044</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362687</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_8#3" accession="ERX1415721" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415721</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_8#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_8#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362688, constructed from sample accession ERS474303 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_8).  This submission includes reads tagged with the sequence AACGCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474303">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474303</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581063</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362688</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_8#4" accession="ERX1415722" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415722</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_8#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_8#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362689, constructed from sample accession ERS474312 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_8).  This submission includes reads tagged with the sequence AAGACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474312">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474312</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581072</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362689</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_8#5" accession="ERX1415723" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415723</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_8#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_8#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362690, constructed from sample accession ERS474328 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_8).  This submission includes reads tagged with the sequence AAGGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474328">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474328</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581088</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362690</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_8#6" accession="ERX1415724" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415724</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_8#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_8#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362691, constructed from sample accession ERS474338 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_8).  This submission includes reads tagged with the sequence ACACAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474338">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474338</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581098</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362691</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_8#7" accession="ERX1415725" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415725</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_8#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_8#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362692, constructed from sample accession ERS474347 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_8).  This submission includes reads tagged with the sequence ACAGCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474347">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581107</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362692</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_8#8" accession="ERX1415726" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415726</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_8#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_8#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362693, constructed from sample accession ERS474359 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_8).  This submission includes reads tagged with the sequence ACCTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474359">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474359</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581119</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362693</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_8#9" accession="ERX1415727" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415727</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_8#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_8#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362694, constructed from sample accession ERS474369 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_8).  This submission includes reads tagged with the sequence ACGCTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474369">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474369</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581129</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362694</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_8#10" accession="ERX1415728" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415728</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_8#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_8#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362695, constructed from sample accession ERS474377 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_8).  This submission includes reads tagged with the sequence ACGTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474377">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474377</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581137</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362695</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_8#11" accession="ERX1415729" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415729</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_8#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_8#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362696, constructed from sample accession ERS474393 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_8).  This submission includes reads tagged with the sequence ACTATGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474393">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474393</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581153</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362696</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18650_8#12" accession="ERX1415730" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415730</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18650_8#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18650_8#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362697, constructed from sample accession ERS474415 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18650_8).  This submission includes reads tagged with the sequence AGAGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474415">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474415</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581175</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362697</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_1#1" accession="ERX1415731" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415731</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362674, constructed from sample accession ERS474273 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_1).  This submission includes reads tagged with the sequence AACGTGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474273">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474273</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581033</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362674</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="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_1#2" accession="ERX1415732" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415732</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362675, constructed from sample accession ERS474282 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_1).  This submission includes reads tagged with the sequence AAACATCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474282">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474282</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581042</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362675</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="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_1#3" accession="ERX1415733" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415733</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362676, constructed from sample accession ERS474302 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_1).  This submission includes reads tagged with the sequence ATGCCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474302">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474302</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581062</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362676</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="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_1#4" accession="ERX1415734" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415734</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362677, constructed from sample accession ERS474311 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_1).  This submission includes reads tagged with the sequence AGTGGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474311">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474311</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581071</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362677</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="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_1#5" accession="ERX1415735" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415735</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362678, constructed from sample accession ERS474326 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_1).  This submission includes reads tagged with the sequence ACCACTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474326">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474326</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581086</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362678</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="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_1#6" accession="ERX1415736" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415736</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_1#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_1#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362679, constructed from sample accession ERS474337 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_1).  This submission includes reads tagged with the sequence ACATTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474337">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474337</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581097</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362679</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="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_1#7" accession="ERX1415737" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415737</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362680, constructed from sample accession ERS474345 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_1).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474345">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474345</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581105</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362680</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="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_1#8" accession="ERX1415738" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415738</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_1#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_1#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362681, constructed from sample accession ERS474358 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_1).  This submission includes reads tagged with the sequence CATCAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474358">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474358</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581118</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362681</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="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_1#9" accession="ERX1415739" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415739</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_1#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_1#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362682, constructed from sample accession ERS474368 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_1).  This submission includes reads tagged with the sequence CGCTGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474368">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474368</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581128</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362682</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="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_1#10" accession="ERX1415740" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415740</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_1#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_1#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362683, constructed from sample accession ERS474376 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_1).  This submission includes reads tagged with the sequence ACAAGCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474376">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474376</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581136</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362683</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="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_1#11" accession="ERX1415741" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415741</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_1#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_1#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362684, constructed from sample accession ERS474391 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_1).  This submission includes reads tagged with the sequence CTGTAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474391">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474391</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581151</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362684</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="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_1#12" accession="ERX1415742" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415742</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_1#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_1#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362685, constructed from sample accession ERS474404 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_1).  This submission includes reads tagged with the sequence AGTACAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474404">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474404</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581164</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362685</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="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_5#1" accession="ERX1415743" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415743</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_5#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_5#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362674, constructed from sample accession ERS474273 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_5).  This submission includes reads tagged with the sequence AACGTGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474273">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474273</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581033</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362674</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_5#2" accession="ERX1415744" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415744</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_5#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_5#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362675, constructed from sample accession ERS474282 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_5).  This submission includes reads tagged with the sequence AAACATCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474282">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474282</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581042</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362675</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_5#3" accession="ERX1415745" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415745</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_5#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_5#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362676, constructed from sample accession ERS474302 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_5).  This submission includes reads tagged with the sequence ATGCCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474302">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474302</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581062</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362676</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_5#4" accession="ERX1415746" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415746</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_5#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_5#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362677, constructed from sample accession ERS474311 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_5).  This submission includes reads tagged with the sequence AGTGGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474311">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474311</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581071</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362677</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_5#5" accession="ERX1415747" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415747</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_5#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_5#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362678, constructed from sample accession ERS474326 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_5).  This submission includes reads tagged with the sequence ACCACTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474326">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474326</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581086</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362678</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_5#6" accession="ERX1415748" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415748</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_5#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_5#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362679, constructed from sample accession ERS474337 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_5).  This submission includes reads tagged with the sequence ACATTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474337">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474337</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581097</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362679</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_5#7" accession="ERX1415749" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415749</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_5#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_5#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362680, constructed from sample accession ERS474345 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_5).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474345">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474345</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581105</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362680</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_5#8" accession="ERX1415750" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415750</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_5#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_5#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362681, constructed from sample accession ERS474358 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_5).  This submission includes reads tagged with the sequence CATCAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474358">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474358</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581118</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362681</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_5#9" accession="ERX1415751" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415751</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_5#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_5#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362682, constructed from sample accession ERS474368 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_5).  This submission includes reads tagged with the sequence CGCTGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474368">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474368</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581128</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362682</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_5#10" accession="ERX1415752" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415752</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_5#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_5#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362683, constructed from sample accession ERS474376 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_5).  This submission includes reads tagged with the sequence ACAAGCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474376">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474376</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581136</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362683</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_5#11" accession="ERX1415753" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415753</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_5#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_5#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362684, constructed from sample accession ERS474391 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_5).  This submission includes reads tagged with the sequence CTGTAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474391">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474391</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581151</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362684</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_5#12" accession="ERX1415754" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415754</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_5#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_5#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362685, constructed from sample accession ERS474404 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_5).  This submission includes reads tagged with the sequence AGTACAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474404">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474404</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581164</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362685</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_6#1" accession="ERX1415755" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415755</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_6#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_6#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362674, constructed from sample accession ERS474273 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_6).  This submission includes reads tagged with the sequence AACGTGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474273">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474273</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581033</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362674</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_6#2" accession="ERX1415756" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415756</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_6#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_6#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362675, constructed from sample accession ERS474282 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_6).  This submission includes reads tagged with the sequence AAACATCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474282">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474282</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581042</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362675</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_6#3" accession="ERX1415757" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415757</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_6#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_6#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362676, constructed from sample accession ERS474302 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_6).  This submission includes reads tagged with the sequence ATGCCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474302">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474302</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581062</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362676</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_6#4" accession="ERX1415758" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415758</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_6#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_6#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362677, constructed from sample accession ERS474311 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_6).  This submission includes reads tagged with the sequence AGTGGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474311">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474311</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581071</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362677</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_6#5" accession="ERX1415759" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415759</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_6#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_6#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362678, constructed from sample accession ERS474326 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_6).  This submission includes reads tagged with the sequence ACCACTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474326">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474326</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581086</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362678</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_6#6" accession="ERX1415760" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415760</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_6#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_6#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362679, constructed from sample accession ERS474337 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_6).  This submission includes reads tagged with the sequence ACATTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474337">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474337</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581097</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362679</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_6#7" accession="ERX1415761" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415761</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_6#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_6#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362680, constructed from sample accession ERS474345 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_6).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474345">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474345</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581105</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362680</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_6#8" accession="ERX1415762" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415762</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_6#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_6#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362681, constructed from sample accession ERS474358 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_6).  This submission includes reads tagged with the sequence CATCAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474358">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474358</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581118</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362681</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_6#9" accession="ERX1415763" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415763</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_6#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_6#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362682, constructed from sample accession ERS474368 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_6).  This submission includes reads tagged with the sequence CGCTGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474368">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474368</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581128</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362682</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_6#10" accession="ERX1415764" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415764</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_6#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_6#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362683, constructed from sample accession ERS474376 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_6).  This submission includes reads tagged with the sequence ACAAGCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474376">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474376</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581136</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362683</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_6#11" accession="ERX1415765" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415765</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_6#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_6#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362684, constructed from sample accession ERS474391 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_6).  This submission includes reads tagged with the sequence CTGTAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474391">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474391</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581151</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362684</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_6#12" accession="ERX1415766" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415766</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_6#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_6#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362685, constructed from sample accession ERS474404 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_6).  This submission includes reads tagged with the sequence AGTACAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474404">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474404</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581164</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362685</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_7#1" accession="ERX1415767" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415767</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_7#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_7#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362674, constructed from sample accession ERS474273 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_7).  This submission includes reads tagged with the sequence AACGTGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474273">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474273</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581033</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362674</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_7#2" accession="ERX1415768" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415768</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_7#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_7#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362675, constructed from sample accession ERS474282 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_7).  This submission includes reads tagged with the sequence AAACATCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474282">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474282</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581042</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362675</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_7#3" accession="ERX1415769" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415769</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_7#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_7#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362676, constructed from sample accession ERS474302 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_7).  This submission includes reads tagged with the sequence ATGCCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474302">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474302</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581062</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362676</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_7#4" accession="ERX1415770" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415770</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_7#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_7#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362677, constructed from sample accession ERS474311 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_7).  This submission includes reads tagged with the sequence AGTGGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474311">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474311</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581071</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362677</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_7#5" accession="ERX1415771" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415771</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_7#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_7#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362678, constructed from sample accession ERS474326 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_7).  This submission includes reads tagged with the sequence ACCACTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474326">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474326</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581086</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362678</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_7#6" accession="ERX1415772" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415772</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_7#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_7#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362679, constructed from sample accession ERS474337 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_7).  This submission includes reads tagged with the sequence ACATTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474337">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474337</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581097</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362679</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_7#7" accession="ERX1415773" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415773</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_7#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_7#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362680, constructed from sample accession ERS474345 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_7).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474345">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474345</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581105</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362680</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_7#8" accession="ERX1415774" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415774</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_7#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_7#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362681, constructed from sample accession ERS474358 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_7).  This submission includes reads tagged with the sequence CATCAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474358">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474358</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581118</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362681</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_7#9" accession="ERX1415775" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415775</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_7#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_7#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362682, constructed from sample accession ERS474368 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_7).  This submission includes reads tagged with the sequence CGCTGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474368">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474368</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581128</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362682</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_7#10" accession="ERX1415776" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415776</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_7#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_7#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362683, constructed from sample accession ERS474376 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_7).  This submission includes reads tagged with the sequence ACAAGCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474376">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474376</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581136</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362683</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_7#11" accession="ERX1415777" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415777</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_7#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_7#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362684, constructed from sample accession ERS474391 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_7).  This submission includes reads tagged with the sequence CTGTAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474391">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474391</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581151</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362684</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_7#12" accession="ERX1415778" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415778</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_7#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_7#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362685, constructed from sample accession ERS474404 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_7).  This submission includes reads tagged with the sequence AGTACAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474404">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474404</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581164</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362685</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_8#1" accession="ERX1415779" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415779</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_8#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_8#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362674, constructed from sample accession ERS474273 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_8).  This submission includes reads tagged with the sequence AACGTGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474273">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474273</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581033</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362674</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_8#2" accession="ERX1415780" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415780</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_8#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_8#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362675, constructed from sample accession ERS474282 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_8).  This submission includes reads tagged with the sequence AAACATCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474282">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474282</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581042</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362675</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_8#3" accession="ERX1415781" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415781</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_8#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_8#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362676, constructed from sample accession ERS474302 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_8).  This submission includes reads tagged with the sequence ATGCCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474302">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474302</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581062</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362676</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_8#4" accession="ERX1415782" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415782</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_8#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_8#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362677, constructed from sample accession ERS474311 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_8).  This submission includes reads tagged with the sequence AGTGGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474311">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474311</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581071</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362677</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_8#5" accession="ERX1415783" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415783</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_8#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_8#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362678, constructed from sample accession ERS474326 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_8).  This submission includes reads tagged with the sequence ACCACTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474326">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474326</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581086</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362678</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_8#6" accession="ERX1415784" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415784</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_8#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_8#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362679, constructed from sample accession ERS474337 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_8).  This submission includes reads tagged with the sequence ACATTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474337">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474337</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581097</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362679</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_8#7" accession="ERX1415785" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415785</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_8#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_8#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362680, constructed from sample accession ERS474345 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_8).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474345">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474345</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581105</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362680</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_8#8" accession="ERX1415786" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415786</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_8#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_8#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362681, constructed from sample accession ERS474358 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_8).  This submission includes reads tagged with the sequence CATCAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474358">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474358</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581118</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362681</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_8#9" accession="ERX1415787" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415787</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_8#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_8#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362682, constructed from sample accession ERS474368 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_8).  This submission includes reads tagged with the sequence CGCTGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474368">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474368</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581128</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362682</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_8#10" accession="ERX1415788" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415788</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_8#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_8#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362683, constructed from sample accession ERS474376 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_8).  This submission includes reads tagged with the sequence ACAAGCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474376">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474376</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581136</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362683</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_8#11" accession="ERX1415789" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415789</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_8#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_8#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362684, constructed from sample accession ERS474391 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_8).  This submission includes reads tagged with the sequence CTGTAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474391">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474391</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581151</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362684</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18651_8#12" accession="ERX1415790" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415790</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18651_8#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18651_8#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362685, constructed from sample accession ERS474404 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18651_8).  This submission includes reads tagged with the sequence AGTACAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474404">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474404</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581164</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362685</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_1#1" accession="ERX1415791" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415791</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362710, constructed from sample accession ERS474277 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_1).  This submission includes reads tagged with the sequence CCGAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474277">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474277</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581037</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362710</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_1#2" accession="ERX1415792" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415792</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362711, constructed from sample accession ERS474292 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_1).  This submission includes reads tagged with the sequence CCGTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474292">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474292</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581052</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362711</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_1#3" accession="ERX1415793" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415793</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362712, constructed from sample accession ERS474305 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_1).  This submission includes reads tagged with the sequence CCTCCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474305">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474305</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581065</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362712</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_1#4" accession="ERX1415794" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415794</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362713, constructed from sample accession ERS474316 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_1).  This submission includes reads tagged with the sequence CGAACTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474316">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474316</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581076</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362713</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_1#5" accession="ERX1415795" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415795</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362714, constructed from sample accession ERS474332 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_1).  This submission includes reads tagged with the sequence CGACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474332">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474332</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581092</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362714</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_1#6" accession="ERX1415796" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415796</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_1#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_1#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362715, constructed from sample accession ERS474340 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_1).  This submission includes reads tagged with the sequence CGCATAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474340">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474340</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581100</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362715</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_1#7" accession="ERX1415797" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415797</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362716, constructed from sample accession ERS474349 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_1).  This submission includes reads tagged with the sequence CTCAATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474349">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474349</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581109</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362716</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_1#8" accession="ERX1415798" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415798</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_1#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_1#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362717, constructed from sample accession ERS474362 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_1).  This submission includes reads tagged with the sequence CTGAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474362">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474362</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581122</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362717</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_1#9" accession="ERX1415799" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415799</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_1#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_1#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362718, constructed from sample accession ERS474371 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_1).  This submission includes reads tagged with the sequence CTGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474371">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474371</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581131</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362718</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_1#10" accession="ERX1415800" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415800</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_1#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_1#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362719, constructed from sample accession ERS474385 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_1).  This submission includes reads tagged with the sequence GAATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474385">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474385</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581145</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362719</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_1#11" accession="ERX1415801" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415801</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_1#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_1#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362720, constructed from sample accession ERS474396 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_1).  This submission includes reads tagged with the sequence CAAGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474396">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474396</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581156</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362720</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_1#12" accession="ERX1415802" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415802</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_1#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_1#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362721, constructed from sample accession ERS474418 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_1).  This submission includes reads tagged with the sequence GAGCTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474418">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474418</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581178</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362721</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_2#1" accession="ERX1415803" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415803</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362710, constructed from sample accession ERS474277 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_2).  This submission includes reads tagged with the sequence CCGAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474277">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474277</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581037</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362710</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_2#2" accession="ERX1415804" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415804</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362711, constructed from sample accession ERS474292 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_2).  This submission includes reads tagged with the sequence CCGTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474292">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474292</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581052</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362711</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_2#3" accession="ERX1415805" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415805</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362712, constructed from sample accession ERS474305 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_2).  This submission includes reads tagged with the sequence CCTCCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474305">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474305</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581065</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362712</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_2#4" accession="ERX1415806" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415806</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362713, constructed from sample accession ERS474316 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_2).  This submission includes reads tagged with the sequence CGAACTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474316">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474316</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581076</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362713</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_2#5" accession="ERX1415807" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415807</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362714, constructed from sample accession ERS474332 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_2).  This submission includes reads tagged with the sequence CGACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474332">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474332</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581092</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362714</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_2#6" accession="ERX1415808" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415808</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362715, constructed from sample accession ERS474340 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_2).  This submission includes reads tagged with the sequence CGCATAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474340">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474340</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581100</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362715</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_2#7" accession="ERX1415809" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415809</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_2#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_2#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362716, constructed from sample accession ERS474349 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_2).  This submission includes reads tagged with the sequence CTCAATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474349">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474349</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581109</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362716</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_2#8" accession="ERX1415810" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415810</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_2#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_2#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362717, constructed from sample accession ERS474362 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_2).  This submission includes reads tagged with the sequence CTGAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474362">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474362</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581122</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362717</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_2#9" accession="ERX1415811" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415811</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_2#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_2#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362718, constructed from sample accession ERS474371 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_2).  This submission includes reads tagged with the sequence CTGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474371">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474371</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581131</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362718</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_2#10" accession="ERX1415812" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415812</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_2#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_2#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362719, constructed from sample accession ERS474385 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_2).  This submission includes reads tagged with the sequence GAATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474385">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474385</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581145</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362719</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_2#11" accession="ERX1415813" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415813</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_2#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_2#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362720, constructed from sample accession ERS474396 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_2).  This submission includes reads tagged with the sequence CAAGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474396">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474396</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581156</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362720</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_2#12" accession="ERX1415814" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415814</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_2#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_2#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362721, constructed from sample accession ERS474418 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_2).  This submission includes reads tagged with the sequence GAGCTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474418">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474418</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581178</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362721</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_3#1" accession="ERX1415815" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415815</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_3#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_3#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362710, constructed from sample accession ERS474277 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_3).  This submission includes reads tagged with the sequence CCGAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474277">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474277</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581037</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362710</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_3#2" accession="ERX1415816" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415816</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_3#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_3#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362711, constructed from sample accession ERS474292 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_3).  This submission includes reads tagged with the sequence CCGTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474292">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474292</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581052</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362711</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_3#3" accession="ERX1415817" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415817</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_3#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_3#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362712, constructed from sample accession ERS474305 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_3).  This submission includes reads tagged with the sequence CCTCCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474305">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474305</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581065</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362712</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_3#4" accession="ERX1415818" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415818</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_3#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_3#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362713, constructed from sample accession ERS474316 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_3).  This submission includes reads tagged with the sequence CGAACTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474316">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474316</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581076</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362713</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_3#5" accession="ERX1415819" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415819</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_3#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_3#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362714, constructed from sample accession ERS474332 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_3).  This submission includes reads tagged with the sequence CGACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474332">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474332</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581092</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362714</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_3#6" accession="ERX1415820" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415820</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_3#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_3#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362715, constructed from sample accession ERS474340 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_3).  This submission includes reads tagged with the sequence CGCATAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474340">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474340</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581100</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362715</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_3#7" accession="ERX1415821" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415821</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_3#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_3#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362716, constructed from sample accession ERS474349 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_3).  This submission includes reads tagged with the sequence CTCAATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474349">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474349</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581109</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362716</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_3#8" accession="ERX1415822" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415822</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_3#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_3#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362717, constructed from sample accession ERS474362 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_3).  This submission includes reads tagged with the sequence CTGAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474362">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474362</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581122</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362717</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_3#9" accession="ERX1415823" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415823</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_3#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_3#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362718, constructed from sample accession ERS474371 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_3).  This submission includes reads tagged with the sequence CTGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474371">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474371</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581131</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362718</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_3#10" accession="ERX1415824" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415824</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_3#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_3#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362719, constructed from sample accession ERS474385 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_3).  This submission includes reads tagged with the sequence GAATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474385">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474385</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581145</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362719</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_3#11" accession="ERX1415825" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415825</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_3#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_3#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362720, constructed from sample accession ERS474396 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_3).  This submission includes reads tagged with the sequence CAAGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474396">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474396</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581156</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362720</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_3#12" accession="ERX1415826" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415826</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_3#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_3#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362721, constructed from sample accession ERS474418 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_3).  This submission includes reads tagged with the sequence GAGCTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474418">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474418</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581178</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362721</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_4#1" accession="ERX1415827" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415827</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_4#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_4#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362710, constructed from sample accession ERS474277 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_4).  This submission includes reads tagged with the sequence CCGAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474277">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474277</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581037</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362710</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_4#2" accession="ERX1415828" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415828</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_4#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_4#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362711, constructed from sample accession ERS474292 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_4).  This submission includes reads tagged with the sequence CCGTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474292">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474292</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581052</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362711</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_4#3" accession="ERX1415829" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415829</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_4#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_4#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362712, constructed from sample accession ERS474305 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_4).  This submission includes reads tagged with the sequence CCTCCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474305">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474305</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581065</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362712</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_4#4" accession="ERX1415830" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415830</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_4#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_4#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362713, constructed from sample accession ERS474316 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_4).  This submission includes reads tagged with the sequence CGAACTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474316">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474316</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581076</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362713</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_4#5" accession="ERX1415831" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415831</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_4#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_4#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362714, constructed from sample accession ERS474332 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_4).  This submission includes reads tagged with the sequence CGACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474332">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474332</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581092</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362714</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_4#6" accession="ERX1415832" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415832</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_4#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_4#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362715, constructed from sample accession ERS474340 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_4).  This submission includes reads tagged with the sequence CGCATAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474340">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474340</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581100</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362715</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_4#7" accession="ERX1415833" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415833</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_4#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_4#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362716, constructed from sample accession ERS474349 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_4).  This submission includes reads tagged with the sequence CTCAATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474349">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474349</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581109</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362716</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_4#8" accession="ERX1415834" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415834</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_4#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_4#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362717, constructed from sample accession ERS474362 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_4).  This submission includes reads tagged with the sequence CTGAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474362">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474362</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581122</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362717</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_4#9" accession="ERX1415835" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415835</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_4#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_4#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362718, constructed from sample accession ERS474371 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_4).  This submission includes reads tagged with the sequence CTGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474371">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474371</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581131</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362718</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_4#10" accession="ERX1415836" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415836</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_4#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_4#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362719, constructed from sample accession ERS474385 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_4).  This submission includes reads tagged with the sequence GAATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474385">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474385</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581145</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362719</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_4#11" accession="ERX1415837" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415837</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_4#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_4#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362720, constructed from sample accession ERS474396 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_4).  This submission includes reads tagged with the sequence CAAGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474396">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474396</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581156</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362720</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_4#12" accession="ERX1415838" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415838</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_4#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_4#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362721, constructed from sample accession ERS474418 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_4).  This submission includes reads tagged with the sequence GAGCTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474418">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474418</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581178</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362721</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_5#1" accession="ERX1415839" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415839</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_5#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_5#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362710, constructed from sample accession ERS474277 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_5).  This submission includes reads tagged with the sequence CCGAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474277">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474277</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581037</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362710</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_5#2" accession="ERX1415840" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415840</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_5#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_5#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362711, constructed from sample accession ERS474292 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_5).  This submission includes reads tagged with the sequence CCGTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474292">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474292</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581052</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362711</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_5#3" accession="ERX1415841" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415841</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_5#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_5#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362712, constructed from sample accession ERS474305 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_5).  This submission includes reads tagged with the sequence CCTCCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474305">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474305</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581065</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362712</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_5#4" accession="ERX1415842" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415842</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_5#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_5#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362713, constructed from sample accession ERS474316 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_5).  This submission includes reads tagged with the sequence CGAACTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474316">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474316</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581076</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362713</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_5#5" accession="ERX1415843" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415843</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_5#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_5#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362714, constructed from sample accession ERS474332 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_5).  This submission includes reads tagged with the sequence CGACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474332">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474332</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581092</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362714</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_5#6" accession="ERX1415844" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415844</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_5#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_5#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362715, constructed from sample accession ERS474340 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_5).  This submission includes reads tagged with the sequence CGCATAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474340">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474340</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581100</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362715</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_5#7" accession="ERX1415845" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415845</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_5#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_5#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362716, constructed from sample accession ERS474349 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_5).  This submission includes reads tagged with the sequence CTCAATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474349">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474349</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581109</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362716</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_5#8" accession="ERX1415846" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415846</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_5#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_5#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362717, constructed from sample accession ERS474362 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_5).  This submission includes reads tagged with the sequence CTGAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474362">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474362</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581122</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362717</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_5#9" accession="ERX1415847" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415847</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_5#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_5#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362718, constructed from sample accession ERS474371 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_5).  This submission includes reads tagged with the sequence CTGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474371">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474371</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581131</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362718</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_5#10" accession="ERX1415848" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415848</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_5#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_5#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362719, constructed from sample accession ERS474385 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_5).  This submission includes reads tagged with the sequence GAATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474385">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474385</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581145</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362719</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_5#11" accession="ERX1415849" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415849</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_5#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_5#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362720, constructed from sample accession ERS474396 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_5).  This submission includes reads tagged with the sequence CAAGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474396">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474396</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581156</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362720</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_5#12" accession="ERX1415850" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415850</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_5#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_5#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362721, constructed from sample accession ERS474418 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_5).  This submission includes reads tagged with the sequence GAGCTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474418">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474418</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581178</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362721</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_6#1" accession="ERX1415851" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415851</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_6#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_6#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362710, constructed from sample accession ERS474277 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_6).  This submission includes reads tagged with the sequence CCGAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474277">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474277</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581037</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362710</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_6#2" accession="ERX1415852" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415852</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_6#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_6#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362711, constructed from sample accession ERS474292 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_6).  This submission includes reads tagged with the sequence CCGTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474292">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474292</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581052</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362711</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_6#3" accession="ERX1415853" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415853</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_6#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_6#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362712, constructed from sample accession ERS474305 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_6).  This submission includes reads tagged with the sequence CCTCCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474305">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474305</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581065</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362712</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_6#4" accession="ERX1415854" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415854</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_6#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_6#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362713, constructed from sample accession ERS474316 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_6).  This submission includes reads tagged with the sequence CGAACTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474316">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474316</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581076</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362713</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_6#5" accession="ERX1415855" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415855</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_6#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_6#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362714, constructed from sample accession ERS474332 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_6).  This submission includes reads tagged with the sequence CGACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474332">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474332</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581092</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362714</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_6#6" accession="ERX1415856" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415856</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_6#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_6#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362715, constructed from sample accession ERS474340 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_6).  This submission includes reads tagged with the sequence CGCATAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474340">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474340</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581100</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362715</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_6#7" accession="ERX1415857" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415857</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_6#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_6#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362716, constructed from sample accession ERS474349 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_6).  This submission includes reads tagged with the sequence CTCAATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474349">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474349</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581109</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362716</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_6#8" accession="ERX1415858" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415858</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_6#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_6#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362717, constructed from sample accession ERS474362 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_6).  This submission includes reads tagged with the sequence CTGAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474362">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474362</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581122</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362717</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_6#9" accession="ERX1415859" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415859</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_6#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_6#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362718, constructed from sample accession ERS474371 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_6).  This submission includes reads tagged with the sequence CTGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474371">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474371</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581131</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362718</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_6#10" accession="ERX1415860" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415860</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_6#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_6#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362719, constructed from sample accession ERS474385 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_6).  This submission includes reads tagged with the sequence GAATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474385">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474385</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581145</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362719</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_6#11" accession="ERX1415861" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415861</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_6#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_6#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362720, constructed from sample accession ERS474396 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_6).  This submission includes reads tagged with the sequence CAAGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474396">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474396</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581156</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362720</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_6#12" accession="ERX1415862" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415862</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_6#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_6#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362721, constructed from sample accession ERS474418 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_6).  This submission includes reads tagged with the sequence GAGCTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474418">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474418</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581178</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362721</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_7#1" accession="ERX1415863" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415863</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_7#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_7#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362710, constructed from sample accession ERS474277 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_7).  This submission includes reads tagged with the sequence CCGAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474277">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474277</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581037</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362710</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_7#2" accession="ERX1415864" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415864</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_7#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_7#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362711, constructed from sample accession ERS474292 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_7).  This submission includes reads tagged with the sequence CCGTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474292">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474292</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581052</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362711</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_7#3" accession="ERX1415865" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415865</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_7#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_7#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362712, constructed from sample accession ERS474305 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_7).  This submission includes reads tagged with the sequence CCTCCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474305">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474305</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581065</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362712</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_7#4" accession="ERX1415866" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415866</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_7#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_7#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362713, constructed from sample accession ERS474316 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_7).  This submission includes reads tagged with the sequence CGAACTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474316">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474316</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581076</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362713</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_7#5" accession="ERX1415867" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415867</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_7#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_7#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362714, constructed from sample accession ERS474332 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_7).  This submission includes reads tagged with the sequence CGACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474332">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474332</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581092</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362714</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_7#6" accession="ERX1415868" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415868</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_7#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_7#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362715, constructed from sample accession ERS474340 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_7).  This submission includes reads tagged with the sequence CGCATAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474340">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474340</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581100</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362715</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_7#7" accession="ERX1415869" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415869</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_7#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_7#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362716, constructed from sample accession ERS474349 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_7).  This submission includes reads tagged with the sequence CTCAATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474349">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474349</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581109</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362716</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_7#8" accession="ERX1415870" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415870</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_7#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_7#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362717, constructed from sample accession ERS474362 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_7).  This submission includes reads tagged with the sequence CTGAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474362">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474362</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581122</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362717</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_7#9" accession="ERX1415871" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415871</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_7#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_7#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362718, constructed from sample accession ERS474371 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_7).  This submission includes reads tagged with the sequence CTGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474371">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474371</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581131</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362718</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_7#10" accession="ERX1415872" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415872</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_7#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_7#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362719, constructed from sample accession ERS474385 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_7).  This submission includes reads tagged with the sequence GAATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474385">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474385</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581145</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362719</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_7#11" accession="ERX1415873" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415873</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_7#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_7#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362720, constructed from sample accession ERS474396 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_7).  This submission includes reads tagged with the sequence CAAGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474396">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474396</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581156</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362720</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_7#12" accession="ERX1415874" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415874</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_7#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_7#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362721, constructed from sample accession ERS474418 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_7).  This submission includes reads tagged with the sequence GAGCTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474418">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474418</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581178</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362721</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_8#1" accession="ERX1415875" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415875</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_8#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_8#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362710, constructed from sample accession ERS474277 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_8).  This submission includes reads tagged with the sequence CCGAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474277">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474277</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581037</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362710</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_8#2" accession="ERX1415876" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415876</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_8#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_8#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362711, constructed from sample accession ERS474292 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_8).  This submission includes reads tagged with the sequence CCGTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474292">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474292</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581052</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362711</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_8#3" accession="ERX1415877" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415877</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_8#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_8#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362712, constructed from sample accession ERS474305 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_8).  This submission includes reads tagged with the sequence CCTCCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474305">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474305</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581065</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362712</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_8#4" accession="ERX1415878" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415878</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_8#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_8#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362713, constructed from sample accession ERS474316 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_8).  This submission includes reads tagged with the sequence CGAACTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474316">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474316</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581076</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362713</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_8#5" accession="ERX1415879" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415879</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_8#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_8#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362714, constructed from sample accession ERS474332 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_8).  This submission includes reads tagged with the sequence CGACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474332">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474332</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581092</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362714</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_8#6" accession="ERX1415880" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415880</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_8#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_8#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362715, constructed from sample accession ERS474340 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_8).  This submission includes reads tagged with the sequence CGCATAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474340">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474340</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581100</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362715</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_8#7" accession="ERX1415881" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415881</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_8#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_8#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362716, constructed from sample accession ERS474349 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_8).  This submission includes reads tagged with the sequence CTCAATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474349">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474349</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581109</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362716</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_8#8" accession="ERX1415882" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415882</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_8#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_8#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362717, constructed from sample accession ERS474362 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_8).  This submission includes reads tagged with the sequence CTGAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474362">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474362</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581122</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362717</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_8#9" accession="ERX1415883" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415883</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_8#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_8#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362718, constructed from sample accession ERS474371 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_8).  This submission includes reads tagged with the sequence CTGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474371">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474371</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581131</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362718</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_8#10" accession="ERX1415884" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415884</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_8#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_8#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362719, constructed from sample accession ERS474385 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_8).  This submission includes reads tagged with the sequence GAATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474385">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474385</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581145</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362719</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_8#11" accession="ERX1415885" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415885</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_8#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_8#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362720, constructed from sample accession ERS474396 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_8).  This submission includes reads tagged with the sequence CAAGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474396">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474396</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581156</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362720</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18652_8#12" accession="ERX1415886" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415886</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18652_8#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18652_8#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362721, constructed from sample accession ERS474418 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18652_8).  This submission includes reads tagged with the sequence GAGCTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474418">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474418</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581178</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362721</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_1#1" accession="ERX1415887" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415887</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362758, constructed from sample accession ERS474281 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_1).  This submission includes reads tagged with the sequence CCATCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474281">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474281</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581041</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362758</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_1#2" accession="ERX1415888" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415888</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362759, constructed from sample accession ERS474301 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_1).  This submission includes reads tagged with the sequence CCGACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474301">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474301</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581061</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362759</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_1#3" accession="ERX1415889" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415889</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362760, constructed from sample accession ERS474310 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_1).  This submission includes reads tagged with the sequence CCTAATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474310">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474310</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581070</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362760</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_1#4" accession="ERX1415890" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415890</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362761, constructed from sample accession ERS474325 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_1).  This submission includes reads tagged with the sequence CCTCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474325">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474325</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581085</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362761</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_1#5" accession="ERX1415891" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415891</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362762, constructed from sample accession ERS474336 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_1).  This submission includes reads tagged with the sequence CGACACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474336">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474336</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581096</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362762</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_1#6" accession="ERX1415892" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415892</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_1#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_1#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362763, constructed from sample accession ERS474344 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_1).  This submission includes reads tagged with the sequence CGGATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474344">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474344</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581104</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362763</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_1#7" accession="ERX1415893" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415893</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362764, constructed from sample accession ERS474355 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_1).  This submission includes reads tagged with the sequence CTAAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474355">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474355</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581115</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362764</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_1#8" accession="ERX1415894" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415894</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_1#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_1#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362765, constructed from sample accession ERS474367 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_1).  This submission includes reads tagged with the sequence GAACAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474367">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474367</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581127</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362765</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_1#9" accession="ERX1415895" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415895</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_1#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_1#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362766, constructed from sample accession ERS474375 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_1).  This submission includes reads tagged with the sequence GACAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474375">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474375</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581135</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362766</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_1#10" accession="ERX1415896" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415896</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_1#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_1#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362767, constructed from sample accession ERS474390 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_1).  This submission includes reads tagged with the sequence GAGTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474390">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474390</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581150</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362767</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_1#11" accession="ERX1415897" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415897</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_1#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_1#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362768, constructed from sample accession ERS474403 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_1).  This submission includes reads tagged with the sequence GATGAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474403">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474403</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581163</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362768</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_1#12" accession="ERX1415898" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415898</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_1#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_1#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362769, constructed from sample accession ERS474422 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_1).  This submission includes reads tagged with the sequence GCCAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474422">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474422</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581182</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362769</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_2#1" accession="ERX1415899" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415899</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362758, constructed from sample accession ERS474281 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_2).  This submission includes reads tagged with the sequence CCATCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474281">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474281</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581041</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362758</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_2#2" accession="ERX1415900" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415900</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362759, constructed from sample accession ERS474301 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_2).  This submission includes reads tagged with the sequence CCGACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474301">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474301</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581061</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362759</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_2#3" accession="ERX1415901" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415901</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362760, constructed from sample accession ERS474310 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_2).  This submission includes reads tagged with the sequence CCTAATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474310">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474310</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581070</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362760</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_2#4" accession="ERX1415902" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415902</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362761, constructed from sample accession ERS474325 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_2).  This submission includes reads tagged with the sequence CCTCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474325">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474325</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581085</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362761</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_2#5" accession="ERX1415903" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415903</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362762, constructed from sample accession ERS474336 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_2).  This submission includes reads tagged with the sequence CGACACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474336">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474336</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581096</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362762</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_2#6" accession="ERX1415904" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415904</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362763, constructed from sample accession ERS474344 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_2).  This submission includes reads tagged with the sequence CGGATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474344">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474344</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581104</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362763</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_2#7" accession="ERX1415905" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415905</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_2#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_2#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362764, constructed from sample accession ERS474355 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_2).  This submission includes reads tagged with the sequence CTAAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474355">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474355</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581115</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362764</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_2#8" accession="ERX1415906" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415906</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_2#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_2#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362765, constructed from sample accession ERS474367 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_2).  This submission includes reads tagged with the sequence GAACAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474367">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474367</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581127</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362765</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_2#9" accession="ERX1415907" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415907</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_2#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_2#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362766, constructed from sample accession ERS474375 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_2).  This submission includes reads tagged with the sequence GACAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474375">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474375</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581135</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362766</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_2#10" accession="ERX1415908" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415908</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_2#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_2#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362767, constructed from sample accession ERS474390 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_2).  This submission includes reads tagged with the sequence GAGTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474390">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474390</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581150</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362767</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_2#11" accession="ERX1415909" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415909</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_2#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_2#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362768, constructed from sample accession ERS474403 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_2).  This submission includes reads tagged with the sequence GATGAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474403">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474403</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581163</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362768</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_2#12" accession="ERX1415910" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415910</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_2#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_2#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362769, constructed from sample accession ERS474422 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_2).  This submission includes reads tagged with the sequence GCCAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474422">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474422</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581182</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362769</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_3#1" accession="ERX1415911" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415911</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_3#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_3#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362758, constructed from sample accession ERS474281 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_3).  This submission includes reads tagged with the sequence CCATCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474281">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474281</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581041</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362758</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_3#2" accession="ERX1415912" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415912</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_3#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_3#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362759, constructed from sample accession ERS474301 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_3).  This submission includes reads tagged with the sequence CCGACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474301">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474301</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581061</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362759</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_3#3" accession="ERX1415913" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415913</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_3#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_3#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362760, constructed from sample accession ERS474310 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_3).  This submission includes reads tagged with the sequence CCTAATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474310">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474310</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581070</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362760</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_3#4" accession="ERX1415914" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415914</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_3#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_3#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362761, constructed from sample accession ERS474325 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_3).  This submission includes reads tagged with the sequence CCTCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474325">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474325</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581085</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362761</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_3#5" accession="ERX1415915" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415915</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_3#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_3#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362762, constructed from sample accession ERS474336 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_3).  This submission includes reads tagged with the sequence CGACACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474336">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474336</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581096</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362762</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_3#6" accession="ERX1415916" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415916</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_3#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_3#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362763, constructed from sample accession ERS474344 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_3).  This submission includes reads tagged with the sequence CGGATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474344">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474344</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581104</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362763</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_3#7" accession="ERX1415917" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415917</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_3#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_3#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362764, constructed from sample accession ERS474355 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_3).  This submission includes reads tagged with the sequence CTAAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474355">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474355</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581115</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362764</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_3#8" accession="ERX1415918" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415918</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_3#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_3#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362765, constructed from sample accession ERS474367 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_3).  This submission includes reads tagged with the sequence GAACAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474367">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474367</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581127</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362765</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_3#9" accession="ERX1415919" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415919</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_3#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_3#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362766, constructed from sample accession ERS474375 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_3).  This submission includes reads tagged with the sequence GACAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474375">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474375</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581135</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362766</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_3#10" accession="ERX1415920" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415920</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_3#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_3#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362767, constructed from sample accession ERS474390 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_3).  This submission includes reads tagged with the sequence GAGTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474390">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474390</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581150</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362767</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_3#11" accession="ERX1415921" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415921</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_3#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_3#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362768, constructed from sample accession ERS474403 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_3).  This submission includes reads tagged with the sequence GATGAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474403">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474403</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581163</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362768</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_3#12" accession="ERX1415922" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415922</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_3#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_3#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362769, constructed from sample accession ERS474422 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_3).  This submission includes reads tagged with the sequence GCCAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474422">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474422</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581182</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362769</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_4#1" accession="ERX1415923" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415923</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_4#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_4#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362758, constructed from sample accession ERS474281 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_4).  This submission includes reads tagged with the sequence CCATCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474281">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474281</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581041</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362758</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_4#2" accession="ERX1415924" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415924</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_4#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_4#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362759, constructed from sample accession ERS474301 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_4).  This submission includes reads tagged with the sequence CCGACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474301">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474301</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581061</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362759</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_4#3" accession="ERX1415925" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415925</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_4#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_4#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362760, constructed from sample accession ERS474310 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_4).  This submission includes reads tagged with the sequence CCTAATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474310">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474310</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581070</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362760</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_4#4" accession="ERX1415926" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415926</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_4#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_4#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362761, constructed from sample accession ERS474325 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_4).  This submission includes reads tagged with the sequence CCTCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474325">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474325</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581085</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362761</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_4#5" accession="ERX1415927" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415927</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_4#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_4#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362762, constructed from sample accession ERS474336 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_4).  This submission includes reads tagged with the sequence CGACACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474336">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474336</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581096</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362762</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_4#6" accession="ERX1415928" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415928</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_4#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_4#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362763, constructed from sample accession ERS474344 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_4).  This submission includes reads tagged with the sequence CGGATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474344">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474344</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581104</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362763</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_4#7" accession="ERX1415929" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415929</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_4#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_4#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362764, constructed from sample accession ERS474355 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_4).  This submission includes reads tagged with the sequence CTAAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474355">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474355</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581115</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362764</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_4#8" accession="ERX1415930" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415930</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_4#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_4#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362765, constructed from sample accession ERS474367 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_4).  This submission includes reads tagged with the sequence GAACAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474367">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474367</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581127</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362765</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_4#9" accession="ERX1415931" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415931</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_4#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_4#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362766, constructed from sample accession ERS474375 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_4).  This submission includes reads tagged with the sequence GACAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474375">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474375</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581135</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362766</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_4#10" accession="ERX1415932" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415932</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_4#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_4#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362767, constructed from sample accession ERS474390 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_4).  This submission includes reads tagged with the sequence GAGTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474390">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474390</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581150</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362767</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_4#11" accession="ERX1415933" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415933</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_4#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_4#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362768, constructed from sample accession ERS474403 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_4).  This submission includes reads tagged with the sequence GATGAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474403">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474403</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581163</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362768</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_4#12" accession="ERX1415934" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415934</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_4#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_4#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362769, constructed from sample accession ERS474422 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_4).  This submission includes reads tagged with the sequence GCCAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474422">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474422</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581182</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362769</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_5#1" accession="ERX1415935" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415935</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_5#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_5#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362758, constructed from sample accession ERS474281 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_5).  This submission includes reads tagged with the sequence CCATCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474281">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474281</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581041</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362758</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_5#2" accession="ERX1415936" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415936</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_5#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_5#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362759, constructed from sample accession ERS474301 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_5).  This submission includes reads tagged with the sequence CCGACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474301">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474301</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581061</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362759</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_5#3" accession="ERX1415937" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415937</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_5#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_5#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362760, constructed from sample accession ERS474310 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_5).  This submission includes reads tagged with the sequence CCTAATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474310">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474310</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581070</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362760</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_5#4" accession="ERX1415938" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415938</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_5#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_5#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362761, constructed from sample accession ERS474325 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_5).  This submission includes reads tagged with the sequence CCTCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474325">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474325</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581085</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362761</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_5#5" accession="ERX1415939" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415939</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_5#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_5#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362762, constructed from sample accession ERS474336 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_5).  This submission includes reads tagged with the sequence CGACACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474336">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474336</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581096</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362762</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_5#6" accession="ERX1415940" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415940</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_5#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_5#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362763, constructed from sample accession ERS474344 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_5).  This submission includes reads tagged with the sequence CGGATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474344">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474344</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581104</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362763</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_5#7" accession="ERX1415941" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415941</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_5#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_5#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362764, constructed from sample accession ERS474355 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_5).  This submission includes reads tagged with the sequence CTAAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474355">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474355</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581115</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362764</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_5#8" accession="ERX1415942" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415942</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_5#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_5#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362765, constructed from sample accession ERS474367 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_5).  This submission includes reads tagged with the sequence GAACAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474367">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474367</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581127</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362765</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_5#9" accession="ERX1415943" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415943</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_5#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_5#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362766, constructed from sample accession ERS474375 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_5).  This submission includes reads tagged with the sequence GACAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474375">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474375</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581135</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362766</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_5#10" accession="ERX1415944" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415944</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_5#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_5#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362767, constructed from sample accession ERS474390 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_5).  This submission includes reads tagged with the sequence GAGTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474390">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474390</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581150</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362767</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_5#11" accession="ERX1415945" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415945</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_5#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_5#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362768, constructed from sample accession ERS474403 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_5).  This submission includes reads tagged with the sequence GATGAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474403">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474403</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581163</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362768</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_5#12" accession="ERX1415946" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415946</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_5#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_5#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362769, constructed from sample accession ERS474422 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_5).  This submission includes reads tagged with the sequence GCCAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474422">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474422</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581182</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362769</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_6#1" accession="ERX1415947" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415947</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_6#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_6#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362758, constructed from sample accession ERS474281 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_6).  This submission includes reads tagged with the sequence CCATCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474281">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474281</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581041</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362758</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_6#2" accession="ERX1415948" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415948</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_6#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_6#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362759, constructed from sample accession ERS474301 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_6).  This submission includes reads tagged with the sequence CCGACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474301">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474301</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581061</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362759</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_6#3" accession="ERX1415949" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415949</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_6#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_6#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362760, constructed from sample accession ERS474310 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_6).  This submission includes reads tagged with the sequence CCTAATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474310">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474310</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581070</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362760</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_6#4" accession="ERX1415950" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415950</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_6#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_6#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362761, constructed from sample accession ERS474325 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_6).  This submission includes reads tagged with the sequence CCTCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474325">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474325</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581085</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362761</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_6#5" accession="ERX1415951" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415951</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_6#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_6#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362762, constructed from sample accession ERS474336 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_6).  This submission includes reads tagged with the sequence CGACACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474336">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474336</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581096</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362762</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_6#6" accession="ERX1415952" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415952</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_6#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_6#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362763, constructed from sample accession ERS474344 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_6).  This submission includes reads tagged with the sequence CGGATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474344">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474344</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581104</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362763</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_6#7" accession="ERX1415953" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415953</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_6#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_6#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362764, constructed from sample accession ERS474355 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_6).  This submission includes reads tagged with the sequence CTAAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474355">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474355</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581115</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362764</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_6#8" accession="ERX1415954" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415954</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_6#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_6#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362765, constructed from sample accession ERS474367 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_6).  This submission includes reads tagged with the sequence GAACAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474367">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474367</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581127</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362765</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_6#9" accession="ERX1415955" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415955</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_6#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_6#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362766, constructed from sample accession ERS474375 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_6).  This submission includes reads tagged with the sequence GACAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474375">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474375</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581135</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362766</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_6#10" accession="ERX1415956" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415956</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_6#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_6#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362767, constructed from sample accession ERS474390 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_6).  This submission includes reads tagged with the sequence GAGTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474390">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474390</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581150</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362767</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_6#11" accession="ERX1415957" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415957</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_6#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_6#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362768, constructed from sample accession ERS474403 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_6).  This submission includes reads tagged with the sequence GATGAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474403">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474403</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581163</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362768</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_6#12" accession="ERX1415958" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415958</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_6#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_6#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362769, constructed from sample accession ERS474422 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_6).  This submission includes reads tagged with the sequence GCCAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474422">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474422</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581182</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362769</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_7#1" accession="ERX1415959" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415959</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_7#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_7#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362758, constructed from sample accession ERS474281 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_7).  This submission includes reads tagged with the sequence CCATCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474281">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474281</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581041</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362758</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_7#2" accession="ERX1415960" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415960</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_7#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_7#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362759, constructed from sample accession ERS474301 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_7).  This submission includes reads tagged with the sequence CCGACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474301">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474301</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581061</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362759</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_7#3" accession="ERX1415961" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415961</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_7#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_7#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362760, constructed from sample accession ERS474310 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_7).  This submission includes reads tagged with the sequence CCTAATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474310">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474310</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581070</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362760</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_7#4" accession="ERX1415962" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415962</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_7#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_7#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362761, constructed from sample accession ERS474325 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_7).  This submission includes reads tagged with the sequence CCTCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474325">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474325</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581085</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362761</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_7#5" accession="ERX1415963" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415963</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_7#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_7#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362762, constructed from sample accession ERS474336 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_7).  This submission includes reads tagged with the sequence CGACACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474336">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474336</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581096</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362762</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_7#6" accession="ERX1415964" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415964</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_7#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_7#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362763, constructed from sample accession ERS474344 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_7).  This submission includes reads tagged with the sequence CGGATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474344">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474344</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581104</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362763</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_7#7" accession="ERX1415965" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415965</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_7#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_7#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362764, constructed from sample accession ERS474355 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_7).  This submission includes reads tagged with the sequence CTAAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474355">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474355</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581115</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362764</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_7#8" accession="ERX1415966" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415966</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_7#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_7#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362765, constructed from sample accession ERS474367 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_7).  This submission includes reads tagged with the sequence GAACAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474367">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474367</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581127</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362765</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_7#9" accession="ERX1415967" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415967</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_7#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_7#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362766, constructed from sample accession ERS474375 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_7).  This submission includes reads tagged with the sequence GACAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474375">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474375</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581135</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362766</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_7#10" accession="ERX1415968" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415968</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_7#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_7#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362767, constructed from sample accession ERS474390 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_7).  This submission includes reads tagged with the sequence GAGTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474390">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474390</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581150</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362767</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_7#11" accession="ERX1415969" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415969</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_7#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_7#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362768, constructed from sample accession ERS474403 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_7).  This submission includes reads tagged with the sequence GATGAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474403">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474403</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581163</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362768</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_7#12" accession="ERX1415970" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415970</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_7#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_7#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362769, constructed from sample accession ERS474422 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_7).  This submission includes reads tagged with the sequence GCCAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474422">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474422</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581182</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362769</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_8#1" accession="ERX1415971" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415971</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_8#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_8#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362758, constructed from sample accession ERS474281 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_8).  This submission includes reads tagged with the sequence CCATCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474281">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474281</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581041</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362758</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_8#2" accession="ERX1415972" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415972</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_8#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_8#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362759, constructed from sample accession ERS474301 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_8).  This submission includes reads tagged with the sequence CCGACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474301">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474301</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581061</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362759</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_8#3" accession="ERX1415973" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415973</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_8#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_8#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362760, constructed from sample accession ERS474310 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_8).  This submission includes reads tagged with the sequence CCTAATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474310">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474310</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581070</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362760</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_8#4" accession="ERX1415974" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415974</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_8#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_8#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362761, constructed from sample accession ERS474325 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_8).  This submission includes reads tagged with the sequence CCTCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474325">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474325</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581085</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362761</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_8#5" accession="ERX1415975" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415975</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_8#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_8#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362762, constructed from sample accession ERS474336 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_8).  This submission includes reads tagged with the sequence CGACACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474336">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474336</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581096</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362762</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_8#6" accession="ERX1415976" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415976</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_8#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_8#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362763, constructed from sample accession ERS474344 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_8).  This submission includes reads tagged with the sequence CGGATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474344">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474344</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581104</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362763</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_8#7" accession="ERX1415977" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415977</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_8#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_8#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362764, constructed from sample accession ERS474355 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_8).  This submission includes reads tagged with the sequence CTAAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474355">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474355</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581115</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362764</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_8#8" accession="ERX1415978" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415978</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_8#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_8#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362765, constructed from sample accession ERS474367 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_8).  This submission includes reads tagged with the sequence GAACAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474367">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474367</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581127</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362765</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_8#9" accession="ERX1415979" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415979</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_8#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_8#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362766, constructed from sample accession ERS474375 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_8).  This submission includes reads tagged with the sequence GACAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474375">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474375</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581135</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362766</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_8#10" accession="ERX1415980" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415980</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_8#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_8#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362767, constructed from sample accession ERS474390 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_8).  This submission includes reads tagged with the sequence GAGTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474390">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474390</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581150</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362767</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_8#11" accession="ERX1415981" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415981</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_8#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_8#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362768, constructed from sample accession ERS474403 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_8).  This submission includes reads tagged with the sequence GATGAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474403">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474403</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581163</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362768</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18654_8#12" accession="ERX1415982" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415982</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18654_8#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18654_8#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362769, constructed from sample accession ERS474422 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18654_8).  This submission includes reads tagged with the sequence GCCAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474422">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474422</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581182</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362769</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_1#1" accession="ERX1415983" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415983</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362722, constructed from sample accession ERS474278 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_1).  This submission includes reads tagged with the sequence GATAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474278">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474278</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581038</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362722</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_1#2" accession="ERX1415984" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415984</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362723, constructed from sample accession ERS474293 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_1).  This submission includes reads tagged with the sequence GCCACAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474293">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474293</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581053</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362723</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_1#3" accession="ERX1415985" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415985</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362724, constructed from sample accession ERS474307 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_1).  This submission includes reads tagged with the sequence GCGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474307">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474307</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581067</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362724</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_1#4" accession="ERX1415986" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415986</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362725, constructed from sample accession ERS474320 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_1).  This submission includes reads tagged with the sequence GCTAACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474320">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474320</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581080</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362725</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_1#5" accession="ERX1415987" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415987</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362726, constructed from sample accession ERS474333 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_1).  This submission includes reads tagged with the sequence GCTCGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474333">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474333</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581093</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362726</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_1#6" accession="ERX1415988" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415988</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_1#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_1#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362727, constructed from sample accession ERS474341 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_1).  This submission includes reads tagged with the sequence GGAGAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474341">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474341</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581101</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362727</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_1#7" accession="ERX1415989" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415989</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362728, constructed from sample accession ERS474351 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_1).  This submission includes reads tagged with the sequence GGTGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474351">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581111</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362728</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_1#8" accession="ERX1415990" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415990</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_1#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_1#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362729, constructed from sample accession ERS474363 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_1).  This submission includes reads tagged with the sequence GTACGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474363">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474363</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581123</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362729</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_1#9" accession="ERX1415991" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415991</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_1#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_1#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362730, constructed from sample accession ERS474372 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_1).  This submission includes reads tagged with the sequence GTCGTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474372">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474372</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581132</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362730</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_1#10" accession="ERX1415992" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415992</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_1#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_1#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362731, constructed from sample accession ERS474386 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_1).  This submission includes reads tagged with the sequence GTCTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474386">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474386</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581146</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362731</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_1#11" accession="ERX1415993" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415993</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_1#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_1#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362732, constructed from sample accession ERS474397 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_1).  This submission includes reads tagged with the sequence GTGTTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474397">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474397</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581157</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362732</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_1#12" accession="ERX1415994" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415994</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_1#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_1#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362733, constructed from sample accession ERS474419 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_1).  This submission includes reads tagged with the sequence TAGGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474419">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474419</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581179</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362733</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_2#1" accession="ERX1415995" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415995</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362722, constructed from sample accession ERS474278 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_2).  This submission includes reads tagged with the sequence GATAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474278">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474278</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581038</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362722</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_2#2" accession="ERX1415996" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415996</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362723, constructed from sample accession ERS474293 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_2).  This submission includes reads tagged with the sequence GCCACAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474293">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474293</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581053</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362723</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_2#3" accession="ERX1415997" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415997</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362724, constructed from sample accession ERS474307 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_2).  This submission includes reads tagged with the sequence GCGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474307">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474307</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581067</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362724</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_2#4" accession="ERX1415998" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415998</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362725, constructed from sample accession ERS474320 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_2).  This submission includes reads tagged with the sequence GCTAACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474320">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474320</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581080</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362725</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_2#5" accession="ERX1415999" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1415999</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362726, constructed from sample accession ERS474333 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_2).  This submission includes reads tagged with the sequence GCTCGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474333">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474333</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581093</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362726</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_2#6" accession="ERX1416000" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416000</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362727, constructed from sample accession ERS474341 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_2).  This submission includes reads tagged with the sequence GGAGAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474341">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474341</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581101</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362727</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_2#7" accession="ERX1416001" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416001</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_2#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_2#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362728, constructed from sample accession ERS474351 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_2).  This submission includes reads tagged with the sequence GGTGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474351">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581111</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362728</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_2#8" accession="ERX1416002" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416002</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_2#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_2#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362729, constructed from sample accession ERS474363 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_2).  This submission includes reads tagged with the sequence GTACGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474363">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474363</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581123</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362729</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_2#9" accession="ERX1416003" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416003</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_2#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_2#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362730, constructed from sample accession ERS474372 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_2).  This submission includes reads tagged with the sequence GTCGTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474372">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474372</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581132</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362730</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_2#10" accession="ERX1416004" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416004</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_2#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_2#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362731, constructed from sample accession ERS474386 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_2).  This submission includes reads tagged with the sequence GTCTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474386">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474386</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581146</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362731</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_2#11" accession="ERX1416005" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416005</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_2#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_2#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362732, constructed from sample accession ERS474397 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_2).  This submission includes reads tagged with the sequence GTGTTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474397">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474397</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581157</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362732</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_2#12" accession="ERX1416006" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416006</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_2#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_2#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362733, constructed from sample accession ERS474419 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_2).  This submission includes reads tagged with the sequence TAGGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474419">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474419</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581179</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362733</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="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_3#1" accession="ERX1416007" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416007</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_3#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_3#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362722, constructed from sample accession ERS474278 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_3).  This submission includes reads tagged with the sequence GATAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474278">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474278</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581038</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362722</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_3#2" accession="ERX1416008" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416008</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_3#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_3#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362723, constructed from sample accession ERS474293 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_3).  This submission includes reads tagged with the sequence GCCACAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474293">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474293</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581053</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362723</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_3#3" accession="ERX1416009" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416009</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_3#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_3#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362724, constructed from sample accession ERS474307 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_3).  This submission includes reads tagged with the sequence GCGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474307">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474307</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581067</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362724</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_3#4" accession="ERX1416010" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416010</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_3#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_3#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362725, constructed from sample accession ERS474320 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_3).  This submission includes reads tagged with the sequence GCTAACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474320">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474320</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581080</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362725</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_3#5" accession="ERX1416011" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416011</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_3#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_3#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362726, constructed from sample accession ERS474333 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_3).  This submission includes reads tagged with the sequence GCTCGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474333">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474333</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581093</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362726</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_3#6" accession="ERX1416012" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416012</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_3#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_3#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362727, constructed from sample accession ERS474341 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_3).  This submission includes reads tagged with the sequence GGAGAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474341">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474341</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581101</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362727</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_3#7" accession="ERX1416013" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416013</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_3#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_3#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362728, constructed from sample accession ERS474351 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_3).  This submission includes reads tagged with the sequence GGTGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474351">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581111</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362728</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_3#8" accession="ERX1416014" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416014</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_3#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_3#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362729, constructed from sample accession ERS474363 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_3).  This submission includes reads tagged with the sequence GTACGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474363">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474363</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581123</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362729</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_3#9" accession="ERX1416015" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416015</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_3#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_3#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362730, constructed from sample accession ERS474372 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_3).  This submission includes reads tagged with the sequence GTCGTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474372">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474372</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581132</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362730</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_3#10" accession="ERX1416016" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416016</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_3#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_3#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362731, constructed from sample accession ERS474386 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_3).  This submission includes reads tagged with the sequence GTCTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474386">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474386</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581146</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362731</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_3#11" accession="ERX1416017" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416017</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_3#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_3#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362732, constructed from sample accession ERS474397 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_3).  This submission includes reads tagged with the sequence GTGTTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474397">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474397</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581157</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362732</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_3#12" accession="ERX1416018" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416018</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_3#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_3#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362733, constructed from sample accession ERS474419 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_3).  This submission includes reads tagged with the sequence TAGGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474419">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474419</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581179</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362733</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_4#1" accession="ERX1416019" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416019</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_4#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_4#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362722, constructed from sample accession ERS474278 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_4).  This submission includes reads tagged with the sequence GATAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474278">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474278</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581038</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362722</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_4#2" accession="ERX1416020" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416020</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_4#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_4#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362723, constructed from sample accession ERS474293 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_4).  This submission includes reads tagged with the sequence GCCACAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474293">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474293</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581053</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362723</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_4#3" accession="ERX1416021" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416021</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_4#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_4#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362724, constructed from sample accession ERS474307 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_4).  This submission includes reads tagged with the sequence GCGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474307">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474307</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581067</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362724</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_4#4" accession="ERX1416022" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416022</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_4#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_4#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362725, constructed from sample accession ERS474320 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_4).  This submission includes reads tagged with the sequence GCTAACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474320">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474320</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581080</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362725</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_4#5" accession="ERX1416023" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416023</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_4#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_4#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362726, constructed from sample accession ERS474333 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_4).  This submission includes reads tagged with the sequence GCTCGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474333">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474333</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581093</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362726</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_4#6" accession="ERX1416024" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416024</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_4#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_4#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362727, constructed from sample accession ERS474341 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_4).  This submission includes reads tagged with the sequence GGAGAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474341">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474341</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581101</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362727</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_4#7" accession="ERX1416025" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416025</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_4#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_4#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362728, constructed from sample accession ERS474351 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_4).  This submission includes reads tagged with the sequence GGTGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474351">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581111</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362728</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_4#8" accession="ERX1416026" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416026</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_4#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_4#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362729, constructed from sample accession ERS474363 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_4).  This submission includes reads tagged with the sequence GTACGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474363">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474363</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581123</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362729</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_4#9" accession="ERX1416027" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416027</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_4#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_4#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362730, constructed from sample accession ERS474372 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_4).  This submission includes reads tagged with the sequence GTCGTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474372">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474372</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581132</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362730</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_4#10" accession="ERX1416028" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416028</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_4#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_4#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362731, constructed from sample accession ERS474386 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_4).  This submission includes reads tagged with the sequence GTCTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474386">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474386</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581146</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362731</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_4#11" accession="ERX1416029" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416029</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_4#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_4#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362732, constructed from sample accession ERS474397 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_4).  This submission includes reads tagged with the sequence GTGTTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474397">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474397</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581157</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362732</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_4#12" accession="ERX1416030" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416030</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_4#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_4#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362733, constructed from sample accession ERS474419 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_4).  This submission includes reads tagged with the sequence TAGGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474419">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474419</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581179</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362733</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_5#1" accession="ERX1416031" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416031</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_5#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_5#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362722, constructed from sample accession ERS474278 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_5).  This submission includes reads tagged with the sequence GATAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474278">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474278</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581038</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362722</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_5#2" accession="ERX1416032" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416032</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_5#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_5#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362723, constructed from sample accession ERS474293 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_5).  This submission includes reads tagged with the sequence GCCACAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474293">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474293</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581053</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362723</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_5#3" accession="ERX1416033" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416033</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_5#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_5#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362724, constructed from sample accession ERS474307 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_5).  This submission includes reads tagged with the sequence GCGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474307">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474307</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581067</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362724</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_5#4" accession="ERX1416034" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416034</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_5#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_5#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362725, constructed from sample accession ERS474320 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_5).  This submission includes reads tagged with the sequence GCTAACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474320">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474320</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581080</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362725</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_5#5" accession="ERX1416035" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416035</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_5#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_5#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362726, constructed from sample accession ERS474333 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_5).  This submission includes reads tagged with the sequence GCTCGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474333">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474333</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581093</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362726</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_5#6" accession="ERX1416036" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416036</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_5#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_5#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362727, constructed from sample accession ERS474341 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_5).  This submission includes reads tagged with the sequence GGAGAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474341">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474341</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581101</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362727</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_5#7" accession="ERX1416037" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416037</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_5#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_5#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362728, constructed from sample accession ERS474351 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_5).  This submission includes reads tagged with the sequence GGTGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474351">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581111</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362728</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_5#8" accession="ERX1416038" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416038</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_5#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_5#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362729, constructed from sample accession ERS474363 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_5).  This submission includes reads tagged with the sequence GTACGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474363">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474363</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581123</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362729</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_5#9" accession="ERX1416039" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416039</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_5#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_5#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362730, constructed from sample accession ERS474372 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_5).  This submission includes reads tagged with the sequence GTCGTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474372">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474372</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581132</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362730</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_5#10" accession="ERX1416040" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416040</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_5#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_5#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362731, constructed from sample accession ERS474386 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_5).  This submission includes reads tagged with the sequence GTCTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474386">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474386</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581146</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362731</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_5#11" accession="ERX1416041" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416041</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_5#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_5#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362732, constructed from sample accession ERS474397 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_5).  This submission includes reads tagged with the sequence GTGTTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474397">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474397</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581157</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362732</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_5#12" accession="ERX1416042" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416042</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_5#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_5#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362733, constructed from sample accession ERS474419 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_5).  This submission includes reads tagged with the sequence TAGGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474419">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474419</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581179</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362733</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_6#1" accession="ERX1416043" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416043</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_6#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_6#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362722, constructed from sample accession ERS474278 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_6).  This submission includes reads tagged with the sequence GATAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474278">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474278</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581038</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362722</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_6#2" accession="ERX1416044" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416044</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_6#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_6#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362723, constructed from sample accession ERS474293 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_6).  This submission includes reads tagged with the sequence GCCACAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474293">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474293</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581053</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362723</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_6#3" accession="ERX1416045" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416045</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_6#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_6#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362724, constructed from sample accession ERS474307 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_6).  This submission includes reads tagged with the sequence GCGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474307">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474307</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581067</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362724</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_6#4" accession="ERX1416046" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416046</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_6#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_6#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362725, constructed from sample accession ERS474320 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_6).  This submission includes reads tagged with the sequence GCTAACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474320">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474320</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581080</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362725</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_6#5" accession="ERX1416047" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416047</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_6#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_6#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362726, constructed from sample accession ERS474333 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_6).  This submission includes reads tagged with the sequence GCTCGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474333">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474333</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581093</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362726</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_6#6" accession="ERX1416048" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416048</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_6#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_6#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362727, constructed from sample accession ERS474341 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_6).  This submission includes reads tagged with the sequence GGAGAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474341">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474341</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581101</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362727</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_6#7" accession="ERX1416049" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416049</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_6#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_6#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362728, constructed from sample accession ERS474351 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_6).  This submission includes reads tagged with the sequence GGTGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474351">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581111</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362728</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_6#8" accession="ERX1416050" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416050</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_6#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_6#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362729, constructed from sample accession ERS474363 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_6).  This submission includes reads tagged with the sequence GTACGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474363">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474363</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581123</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362729</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_6#9" accession="ERX1416051" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416051</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_6#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_6#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362730, constructed from sample accession ERS474372 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_6).  This submission includes reads tagged with the sequence GTCGTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474372">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474372</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581132</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362730</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_6#10" accession="ERX1416052" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416052</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_6#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_6#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362731, constructed from sample accession ERS474386 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_6).  This submission includes reads tagged with the sequence GTCTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474386">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474386</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581146</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362731</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_6#11" accession="ERX1416053" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416053</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_6#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_6#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362732, constructed from sample accession ERS474397 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_6).  This submission includes reads tagged with the sequence GTGTTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474397">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474397</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581157</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362732</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_6#12" accession="ERX1416054" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416054</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_6#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_6#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362733, constructed from sample accession ERS474419 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_6).  This submission includes reads tagged with the sequence TAGGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474419">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474419</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581179</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362733</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_7#1" accession="ERX1416055" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416055</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_7#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_7#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362722, constructed from sample accession ERS474278 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_7).  This submission includes reads tagged with the sequence GATAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474278">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474278</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581038</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362722</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_7#2" accession="ERX1416056" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416056</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_7#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_7#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362723, constructed from sample accession ERS474293 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_7).  This submission includes reads tagged with the sequence GCCACAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474293">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474293</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581053</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362723</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_7#3" accession="ERX1416057" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416057</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_7#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_7#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362724, constructed from sample accession ERS474307 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_7).  This submission includes reads tagged with the sequence GCGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474307">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474307</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581067</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362724</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_7#4" accession="ERX1416058" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416058</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_7#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_7#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362725, constructed from sample accession ERS474320 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_7).  This submission includes reads tagged with the sequence GCTAACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474320">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474320</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581080</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362725</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_7#5" accession="ERX1416059" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416059</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_7#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_7#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362726, constructed from sample accession ERS474333 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_7).  This submission includes reads tagged with the sequence GCTCGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474333">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474333</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581093</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362726</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_7#6" accession="ERX1416060" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416060</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_7#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_7#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362727, constructed from sample accession ERS474341 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_7).  This submission includes reads tagged with the sequence GGAGAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474341">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474341</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581101</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362727</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_7#7" accession="ERX1416061" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416061</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_7#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_7#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362728, constructed from sample accession ERS474351 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_7).  This submission includes reads tagged with the sequence GGTGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474351">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581111</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362728</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_7#8" accession="ERX1416062" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416062</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_7#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_7#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362729, constructed from sample accession ERS474363 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_7).  This submission includes reads tagged with the sequence GTACGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474363">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474363</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581123</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362729</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_7#9" accession="ERX1416063" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416063</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_7#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_7#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362730, constructed from sample accession ERS474372 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_7).  This submission includes reads tagged with the sequence GTCGTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474372">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474372</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581132</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362730</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_7#10" accession="ERX1416064" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416064</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_7#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_7#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362731, constructed from sample accession ERS474386 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_7).  This submission includes reads tagged with the sequence GTCTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474386">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474386</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581146</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362731</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_7#11" accession="ERX1416065" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416065</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_7#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_7#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362732, constructed from sample accession ERS474397 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_7).  This submission includes reads tagged with the sequence GTGTTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474397">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474397</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581157</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362732</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_7#12" accession="ERX1416066" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416066</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_7#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_7#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362733, constructed from sample accession ERS474419 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_7).  This submission includes reads tagged with the sequence TAGGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474419">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474419</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581179</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362733</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_8#1" accession="ERX1416067" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416067</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_8#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_8#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362722, constructed from sample accession ERS474278 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_8).  This submission includes reads tagged with the sequence GATAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474278">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474278</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581038</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362722</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="465" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_8#2" accession="ERX1416068" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416068</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_8#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_8#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362723, constructed from sample accession ERS474293 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_8).  This submission includes reads tagged with the sequence GCCACAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474293">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474293</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581053</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362723</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="465" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_8#3" accession="ERX1416069" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416069</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_8#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_8#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362724, constructed from sample accession ERS474307 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_8).  This submission includes reads tagged with the sequence GCGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474307">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474307</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581067</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362724</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="465" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_8#4" accession="ERX1416070" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416070</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_8#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_8#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362725, constructed from sample accession ERS474320 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_8).  This submission includes reads tagged with the sequence GCTAACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474320">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474320</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581080</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362725</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="465" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_8#5" accession="ERX1416071" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416071</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_8#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_8#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362726, constructed from sample accession ERS474333 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_8).  This submission includes reads tagged with the sequence GCTCGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474333">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474333</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581093</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362726</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="465" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_8#6" accession="ERX1416072" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416072</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_8#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_8#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362727, constructed from sample accession ERS474341 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_8).  This submission includes reads tagged with the sequence GGAGAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474341">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474341</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581101</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362727</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="465" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_8#7" accession="ERX1416073" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416073</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_8#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_8#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362728, constructed from sample accession ERS474351 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_8).  This submission includes reads tagged with the sequence GGTGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474351">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581111</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362728</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="465" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_8#8" accession="ERX1416074" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416074</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_8#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_8#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362729, constructed from sample accession ERS474363 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_8).  This submission includes reads tagged with the sequence GTACGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474363">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474363</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581123</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362729</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="465" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_8#9" accession="ERX1416075" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416075</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_8#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_8#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362730, constructed from sample accession ERS474372 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_8).  This submission includes reads tagged with the sequence GTCGTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474372">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474372</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581132</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362730</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="465" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_8#10" accession="ERX1416076" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416076</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_8#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_8#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362731, constructed from sample accession ERS474386 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_8).  This submission includes reads tagged with the sequence GTCTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474386">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474386</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581146</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362731</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="465" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_8#11" accession="ERX1416077" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416077</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_8#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_8#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362732, constructed from sample accession ERS474397 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_8).  This submission includes reads tagged with the sequence GTGTTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474397">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474397</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581157</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362732</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="465" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18661_8#12" accession="ERX1416078" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416078</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18661_8#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18661_8#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362733, constructed from sample accession ERS474419 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18661_8).  This submission includes reads tagged with the sequence TAGGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474419">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474419</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581179</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362733</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="465" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_1#1" accession="ERX1416079" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416079</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362746, constructed from sample accession ERS474280 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_1).  This submission includes reads tagged with the sequence AATGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474280">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474280</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581040</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362746</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_1#2" accession="ERX1416080" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416080</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362747, constructed from sample accession ERS474295 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_1).  This submission includes reads tagged with the sequence ACACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474295">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474295</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581055</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362747</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_1#3" accession="ERX1416081" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416081</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362748, constructed from sample accession ERS474309 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_1).  This submission includes reads tagged with the sequence ACAGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474309">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474309</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581069</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362748</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_1#4" accession="ERX1416082" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416082</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362749, constructed from sample accession ERS474324 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_1).  This submission includes reads tagged with the sequence AGATGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474324">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474324</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581084</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362749</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_1#5" accession="ERX1416083" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416083</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362750, constructed from sample accession ERS474335 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_1).  This submission includes reads tagged with the sequence AGCACCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474335">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474335</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581095</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362750</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_1#6" accession="ERX1416084" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416084</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_1#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_1#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362751, constructed from sample accession ERS474343 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_1).  This submission includes reads tagged with the sequence AGCCATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474343">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474343</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581103</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362751</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_1#7" accession="ERX1416085" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416085</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362752, constructed from sample accession ERS474353 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_1).  This submission includes reads tagged with the sequence AGGCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474353">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474353</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581113</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362752</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_1#8" accession="ERX1416086" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416086</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_1#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_1#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362753, constructed from sample accession ERS474366 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_1).  This submission includes reads tagged with the sequence ATAGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474366">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474366</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581126</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362753</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_1#9" accession="ERX1416087" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416087</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_1#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_1#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362754, constructed from sample accession ERS474374 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_1).  This submission includes reads tagged with the sequence ATCATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474374">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474374</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581134</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362754</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_1#10" accession="ERX1416088" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416088</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_1#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_1#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362755, constructed from sample accession ERS474389 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_1).  This submission includes reads tagged with the sequence ATTGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474389">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474389</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581149</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362755</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_1#11" accession="ERX1416089" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416089</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_1#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_1#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362756, constructed from sample accession ERS474400 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_1).  This submission includes reads tagged with the sequence CAAGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474400">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474400</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581160</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362756</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_1#12" accession="ERX1416090" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416090</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_1#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_1#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362757, constructed from sample accession ERS474421 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_1).  This submission includes reads tagged with the sequence CACCTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474421">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474421</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581181</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362757</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_2#1" accession="ERX1416091" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416091</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362746, constructed from sample accession ERS474280 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_2).  This submission includes reads tagged with the sequence AATGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474280">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474280</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581040</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362746</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_2#2" accession="ERX1416092" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416092</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362747, constructed from sample accession ERS474295 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_2).  This submission includes reads tagged with the sequence ACACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474295">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474295</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581055</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362747</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_2#3" accession="ERX1416093" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416093</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362748, constructed from sample accession ERS474309 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_2).  This submission includes reads tagged with the sequence ACAGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474309">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474309</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581069</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362748</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_2#4" accession="ERX1416094" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416094</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362749, constructed from sample accession ERS474324 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_2).  This submission includes reads tagged with the sequence AGATGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474324">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474324</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581084</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362749</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_2#5" accession="ERX1416095" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416095</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362750, constructed from sample accession ERS474335 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_2).  This submission includes reads tagged with the sequence AGCACCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474335">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474335</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581095</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362750</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_2#6" accession="ERX1416096" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416096</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362751, constructed from sample accession ERS474343 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_2).  This submission includes reads tagged with the sequence AGCCATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474343">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474343</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581103</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362751</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_2#7" accession="ERX1416097" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416097</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_2#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_2#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362752, constructed from sample accession ERS474353 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_2).  This submission includes reads tagged with the sequence AGGCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474353">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474353</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581113</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362752</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_2#8" accession="ERX1416098" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416098</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_2#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_2#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362753, constructed from sample accession ERS474366 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_2).  This submission includes reads tagged with the sequence ATAGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474366">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474366</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581126</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362753</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_2#9" accession="ERX1416099" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416099</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_2#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_2#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362754, constructed from sample accession ERS474374 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_2).  This submission includes reads tagged with the sequence ATCATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474374">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474374</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581134</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362754</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_2#10" accession="ERX1416100" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416100</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_2#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_2#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362755, constructed from sample accession ERS474389 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_2).  This submission includes reads tagged with the sequence ATTGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474389">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474389</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581149</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362755</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_2#11" accession="ERX1416101" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416101</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_2#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_2#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362756, constructed from sample accession ERS474400 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_2).  This submission includes reads tagged with the sequence CAAGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474400">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474400</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581160</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362756</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_2#12" accession="ERX1416102" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416102</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_2#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_2#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362757, constructed from sample accession ERS474421 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_2).  This submission includes reads tagged with the sequence CACCTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474421">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474421</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581181</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362757</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" 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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_3#1" accession="ERX1416103" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416103</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_3#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_3#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362746, constructed from sample accession ERS474280 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_3).  This submission includes reads tagged with the sequence AATGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474280">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474280</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581040</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362746</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_3#2" accession="ERX1416104" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416104</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_3#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_3#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362747, constructed from sample accession ERS474295 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_3).  This submission includes reads tagged with the sequence ACACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474295">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474295</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581055</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362747</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_3#3" accession="ERX1416105" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416105</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_3#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_3#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362748, constructed from sample accession ERS474309 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_3).  This submission includes reads tagged with the sequence ACAGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474309">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474309</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581069</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362748</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_3#4" accession="ERX1416106" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416106</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_3#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_3#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362749, constructed from sample accession ERS474324 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_3).  This submission includes reads tagged with the sequence AGATGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474324">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474324</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581084</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362749</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_3#5" accession="ERX1416107" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416107</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_3#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_3#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362750, constructed from sample accession ERS474335 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_3).  This submission includes reads tagged with the sequence AGCACCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474335">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474335</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581095</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362750</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_3#6" accession="ERX1416108" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416108</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_3#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_3#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362751, constructed from sample accession ERS474343 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_3).  This submission includes reads tagged with the sequence AGCCATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474343">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474343</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581103</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362751</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_3#7" accession="ERX1416109" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416109</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_3#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_3#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362752, constructed from sample accession ERS474353 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_3).  This submission includes reads tagged with the sequence AGGCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474353">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474353</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581113</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362752</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_3#8" accession="ERX1416110" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416110</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_3#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_3#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362753, constructed from sample accession ERS474366 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_3).  This submission includes reads tagged with the sequence ATAGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474366">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474366</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581126</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362753</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_3#9" accession="ERX1416111" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416111</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_3#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_3#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362754, constructed from sample accession ERS474374 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_3).  This submission includes reads tagged with the sequence ATCATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474374">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474374</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581134</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362754</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_3#10" accession="ERX1416112" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416112</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_3#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_3#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362755, constructed from sample accession ERS474389 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_3).  This submission includes reads tagged with the sequence ATTGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474389">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474389</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581149</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362755</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_3#11" accession="ERX1416113" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416113</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_3#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_3#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362756, constructed from sample accession ERS474400 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_3).  This submission includes reads tagged with the sequence CAAGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474400">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474400</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581160</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362756</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_3#12" accession="ERX1416114" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416114</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_3#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_3#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362757, constructed from sample accession ERS474421 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_3).  This submission includes reads tagged with the sequence CACCTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474421">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474421</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581181</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362757</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_4#1" accession="ERX1416115" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416115</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_4#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_4#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362746, constructed from sample accession ERS474280 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_4).  This submission includes reads tagged with the sequence AATGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474280">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474280</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581040</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362746</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="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_4#2" accession="ERX1416116" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416116</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_4#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_4#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362747, constructed from sample accession ERS474295 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_4).  This submission includes reads tagged with the sequence ACACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474295">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474295</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581055</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362747</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="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_4#3" accession="ERX1416117" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416117</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_4#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_4#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362748, constructed from sample accession ERS474309 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_4).  This submission includes reads tagged with the sequence ACAGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474309">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474309</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581069</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362748</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="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_4#4" accession="ERX1416118" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416118</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_4#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_4#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362749, constructed from sample accession ERS474324 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_4).  This submission includes reads tagged with the sequence AGATGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474324">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474324</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581084</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362749</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="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_4#5" accession="ERX1416119" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416119</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_4#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_4#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362750, constructed from sample accession ERS474335 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_4).  This submission includes reads tagged with the sequence AGCACCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474335">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474335</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581095</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362750</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="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_4#6" accession="ERX1416120" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416120</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_4#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_4#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362751, constructed from sample accession ERS474343 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_4).  This submission includes reads tagged with the sequence AGCCATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474343">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474343</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581103</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362751</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="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_4#7" accession="ERX1416121" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416121</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_4#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_4#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362752, constructed from sample accession ERS474353 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_4).  This submission includes reads tagged with the sequence AGGCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474353">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474353</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581113</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362752</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="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_4#8" accession="ERX1416122" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416122</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_4#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_4#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362753, constructed from sample accession ERS474366 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_4).  This submission includes reads tagged with the sequence ATAGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474366">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474366</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581126</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362753</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="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_4#9" accession="ERX1416123" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416123</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_4#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_4#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362754, constructed from sample accession ERS474374 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_4).  This submission includes reads tagged with the sequence ATCATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474374">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474374</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581134</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362754</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="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_4#10" accession="ERX1416124" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416124</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_4#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_4#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362755, constructed from sample accession ERS474389 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_4).  This submission includes reads tagged with the sequence ATTGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474389">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474389</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581149</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362755</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="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_4#11" accession="ERX1416125" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416125</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_4#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_4#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362756, constructed from sample accession ERS474400 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_4).  This submission includes reads tagged with the sequence CAAGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474400">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474400</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581160</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362756</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="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_4#12" accession="ERX1416126" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416126</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_4#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_4#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362757, constructed from sample accession ERS474421 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_4).  This submission includes reads tagged with the sequence CACCTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474421">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474421</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581181</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362757</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="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_5#1" accession="ERX1416127" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416127</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_5#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_5#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362746, constructed from sample accession ERS474280 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_5).  This submission includes reads tagged with the sequence AATGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474280">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474280</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581040</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362746</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_5#2" accession="ERX1416128" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416128</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_5#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_5#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362747, constructed from sample accession ERS474295 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_5).  This submission includes reads tagged with the sequence ACACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474295">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474295</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581055</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362747</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_5#3" accession="ERX1416129" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416129</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_5#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_5#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362748, constructed from sample accession ERS474309 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_5).  This submission includes reads tagged with the sequence ACAGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474309">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474309</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581069</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362748</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_5#4" accession="ERX1416130" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416130</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_5#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_5#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362749, constructed from sample accession ERS474324 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_5).  This submission includes reads tagged with the sequence AGATGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474324">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474324</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581084</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362749</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_5#5" accession="ERX1416131" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416131</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_5#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_5#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362750, constructed from sample accession ERS474335 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_5).  This submission includes reads tagged with the sequence AGCACCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474335">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474335</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581095</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362750</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_5#6" accession="ERX1416132" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416132</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_5#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_5#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362751, constructed from sample accession ERS474343 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_5).  This submission includes reads tagged with the sequence AGCCATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474343">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474343</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581103</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362751</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_5#7" accession="ERX1416133" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416133</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_5#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_5#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362752, constructed from sample accession ERS474353 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_5).  This submission includes reads tagged with the sequence AGGCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474353">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474353</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581113</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362752</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_5#8" accession="ERX1416134" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416134</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_5#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_5#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362753, constructed from sample accession ERS474366 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_5).  This submission includes reads tagged with the sequence ATAGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474366">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474366</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581126</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362753</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_5#9" accession="ERX1416135" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416135</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_5#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_5#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362754, constructed from sample accession ERS474374 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_5).  This submission includes reads tagged with the sequence ATCATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474374">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474374</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581134</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362754</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_5#10" accession="ERX1416136" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416136</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_5#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_5#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362755, constructed from sample accession ERS474389 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_5).  This submission includes reads tagged with the sequence ATTGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474389">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474389</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581149</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362755</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_5#11" accession="ERX1416137" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416137</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_5#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_5#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362756, constructed from sample accession ERS474400 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_5).  This submission includes reads tagged with the sequence CAAGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474400">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474400</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581160</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362756</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_5#12" accession="ERX1416138" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416138</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_5#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_5#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362757, constructed from sample accession ERS474421 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_5).  This submission includes reads tagged with the sequence CACCTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474421">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474421</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581181</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362757</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="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_6#1" accession="ERX1416139" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416139</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_6#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_6#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362746, constructed from sample accession ERS474280 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_6).  This submission includes reads tagged with the sequence AATGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474280">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474280</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581040</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362746</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_6#2" accession="ERX1416140" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416140</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_6#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_6#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362747, constructed from sample accession ERS474295 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_6).  This submission includes reads tagged with the sequence ACACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474295">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474295</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581055</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362747</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_6#3" accession="ERX1416141" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416141</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_6#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_6#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362748, constructed from sample accession ERS474309 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_6).  This submission includes reads tagged with the sequence ACAGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474309">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474309</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581069</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362748</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_6#4" accession="ERX1416142" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416142</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_6#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_6#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362749, constructed from sample accession ERS474324 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_6).  This submission includes reads tagged with the sequence AGATGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474324">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474324</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581084</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362749</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_6#5" accession="ERX1416143" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416143</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_6#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_6#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362750, constructed from sample accession ERS474335 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_6).  This submission includes reads tagged with the sequence AGCACCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474335">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474335</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581095</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362750</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_6#6" accession="ERX1416144" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416144</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_6#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_6#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362751, constructed from sample accession ERS474343 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_6).  This submission includes reads tagged with the sequence AGCCATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474343">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474343</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581103</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362751</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_6#7" accession="ERX1416145" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416145</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_6#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_6#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362752, constructed from sample accession ERS474353 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_6).  This submission includes reads tagged with the sequence AGGCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474353">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474353</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581113</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362752</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_6#8" accession="ERX1416146" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416146</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_6#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_6#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362753, constructed from sample accession ERS474366 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_6).  This submission includes reads tagged with the sequence ATAGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474366">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474366</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581126</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362753</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_6#9" accession="ERX1416147" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416147</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_6#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_6#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362754, constructed from sample accession ERS474374 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_6).  This submission includes reads tagged with the sequence ATCATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474374">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474374</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581134</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362754</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_6#10" accession="ERX1416148" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416148</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_6#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_6#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362755, constructed from sample accession ERS474389 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_6).  This submission includes reads tagged with the sequence ATTGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474389">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474389</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581149</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362755</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_6#11" accession="ERX1416149" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416149</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_6#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_6#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362756, constructed from sample accession ERS474400 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_6).  This submission includes reads tagged with the sequence CAAGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474400">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474400</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581160</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362756</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_6#12" accession="ERX1416150" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416150</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_6#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_6#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362757, constructed from sample accession ERS474421 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_6).  This submission includes reads tagged with the sequence CACCTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474421">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474421</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581181</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362757</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_7#1" accession="ERX1416151" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416151</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_7#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_7#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362746, constructed from sample accession ERS474280 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_7).  This submission includes reads tagged with the sequence AATGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474280">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474280</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581040</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362746</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_7#2" accession="ERX1416152" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416152</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_7#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_7#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362747, constructed from sample accession ERS474295 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_7).  This submission includes reads tagged with the sequence ACACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474295">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474295</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581055</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362747</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_7#3" accession="ERX1416153" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416153</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_7#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_7#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362748, constructed from sample accession ERS474309 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_7).  This submission includes reads tagged with the sequence ACAGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474309">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474309</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581069</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362748</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_7#4" accession="ERX1416154" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416154</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_7#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_7#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362749, constructed from sample accession ERS474324 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_7).  This submission includes reads tagged with the sequence AGATGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474324">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474324</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581084</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362749</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_7#5" accession="ERX1416155" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416155</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_7#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_7#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362750, constructed from sample accession ERS474335 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_7).  This submission includes reads tagged with the sequence AGCACCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474335">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474335</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581095</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362750</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_7#6" accession="ERX1416156" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416156</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_7#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_7#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362751, constructed from sample accession ERS474343 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_7).  This submission includes reads tagged with the sequence AGCCATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474343">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474343</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581103</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362751</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_7#7" accession="ERX1416157" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416157</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_7#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_7#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362752, constructed from sample accession ERS474353 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_7).  This submission includes reads tagged with the sequence AGGCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474353">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474353</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581113</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362752</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_7#8" accession="ERX1416158" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416158</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_7#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_7#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362753, constructed from sample accession ERS474366 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_7).  This submission includes reads tagged with the sequence ATAGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474366">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474366</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581126</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362753</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_7#9" accession="ERX1416159" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416159</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_7#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_7#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362754, constructed from sample accession ERS474374 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_7).  This submission includes reads tagged with the sequence ATCATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474374">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474374</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581134</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362754</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_7#10" accession="ERX1416160" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416160</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_7#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_7#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362755, constructed from sample accession ERS474389 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_7).  This submission includes reads tagged with the sequence ATTGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474389">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474389</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581149</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362755</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_7#11" accession="ERX1416161" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416161</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_7#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_7#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362756, constructed from sample accession ERS474400 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_7).  This submission includes reads tagged with the sequence CAAGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474400">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474400</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581160</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362756</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_7#12" accession="ERX1416162" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416162</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_7#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_7#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362757, constructed from sample accession ERS474421 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_7).  This submission includes reads tagged with the sequence CACCTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474421">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474421</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581181</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362757</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_8#1" accession="ERX1416163" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416163</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_8#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_8#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362746, constructed from sample accession ERS474280 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_8).  This submission includes reads tagged with the sequence AATGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474280">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474280</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581040</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362746</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_8#2" accession="ERX1416164" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416164</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_8#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_8#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362747, constructed from sample accession ERS474295 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_8).  This submission includes reads tagged with the sequence ACACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474295">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474295</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581055</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362747</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_8#3" accession="ERX1416165" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416165</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_8#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_8#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362748, constructed from sample accession ERS474309 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_8).  This submission includes reads tagged with the sequence ACAGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474309">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474309</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581069</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362748</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_8#4" accession="ERX1416166" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416166</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_8#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_8#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362749, constructed from sample accession ERS474324 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_8).  This submission includes reads tagged with the sequence AGATGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474324">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474324</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581084</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362749</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_8#5" accession="ERX1416167" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416167</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_8#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_8#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362750, constructed from sample accession ERS474335 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_8).  This submission includes reads tagged with the sequence AGCACCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474335">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474335</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581095</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362750</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_8#6" accession="ERX1416168" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416168</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_8#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_8#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362751, constructed from sample accession ERS474343 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_8).  This submission includes reads tagged with the sequence AGCCATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474343">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474343</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581103</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362751</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_8#7" accession="ERX1416169" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416169</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_8#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_8#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362752, constructed from sample accession ERS474353 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_8).  This submission includes reads tagged with the sequence AGGCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474353">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474353</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581113</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362752</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_8#8" accession="ERX1416170" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416170</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_8#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_8#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362753, constructed from sample accession ERS474366 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_8).  This submission includes reads tagged with the sequence ATAGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474366">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474366</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581126</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362753</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_8#9" accession="ERX1416171" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416171</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_8#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_8#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362754, constructed from sample accession ERS474374 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_8).  This submission includes reads tagged with the sequence ATCATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474374">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474374</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581134</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362754</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_8#10" accession="ERX1416172" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416172</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_8#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_8#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362755, constructed from sample accession ERS474389 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_8).  This submission includes reads tagged with the sequence ATTGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474389">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474389</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581149</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362755</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_8#11" accession="ERX1416173" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416173</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_8#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_8#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362756, constructed from sample accession ERS474400 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_8).  This submission includes reads tagged with the sequence CAAGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474400">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474400</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581160</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362756</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18662_8#12" accession="ERX1416174" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416174</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18662_8#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18662_8#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362757, constructed from sample accession ERS474421 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18662_8).  This submission includes reads tagged with the sequence CACCTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474421">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474421</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581181</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362757</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_1#1" accession="ERX1416175" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416175</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362698, constructed from sample accession ERS474276 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_1).  This submission includes reads tagged with the sequence AGATCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474276">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474276</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581036</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362698</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="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_1#2" accession="ERX1416176" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416176</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362699, constructed from sample accession ERS474290 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_1).  This submission includes reads tagged with the sequence AGCAGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474290">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474290</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581050</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362699</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="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_1#3" accession="ERX1416177" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416177</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362700, constructed from sample accession ERS474304 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_1).  This submission includes reads tagged with the sequence AGTCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474304">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581064</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362700</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="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_1#4" accession="ERX1416178" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416178</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362701, constructed from sample accession ERS474314 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_1).  This submission includes reads tagged with the sequence ATCCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474314">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474314</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581074</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362701</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="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_1#5" accession="ERX1416179" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416179</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362702, constructed from sample accession ERS474329 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_1).  This submission includes reads tagged with the sequence ATTGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474329">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474329</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581089</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362702</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="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_1#6" accession="ERX1416180" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416180</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_1#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_1#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362703, constructed from sample accession ERS474339 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_1).  This submission includes reads tagged with the sequence CAACCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474339">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474339</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581099</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362703</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="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_1#7" accession="ERX1416181" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416181</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362704, constructed from sample accession ERS474348 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_1).  This submission includes reads tagged with the sequence GACTAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474348">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581108</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362704</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="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_1#8" accession="ERX1416182" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416182</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_1#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_1#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362705, constructed from sample accession ERS474361 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_1).  This submission includes reads tagged with the sequence CAATGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474361">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474361</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581121</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362705</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="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_1#9" accession="ERX1416183" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416183</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_1#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_1#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362706, constructed from sample accession ERS474370 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_1).  This submission includes reads tagged with the sequence CACTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474370">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474370</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581130</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362706</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="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_1#10" accession="ERX1416184" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416184</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_1#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_1#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362707, constructed from sample accession ERS474378 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_1).  This submission includes reads tagged with the sequence CAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474378">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474378</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581138</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362707</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="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_1#11" accession="ERX1416185" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416185</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_1#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_1#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362708, constructed from sample accession ERS474395 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_1).  This submission includes reads tagged with the sequence CATACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474395">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474395</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581155</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362708</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="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_1#12" accession="ERX1416186" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416186</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_1#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_1#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362709, constructed from sample accession ERS474416 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_1).  This submission includes reads tagged with the sequence CCAGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474416">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474416</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581176</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362709</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="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_2#1" accession="ERX1416187" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416187</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362698, constructed from sample accession ERS474276 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_2).  This submission includes reads tagged with the sequence AGATCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474276">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474276</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581036</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362698</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_2#2" accession="ERX1416188" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416188</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362699, constructed from sample accession ERS474290 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_2).  This submission includes reads tagged with the sequence AGCAGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474290">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474290</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581050</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362699</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_2#3" accession="ERX1416189" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416189</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362700, constructed from sample accession ERS474304 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_2).  This submission includes reads tagged with the sequence AGTCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474304">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581064</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362700</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_2#4" accession="ERX1416190" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416190</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362701, constructed from sample accession ERS474314 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_2).  This submission includes reads tagged with the sequence ATCCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474314">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474314</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581074</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362701</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_2#5" accession="ERX1416191" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416191</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362702, constructed from sample accession ERS474329 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_2).  This submission includes reads tagged with the sequence ATTGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474329">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474329</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581089</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362702</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_2#6" accession="ERX1416192" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416192</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362703, constructed from sample accession ERS474339 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_2).  This submission includes reads tagged with the sequence CAACCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474339">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474339</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581099</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362703</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_2#7" accession="ERX1416193" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416193</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_2#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_2#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362704, constructed from sample accession ERS474348 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_2).  This submission includes reads tagged with the sequence GACTAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474348">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581108</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362704</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_2#8" accession="ERX1416194" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416194</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_2#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_2#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362705, constructed from sample accession ERS474361 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_2).  This submission includes reads tagged with the sequence CAATGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474361">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474361</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581121</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362705</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_2#9" accession="ERX1416195" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416195</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_2#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_2#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362706, constructed from sample accession ERS474370 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_2).  This submission includes reads tagged with the sequence CACTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474370">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474370</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581130</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362706</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_2#10" accession="ERX1416196" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416196</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_2#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_2#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362707, constructed from sample accession ERS474378 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_2).  This submission includes reads tagged with the sequence CAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474378">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474378</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581138</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362707</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_2#11" accession="ERX1416197" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416197</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_2#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_2#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362708, constructed from sample accession ERS474395 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_2).  This submission includes reads tagged with the sequence CATACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474395">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474395</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581155</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362708</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_2#12" accession="ERX1416198" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416198</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_2#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_2#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362709, constructed from sample accession ERS474416 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_2).  This submission includes reads tagged with the sequence CCAGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474416">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474416</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581176</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362709</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_3#1" accession="ERX1416199" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416199</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_3#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_3#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362698, constructed from sample accession ERS474276 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_3).  This submission includes reads tagged with the sequence AGATCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474276">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474276</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581036</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362698</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_3#2" accession="ERX1416200" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416200</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_3#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_3#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362699, constructed from sample accession ERS474290 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_3).  This submission includes reads tagged with the sequence AGCAGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474290">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474290</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581050</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362699</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_3#3" accession="ERX1416201" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416201</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_3#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_3#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362700, constructed from sample accession ERS474304 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_3).  This submission includes reads tagged with the sequence AGTCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474304">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581064</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362700</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_3#4" accession="ERX1416202" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416202</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_3#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_3#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362701, constructed from sample accession ERS474314 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_3).  This submission includes reads tagged with the sequence ATCCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474314">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474314</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581074</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362701</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_3#5" accession="ERX1416203" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416203</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_3#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_3#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362702, constructed from sample accession ERS474329 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_3).  This submission includes reads tagged with the sequence ATTGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474329">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474329</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581089</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362702</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_3#6" accession="ERX1416204" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416204</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_3#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_3#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362703, constructed from sample accession ERS474339 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_3).  This submission includes reads tagged with the sequence CAACCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474339">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474339</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581099</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362703</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_3#7" accession="ERX1416205" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416205</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_3#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_3#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362704, constructed from sample accession ERS474348 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_3).  This submission includes reads tagged with the sequence GACTAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474348">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581108</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362704</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_3#8" accession="ERX1416206" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416206</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_3#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_3#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362705, constructed from sample accession ERS474361 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_3).  This submission includes reads tagged with the sequence CAATGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474361">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474361</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581121</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362705</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_3#9" accession="ERX1416207" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416207</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_3#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_3#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362706, constructed from sample accession ERS474370 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_3).  This submission includes reads tagged with the sequence CACTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474370">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474370</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581130</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362706</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_3#10" accession="ERX1416208" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416208</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_3#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_3#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362707, constructed from sample accession ERS474378 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_3).  This submission includes reads tagged with the sequence CAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474378">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474378</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581138</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362707</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_3#11" accession="ERX1416209" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416209</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_3#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_3#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362708, constructed from sample accession ERS474395 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_3).  This submission includes reads tagged with the sequence CATACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474395">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474395</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581155</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362708</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_3#12" accession="ERX1416210" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416210</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_3#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_3#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362709, constructed from sample accession ERS474416 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_3).  This submission includes reads tagged with the sequence CCAGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474416">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474416</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581176</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362709</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_4#1" accession="ERX1416211" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416211</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_4#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_4#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362698, constructed from sample accession ERS474276 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_4).  This submission includes reads tagged with the sequence AGATCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474276">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474276</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581036</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362698</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_4#2" accession="ERX1416212" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416212</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_4#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_4#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362699, constructed from sample accession ERS474290 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_4).  This submission includes reads tagged with the sequence AGCAGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474290">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474290</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581050</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362699</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_4#3" accession="ERX1416213" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416213</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_4#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_4#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362700, constructed from sample accession ERS474304 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_4).  This submission includes reads tagged with the sequence AGTCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474304">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581064</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362700</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_4#4" accession="ERX1416214" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416214</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_4#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_4#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362701, constructed from sample accession ERS474314 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_4).  This submission includes reads tagged with the sequence ATCCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474314">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474314</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581074</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362701</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_4#5" accession="ERX1416215" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416215</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_4#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_4#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362702, constructed from sample accession ERS474329 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_4).  This submission includes reads tagged with the sequence ATTGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474329">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474329</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581089</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362702</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_4#6" accession="ERX1416216" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416216</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_4#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_4#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362703, constructed from sample accession ERS474339 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_4).  This submission includes reads tagged with the sequence CAACCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474339">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474339</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581099</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362703</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_4#7" accession="ERX1416217" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416217</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_4#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_4#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362704, constructed from sample accession ERS474348 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_4).  This submission includes reads tagged with the sequence GACTAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474348">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581108</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362704</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_4#8" accession="ERX1416218" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416218</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_4#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_4#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362705, constructed from sample accession ERS474361 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_4).  This submission includes reads tagged with the sequence CAATGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474361">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474361</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581121</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362705</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_4#9" accession="ERX1416219" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416219</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_4#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_4#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362706, constructed from sample accession ERS474370 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_4).  This submission includes reads tagged with the sequence CACTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474370">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474370</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581130</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362706</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_4#10" accession="ERX1416220" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416220</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_4#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_4#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362707, constructed from sample accession ERS474378 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_4).  This submission includes reads tagged with the sequence CAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474378">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474378</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581138</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362707</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_4#11" accession="ERX1416221" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416221</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_4#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_4#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362708, constructed from sample accession ERS474395 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_4).  This submission includes reads tagged with the sequence CATACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474395">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474395</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581155</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362708</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_4#12" accession="ERX1416222" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416222</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_4#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_4#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362709, constructed from sample accession ERS474416 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_4).  This submission includes reads tagged with the sequence CCAGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474416">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474416</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581176</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362709</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_5#1" accession="ERX1416223" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416223</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_5#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_5#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362698, constructed from sample accession ERS474276 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_5).  This submission includes reads tagged with the sequence AGATCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474276">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474276</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581036</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362698</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_5#2" accession="ERX1416224" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416224</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_5#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_5#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362699, constructed from sample accession ERS474290 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_5).  This submission includes reads tagged with the sequence AGCAGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474290">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474290</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581050</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362699</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_5#3" accession="ERX1416225" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416225</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_5#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_5#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362700, constructed from sample accession ERS474304 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_5).  This submission includes reads tagged with the sequence AGTCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474304">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581064</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362700</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_5#4" accession="ERX1416226" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416226</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_5#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_5#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362701, constructed from sample accession ERS474314 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_5).  This submission includes reads tagged with the sequence ATCCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474314">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474314</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581074</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362701</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_5#5" accession="ERX1416227" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416227</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_5#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_5#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362702, constructed from sample accession ERS474329 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_5).  This submission includes reads tagged with the sequence ATTGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474329">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474329</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581089</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362702</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_5#6" accession="ERX1416228" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416228</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_5#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_5#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362703, constructed from sample accession ERS474339 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_5).  This submission includes reads tagged with the sequence CAACCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474339">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474339</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581099</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362703</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_5#7" accession="ERX1416229" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416229</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_5#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_5#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362704, constructed from sample accession ERS474348 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_5).  This submission includes reads tagged with the sequence GACTAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474348">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581108</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362704</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_5#8" accession="ERX1416230" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416230</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_5#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_5#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362705, constructed from sample accession ERS474361 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_5).  This submission includes reads tagged with the sequence CAATGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474361">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474361</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581121</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362705</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_5#9" accession="ERX1416231" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416231</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_5#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_5#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362706, constructed from sample accession ERS474370 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_5).  This submission includes reads tagged with the sequence CACTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474370">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474370</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581130</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362706</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_5#10" accession="ERX1416232" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416232</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_5#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_5#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362707, constructed from sample accession ERS474378 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_5).  This submission includes reads tagged with the sequence CAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474378">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474378</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581138</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362707</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_5#11" accession="ERX1416233" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416233</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_5#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_5#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362708, constructed from sample accession ERS474395 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_5).  This submission includes reads tagged with the sequence CATACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474395">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474395</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581155</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362708</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_5#12" accession="ERX1416234" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416234</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_5#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_5#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362709, constructed from sample accession ERS474416 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_5).  This submission includes reads tagged with the sequence CCAGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474416">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474416</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581176</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362709</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_6#1" accession="ERX1416235" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416235</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_6#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_6#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362698, constructed from sample accession ERS474276 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_6).  This submission includes reads tagged with the sequence AGATCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474276">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474276</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581036</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362698</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_6#2" accession="ERX1416236" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416236</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_6#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_6#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362699, constructed from sample accession ERS474290 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_6).  This submission includes reads tagged with the sequence AGCAGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474290">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474290</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581050</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362699</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_6#3" accession="ERX1416237" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416237</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_6#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_6#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362700, constructed from sample accession ERS474304 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_6).  This submission includes reads tagged with the sequence AGTCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474304">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581064</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362700</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_6#4" accession="ERX1416238" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416238</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_6#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_6#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362701, constructed from sample accession ERS474314 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_6).  This submission includes reads tagged with the sequence ATCCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474314">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474314</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581074</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362701</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_6#5" accession="ERX1416239" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416239</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_6#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_6#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362702, constructed from sample accession ERS474329 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_6).  This submission includes reads tagged with the sequence ATTGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474329">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474329</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581089</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362702</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_6#6" accession="ERX1416240" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416240</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_6#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_6#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362703, constructed from sample accession ERS474339 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_6).  This submission includes reads tagged with the sequence CAACCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474339">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474339</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581099</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362703</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_6#7" accession="ERX1416241" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416241</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_6#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_6#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362704, constructed from sample accession ERS474348 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_6).  This submission includes reads tagged with the sequence GACTAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474348">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581108</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362704</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_6#8" accession="ERX1416242" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416242</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_6#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_6#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362705, constructed from sample accession ERS474361 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_6).  This submission includes reads tagged with the sequence CAATGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474361">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474361</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581121</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362705</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_6#9" accession="ERX1416243" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416243</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_6#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_6#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362706, constructed from sample accession ERS474370 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_6).  This submission includes reads tagged with the sequence CACTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474370">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474370</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581130</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362706</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_6#10" accession="ERX1416244" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416244</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_6#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_6#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362707, constructed from sample accession ERS474378 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_6).  This submission includes reads tagged with the sequence CAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474378">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474378</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581138</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362707</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_6#11" accession="ERX1416245" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416245</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_6#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_6#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362708, constructed from sample accession ERS474395 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_6).  This submission includes reads tagged with the sequence CATACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474395">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474395</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581155</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362708</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_6#12" accession="ERX1416246" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416246</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_6#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_6#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362709, constructed from sample accession ERS474416 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_6).  This submission includes reads tagged with the sequence CCAGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474416">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474416</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581176</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362709</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_7#1" accession="ERX1416247" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416247</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_7#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_7#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362698, constructed from sample accession ERS474276 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_7).  This submission includes reads tagged with the sequence AGATCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474276">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474276</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581036</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362698</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_7#2" accession="ERX1416248" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416248</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_7#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_7#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362699, constructed from sample accession ERS474290 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_7).  This submission includes reads tagged with the sequence AGCAGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474290">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474290</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581050</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362699</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_7#3" accession="ERX1416249" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416249</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_7#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_7#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362700, constructed from sample accession ERS474304 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_7).  This submission includes reads tagged with the sequence AGTCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474304">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581064</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362700</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_7#4" accession="ERX1416250" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416250</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_7#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_7#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362701, constructed from sample accession ERS474314 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_7).  This submission includes reads tagged with the sequence ATCCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474314">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474314</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581074</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362701</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_7#5" accession="ERX1416251" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416251</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_7#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_7#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362702, constructed from sample accession ERS474329 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_7).  This submission includes reads tagged with the sequence ATTGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474329">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474329</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581089</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362702</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_7#6" accession="ERX1416252" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416252</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_7#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_7#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362703, constructed from sample accession ERS474339 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_7).  This submission includes reads tagged with the sequence CAACCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474339">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474339</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581099</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362703</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_7#7" accession="ERX1416253" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416253</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_7#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_7#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362704, constructed from sample accession ERS474348 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_7).  This submission includes reads tagged with the sequence GACTAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474348">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581108</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362704</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_7#8" accession="ERX1416254" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416254</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_7#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_7#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362705, constructed from sample accession ERS474361 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_7).  This submission includes reads tagged with the sequence CAATGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474361">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474361</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581121</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362705</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_7#9" accession="ERX1416255" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416255</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_7#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_7#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362706, constructed from sample accession ERS474370 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_7).  This submission includes reads tagged with the sequence CACTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474370">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474370</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581130</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362706</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_7#10" accession="ERX1416256" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416256</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_7#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_7#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362707, constructed from sample accession ERS474378 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_7).  This submission includes reads tagged with the sequence CAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474378">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474378</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581138</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362707</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_7#11" accession="ERX1416257" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416257</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_7#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_7#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362708, constructed from sample accession ERS474395 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_7).  This submission includes reads tagged with the sequence CATACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474395">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474395</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581155</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362708</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_7#12" accession="ERX1416258" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416258</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_7#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_7#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362709, constructed from sample accession ERS474416 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_7).  This submission includes reads tagged with the sequence CCAGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474416">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474416</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581176</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362709</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_8#1" accession="ERX1416259" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416259</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_8#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_8#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362698, constructed from sample accession ERS474276 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_8).  This submission includes reads tagged with the sequence AGATCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474276">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474276</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581036</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362698</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_8#2" accession="ERX1416260" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416260</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_8#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_8#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362699, constructed from sample accession ERS474290 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_8).  This submission includes reads tagged with the sequence AGCAGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474290">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474290</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581050</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362699</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_8#3" accession="ERX1416261" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416261</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_8#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_8#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362700, constructed from sample accession ERS474304 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_8).  This submission includes reads tagged with the sequence AGTCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474304">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581064</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362700</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_8#4" accession="ERX1416262" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416262</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_8#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_8#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362701, constructed from sample accession ERS474314 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_8).  This submission includes reads tagged with the sequence ATCCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474314">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474314</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581074</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362701</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_8#5" accession="ERX1416263" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416263</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_8#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_8#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362702, constructed from sample accession ERS474329 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_8).  This submission includes reads tagged with the sequence ATTGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474329">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474329</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581089</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362702</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_8#6" accession="ERX1416264" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416264</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_8#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_8#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362703, constructed from sample accession ERS474339 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_8).  This submission includes reads tagged with the sequence CAACCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474339">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474339</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581099</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362703</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_8#7" accession="ERX1416265" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416265</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_8#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_8#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362704, constructed from sample accession ERS474348 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_8).  This submission includes reads tagged with the sequence GACTAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474348">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581108</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362704</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_8#8" accession="ERX1416266" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416266</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_8#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_8#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362705, constructed from sample accession ERS474361 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_8).  This submission includes reads tagged with the sequence CAATGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474361">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474361</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581121</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362705</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_8#9" accession="ERX1416267" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416267</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_8#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_8#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362706, constructed from sample accession ERS474370 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_8).  This submission includes reads tagged with the sequence CACTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474370">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474370</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581130</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362706</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_8#10" accession="ERX1416268" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416268</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_8#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_8#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362707, constructed from sample accession ERS474378 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_8).  This submission includes reads tagged with the sequence CAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474378">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474378</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581138</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362707</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_8#11" accession="ERX1416269" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416269</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_8#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_8#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362708, constructed from sample accession ERS474395 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_8).  This submission includes reads tagged with the sequence CATACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474395">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474395</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581155</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362708</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18671_8#12" accession="ERX1416270" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416270</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18671_8#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18671_8#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362709, constructed from sample accession ERS474416 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18671_8).  This submission includes reads tagged with the sequence CCAGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474416">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474416</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581176</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362709</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_1#1" accession="ERX1416271" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416271</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362734, constructed from sample accession ERS474279 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_1).  This submission includes reads tagged with the sequence TATCAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474279">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474279</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581039</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362734</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_1#2" accession="ERX1416272" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416272</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362735, constructed from sample accession ERS474294 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_1).  This submission includes reads tagged with the sequence TCCGTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474294">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474294</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581054</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362735</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_1#3" accession="ERX1416273" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416273</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362736, constructed from sample accession ERS474308 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_1).  This submission includes reads tagged with the sequence TCTTCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474308">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474308</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581068</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362736</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_1#4" accession="ERX1416274" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416274</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362737, constructed from sample accession ERS474322 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_1).  This submission includes reads tagged with the sequence TGAAGAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474322">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474322</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581082</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362737</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_1#5" accession="ERX1416275" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416275</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362738, constructed from sample accession ERS474334 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_1).  This submission includes reads tagged with the sequence TGGAACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474334">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474334</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581094</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362738</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_1#6" accession="ERX1416276" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416276</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_1#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_1#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362739, constructed from sample accession ERS474342 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_1).  This submission includes reads tagged with the sequence TGGCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474342">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474342</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581102</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362739</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_1#7" accession="ERX1416277" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416277</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362740, constructed from sample accession ERS474352 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_1).  This submission includes reads tagged with the sequence TGGTGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474352">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581112</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362740</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_1#8" accession="ERX1416278" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416278</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_1#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_1#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362741, constructed from sample accession ERS474364 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_1).  This submission includes reads tagged with the sequence TTCACGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474364">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474364</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581124</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362741</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_1#9" accession="ERX1416279" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416279</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_1#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_1#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362742, constructed from sample accession ERS474373 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_1).  This submission includes reads tagged with the sequence AACTCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474373">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474373</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581133</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362742</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_1#10" accession="ERX1416280" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416280</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_1#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_1#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362743, constructed from sample accession ERS474387 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_1).  This submission includes reads tagged with the sequence AAGAGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474387">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474387</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581147</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362743</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_1#11" accession="ERX1416281" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416281</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_1#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_1#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362744, constructed from sample accession ERS474398 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_1).  This submission includes reads tagged with the sequence AAGGACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474398">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474398</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581158</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362744</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_1#12" accession="ERX1416282" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416282</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_1#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_1#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362745, constructed from sample accession ERS474420 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_1).  This submission includes reads tagged with the sequence AATCCGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474420">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474420</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581180</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362745</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_2#1" accession="ERX1416283" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416283</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362734, constructed from sample accession ERS474279 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_2).  This submission includes reads tagged with the sequence TATCAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474279">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474279</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581039</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362734</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_2#2" accession="ERX1416284" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416284</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362735, constructed from sample accession ERS474294 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_2).  This submission includes reads tagged with the sequence TCCGTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474294">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474294</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581054</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362735</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_2#3" accession="ERX1416285" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416285</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362736, constructed from sample accession ERS474308 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_2).  This submission includes reads tagged with the sequence TCTTCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474308">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474308</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581068</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362736</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_2#4" accession="ERX1416286" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416286</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362737, constructed from sample accession ERS474322 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_2).  This submission includes reads tagged with the sequence TGAAGAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474322">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474322</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581082</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362737</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_2#5" accession="ERX1416287" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416287</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362738, constructed from sample accession ERS474334 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_2).  This submission includes reads tagged with the sequence TGGAACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474334">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474334</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581094</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362738</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_2#6" accession="ERX1416288" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416288</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362739, constructed from sample accession ERS474342 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_2).  This submission includes reads tagged with the sequence TGGCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474342">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474342</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581102</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362739</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_2#7" accession="ERX1416289" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416289</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_2#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_2#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362740, constructed from sample accession ERS474352 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_2).  This submission includes reads tagged with the sequence TGGTGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474352">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581112</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362740</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_2#8" accession="ERX1416290" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416290</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_2#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_2#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362741, constructed from sample accession ERS474364 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_2).  This submission includes reads tagged with the sequence TTCACGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474364">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474364</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581124</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362741</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_2#9" accession="ERX1416291" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416291</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_2#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_2#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362742, constructed from sample accession ERS474373 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_2).  This submission includes reads tagged with the sequence AACTCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474373">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474373</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581133</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362742</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_2#10" accession="ERX1416292" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416292</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_2#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_2#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362743, constructed from sample accession ERS474387 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_2).  This submission includes reads tagged with the sequence AAGAGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474387">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474387</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581147</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362743</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_2#11" accession="ERX1416293" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416293</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_2#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_2#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362744, constructed from sample accession ERS474398 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_2).  This submission includes reads tagged with the sequence AAGGACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474398">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474398</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581158</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362744</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_2#12" accession="ERX1416294" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416294</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_2#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_2#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362745, constructed from sample accession ERS474420 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_2).  This submission includes reads tagged with the sequence AATCCGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474420">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474420</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581180</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362745</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_3#1" accession="ERX1416295" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416295</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_3#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_3#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362734, constructed from sample accession ERS474279 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_3).  This submission includes reads tagged with the sequence TATCAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474279">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474279</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581039</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362734</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_3#2" accession="ERX1416296" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416296</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_3#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_3#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362735, constructed from sample accession ERS474294 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_3).  This submission includes reads tagged with the sequence TCCGTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474294">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474294</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581054</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362735</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_3#3" accession="ERX1416297" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416297</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_3#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_3#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362736, constructed from sample accession ERS474308 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_3).  This submission includes reads tagged with the sequence TCTTCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474308">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474308</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581068</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362736</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_3#4" accession="ERX1416298" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416298</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_3#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_3#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362737, constructed from sample accession ERS474322 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_3).  This submission includes reads tagged with the sequence TGAAGAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474322">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474322</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581082</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362737</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_3#5" accession="ERX1416299" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416299</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_3#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_3#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362738, constructed from sample accession ERS474334 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_3).  This submission includes reads tagged with the sequence TGGAACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474334">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474334</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581094</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362738</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_3#6" accession="ERX1416300" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416300</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_3#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_3#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362739, constructed from sample accession ERS474342 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_3).  This submission includes reads tagged with the sequence TGGCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474342">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474342</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581102</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362739</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_3#7" accession="ERX1416301" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416301</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_3#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_3#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362740, constructed from sample accession ERS474352 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_3).  This submission includes reads tagged with the sequence TGGTGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474352">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581112</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362740</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_3#8" accession="ERX1416302" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416302</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_3#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_3#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362741, constructed from sample accession ERS474364 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_3).  This submission includes reads tagged with the sequence TTCACGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474364">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474364</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581124</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362741</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_3#9" accession="ERX1416303" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416303</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_3#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_3#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362742, constructed from sample accession ERS474373 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_3).  This submission includes reads tagged with the sequence AACTCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474373">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474373</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581133</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362742</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_3#10" accession="ERX1416304" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416304</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_3#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_3#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362743, constructed from sample accession ERS474387 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_3).  This submission includes reads tagged with the sequence AAGAGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474387">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474387</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581147</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362743</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_3#11" accession="ERX1416305" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416305</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_3#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_3#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362744, constructed from sample accession ERS474398 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_3).  This submission includes reads tagged with the sequence AAGGACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474398">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474398</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581158</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362744</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_3#12" accession="ERX1416306" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416306</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_3#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_3#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362745, constructed from sample accession ERS474420 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_3).  This submission includes reads tagged with the sequence AATCCGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474420">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474420</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581180</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362745</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_4#1" accession="ERX1416307" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416307</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_4#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_4#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362734, constructed from sample accession ERS474279 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_4).  This submission includes reads tagged with the sequence TATCAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474279">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474279</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581039</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362734</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_4#2" accession="ERX1416308" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416308</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_4#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_4#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362735, constructed from sample accession ERS474294 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_4).  This submission includes reads tagged with the sequence TCCGTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474294">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474294</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581054</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362735</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_4#3" accession="ERX1416309" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416309</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_4#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_4#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362736, constructed from sample accession ERS474308 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_4).  This submission includes reads tagged with the sequence TCTTCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474308">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474308</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581068</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362736</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_4#4" accession="ERX1416310" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416310</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_4#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_4#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362737, constructed from sample accession ERS474322 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_4).  This submission includes reads tagged with the sequence TGAAGAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474322">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474322</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581082</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362737</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_4#5" accession="ERX1416311" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416311</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_4#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_4#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362738, constructed from sample accession ERS474334 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_4).  This submission includes reads tagged with the sequence TGGAACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474334">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474334</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581094</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362738</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_4#6" accession="ERX1416312" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416312</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_4#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_4#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362739, constructed from sample accession ERS474342 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_4).  This submission includes reads tagged with the sequence TGGCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474342">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474342</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581102</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362739</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_4#7" accession="ERX1416313" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416313</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_4#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_4#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362740, constructed from sample accession ERS474352 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_4).  This submission includes reads tagged with the sequence TGGTGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474352">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581112</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362740</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_4#8" accession="ERX1416314" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416314</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_4#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_4#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362741, constructed from sample accession ERS474364 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_4).  This submission includes reads tagged with the sequence TTCACGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474364">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474364</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581124</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362741</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_4#9" accession="ERX1416315" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416315</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_4#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_4#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362742, constructed from sample accession ERS474373 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_4).  This submission includes reads tagged with the sequence AACTCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474373">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474373</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581133</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362742</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_4#10" accession="ERX1416316" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416316</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_4#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_4#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362743, constructed from sample accession ERS474387 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_4).  This submission includes reads tagged with the sequence AAGAGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474387">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474387</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581147</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362743</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_4#11" accession="ERX1416317" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416317</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_4#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_4#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362744, constructed from sample accession ERS474398 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_4).  This submission includes reads tagged with the sequence AAGGACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474398">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474398</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581158</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362744</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_4#12" accession="ERX1416318" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416318</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_4#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_4#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362745, constructed from sample accession ERS474420 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_4).  This submission includes reads tagged with the sequence AATCCGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474420">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474420</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581180</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362745</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="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_5#1" accession="ERX1416319" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416319</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_5#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_5#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362734, constructed from sample accession ERS474279 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_5).  This submission includes reads tagged with the sequence TATCAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474279">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474279</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581039</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362734</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_5#2" accession="ERX1416320" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416320</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_5#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_5#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362735, constructed from sample accession ERS474294 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_5).  This submission includes reads tagged with the sequence TCCGTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474294">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474294</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581054</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362735</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_5#3" accession="ERX1416321" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416321</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_5#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_5#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362736, constructed from sample accession ERS474308 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_5).  This submission includes reads tagged with the sequence TCTTCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474308">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474308</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581068</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362736</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_5#4" accession="ERX1416322" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416322</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_5#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_5#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362737, constructed from sample accession ERS474322 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_5).  This submission includes reads tagged with the sequence TGAAGAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474322">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474322</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581082</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362737</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_5#5" accession="ERX1416323" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416323</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_5#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_5#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362738, constructed from sample accession ERS474334 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_5).  This submission includes reads tagged with the sequence TGGAACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474334">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474334</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581094</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362738</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_5#6" accession="ERX1416324" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416324</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_5#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_5#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362739, constructed from sample accession ERS474342 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_5).  This submission includes reads tagged with the sequence TGGCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474342">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474342</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581102</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362739</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_5#7" accession="ERX1416325" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416325</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_5#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_5#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362740, constructed from sample accession ERS474352 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_5).  This submission includes reads tagged with the sequence TGGTGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474352">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581112</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362740</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_5#8" accession="ERX1416326" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416326</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_5#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_5#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362741, constructed from sample accession ERS474364 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_5).  This submission includes reads tagged with the sequence TTCACGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474364">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474364</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581124</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362741</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_5#9" accession="ERX1416327" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416327</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_5#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_5#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362742, constructed from sample accession ERS474373 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_5).  This submission includes reads tagged with the sequence AACTCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474373">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474373</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581133</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362742</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_5#10" accession="ERX1416328" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416328</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_5#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_5#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362743, constructed from sample accession ERS474387 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_5).  This submission includes reads tagged with the sequence AAGAGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474387">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474387</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581147</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362743</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_5#11" accession="ERX1416329" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416329</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_5#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_5#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362744, constructed from sample accession ERS474398 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_5).  This submission includes reads tagged with the sequence AAGGACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474398">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474398</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581158</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362744</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_5#12" accession="ERX1416330" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416330</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_5#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_5#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362745, constructed from sample accession ERS474420 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_5).  This submission includes reads tagged with the sequence AATCCGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474420">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474420</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581180</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362745</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_6#1" accession="ERX1416331" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416331</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_6#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_6#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362734, constructed from sample accession ERS474279 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_6).  This submission includes reads tagged with the sequence TATCAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474279">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474279</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581039</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362734</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_6#2" accession="ERX1416332" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416332</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_6#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_6#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362735, constructed from sample accession ERS474294 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_6).  This submission includes reads tagged with the sequence TCCGTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474294">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474294</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581054</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362735</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_6#3" accession="ERX1416333" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416333</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_6#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_6#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362736, constructed from sample accession ERS474308 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_6).  This submission includes reads tagged with the sequence TCTTCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474308">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474308</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581068</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362736</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_6#4" accession="ERX1416334" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416334</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_6#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_6#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362737, constructed from sample accession ERS474322 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_6).  This submission includes reads tagged with the sequence TGAAGAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474322">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474322</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581082</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362737</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_6#5" accession="ERX1416335" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416335</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_6#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_6#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362738, constructed from sample accession ERS474334 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_6).  This submission includes reads tagged with the sequence TGGAACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474334">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474334</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581094</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362738</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_6#6" accession="ERX1416336" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416336</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_6#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_6#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362739, constructed from sample accession ERS474342 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_6).  This submission includes reads tagged with the sequence TGGCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474342">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474342</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581102</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362739</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_6#7" accession="ERX1416337" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416337</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_6#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_6#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362740, constructed from sample accession ERS474352 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_6).  This submission includes reads tagged with the sequence TGGTGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474352">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581112</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362740</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_6#8" accession="ERX1416338" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416338</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_6#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_6#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362741, constructed from sample accession ERS474364 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_6).  This submission includes reads tagged with the sequence TTCACGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474364">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474364</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581124</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362741</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_6#9" accession="ERX1416339" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416339</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_6#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_6#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362742, constructed from sample accession ERS474373 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_6).  This submission includes reads tagged with the sequence AACTCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474373">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474373</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581133</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362742</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_6#10" accession="ERX1416340" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416340</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_6#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_6#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362743, constructed from sample accession ERS474387 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_6).  This submission includes reads tagged with the sequence AAGAGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474387">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474387</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581147</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362743</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_6#11" accession="ERX1416341" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416341</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_6#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_6#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362744, constructed from sample accession ERS474398 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_6).  This submission includes reads tagged with the sequence AAGGACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474398">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474398</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581158</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362744</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_6#12" accession="ERX1416342" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416342</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_6#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_6#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362745, constructed from sample accession ERS474420 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_6).  This submission includes reads tagged with the sequence AATCCGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474420">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474420</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581180</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362745</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_7#1" accession="ERX1416343" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416343</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_7#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_7#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362734, constructed from sample accession ERS474279 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_7).  This submission includes reads tagged with the sequence TATCAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474279">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474279</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581039</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362734</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_7#2" accession="ERX1416344" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416344</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_7#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_7#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362735, constructed from sample accession ERS474294 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_7).  This submission includes reads tagged with the sequence TCCGTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474294">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474294</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581054</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362735</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_7#3" accession="ERX1416345" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416345</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_7#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_7#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362736, constructed from sample accession ERS474308 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_7).  This submission includes reads tagged with the sequence TCTTCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474308">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474308</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581068</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362736</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_7#4" accession="ERX1416346" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416346</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_7#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_7#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362737, constructed from sample accession ERS474322 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_7).  This submission includes reads tagged with the sequence TGAAGAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474322">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474322</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581082</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362737</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_7#5" accession="ERX1416347" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416347</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_7#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_7#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362738, constructed from sample accession ERS474334 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_7).  This submission includes reads tagged with the sequence TGGAACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474334">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474334</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581094</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362738</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_7#6" accession="ERX1416348" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416348</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_7#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_7#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362739, constructed from sample accession ERS474342 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_7).  This submission includes reads tagged with the sequence TGGCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474342">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474342</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581102</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362739</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_7#7" accession="ERX1416349" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416349</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_7#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_7#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362740, constructed from sample accession ERS474352 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_7).  This submission includes reads tagged with the sequence TGGTGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474352">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581112</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362740</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_7#8" accession="ERX1416350" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416350</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_7#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_7#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362741, constructed from sample accession ERS474364 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_7).  This submission includes reads tagged with the sequence TTCACGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474364">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474364</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581124</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362741</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_7#9" accession="ERX1416351" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416351</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_7#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_7#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362742, constructed from sample accession ERS474373 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_7).  This submission includes reads tagged with the sequence AACTCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474373">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474373</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581133</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362742</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_7#10" accession="ERX1416352" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416352</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_7#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_7#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362743, constructed from sample accession ERS474387 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_7).  This submission includes reads tagged with the sequence AAGAGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474387">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474387</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581147</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362743</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_7#11" accession="ERX1416353" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416353</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_7#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_7#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362744, constructed from sample accession ERS474398 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_7).  This submission includes reads tagged with the sequence AAGGACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474398">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474398</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581158</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362744</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_7#12" accession="ERX1416354" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416354</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_7#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_7#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362745, constructed from sample accession ERS474420 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_7).  This submission includes reads tagged with the sequence AATCCGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474420">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474420</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581180</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362745</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_8#1" accession="ERX1416355" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416355</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_8#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_8#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362734, constructed from sample accession ERS474279 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_8).  This submission includes reads tagged with the sequence TATCAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474279">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474279</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581039</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362734</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_8#2" accession="ERX1416356" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416356</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_8#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_8#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362735, constructed from sample accession ERS474294 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_8).  This submission includes reads tagged with the sequence TCCGTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474294">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474294</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581054</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362735</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_8#3" accession="ERX1416357" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416357</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_8#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_8#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362736, constructed from sample accession ERS474308 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_8).  This submission includes reads tagged with the sequence TCTTCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474308">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474308</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581068</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362736</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_8#4" accession="ERX1416358" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416358</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_8#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_8#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362737, constructed from sample accession ERS474322 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_8).  This submission includes reads tagged with the sequence TGAAGAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474322">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474322</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581082</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362737</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_8#5" accession="ERX1416359" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416359</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_8#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_8#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362738, constructed from sample accession ERS474334 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_8).  This submission includes reads tagged with the sequence TGGAACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474334">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474334</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581094</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362738</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_8#6" accession="ERX1416360" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416360</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_8#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_8#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362739, constructed from sample accession ERS474342 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_8).  This submission includes reads tagged with the sequence TGGCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474342">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474342</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581102</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362739</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_8#7" accession="ERX1416361" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416361</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_8#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_8#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362740, constructed from sample accession ERS474352 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_8).  This submission includes reads tagged with the sequence TGGTGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474352">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581112</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362740</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_8#8" accession="ERX1416362" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416362</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_8#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_8#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362741, constructed from sample accession ERS474364 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_8).  This submission includes reads tagged with the sequence TTCACGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474364">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474364</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581124</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362741</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_8#9" accession="ERX1416363" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416363</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_8#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_8#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362742, constructed from sample accession ERS474373 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_8).  This submission includes reads tagged with the sequence AACTCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474373">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474373</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581133</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362742</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_8#10" accession="ERX1416364" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416364</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_8#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_8#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362743, constructed from sample accession ERS474387 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_8).  This submission includes reads tagged with the sequence AAGAGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474387">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474387</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581147</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362743</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_8#11" accession="ERX1416365" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416365</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_8#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_8#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362744, constructed from sample accession ERS474398 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_8).  This submission includes reads tagged with the sequence AAGGACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474398">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474398</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581158</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362744</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="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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18672_8#12" accession="ERX1416366" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1416366</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18672_8#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18672_8#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP006001">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006001</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15362745, constructed from sample accession ERS474420 for study accession ERP006001.  This is part of an Illumina multiplexed sequencing run (18672_8).  This submission includes reads tagged with the sequence AATCCGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS474420">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS474420</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2581180</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15362745</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="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_SET>
