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    <IDENTIFIERS>
      <PRIMARY_ID>ERX2004290</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5731_6#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5731_6#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000287">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000287</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT224775V, constructed from sample accession ERS017782 for study accession ERP000287.  This is part of an Illumina multiplexed sequencing run (5731_6).  This submission includes reads tagged with the sequence ATCACGTTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS017782">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS017782</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA864317</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT224775V</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="281" NOMINAL_SDEV="78"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer II</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_5731_6#2" accession="ERX2004291">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2004291</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5731_6#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5731_6#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000287">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000287</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT224776W, constructed from sample accession ERS017783 for study accession ERP000287.  This is part of an Illumina multiplexed sequencing run (5731_6).  This submission includes reads tagged with the sequence CGATGTTTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS017783">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS017783</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA864318</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT224776W</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="274" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer II</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_5731_6#3" accession="ERX2004292">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2004292</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5731_6#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5731_6#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000287">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000287</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT224777A, constructed from sample accession ERS017784 for study accession ERP000287.  This is part of an Illumina multiplexed sequencing run (5731_6).  This submission includes reads tagged with the sequence TTAGGCATAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS017784">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS017784</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA864315</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT224777A</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="286" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer II</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_5731_6#4" accession="ERX2004293">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2004293</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5731_6#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5731_6#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000287">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000287</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT224778B, constructed from sample accession ERS017785 for study accession ERP000287.  This is part of an Illumina multiplexed sequencing run (5731_6).  This submission includes reads tagged with the sequence TGACCACTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS017785">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS017785</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA864316</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT224778B</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="275" NOMINAL_SDEV="73"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer II</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_5731_6#5" accession="ERX2004294">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2004294</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5731_6#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5731_6#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000287">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000287</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT224779C, constructed from sample accession ERS017779 for study accession ERP000287.  This is part of an Illumina multiplexed sequencing run (5731_6).  This submission includes reads tagged with the sequence ACAGTGGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS017779">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS017779</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA864258</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT224779C</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="283" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer II</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_5731_6#6" accession="ERX2004295">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2004295</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5731_6#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5731_6#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000287">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000287</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT224780S, constructed from sample accession ERS017787 for study accession ERP000287.  This is part of an Illumina multiplexed sequencing run (5731_6).  This submission includes reads tagged with the sequence GCCAATGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS017787">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS017787</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA864314</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT224780S</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="270" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer II</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_5731_6#7" accession="ERX2004296">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2004296</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5731_6#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5731_6#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000287">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000287</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT224781T, constructed from sample accession ERS017789 for study accession ERP000287.  This is part of an Illumina multiplexed sequencing run (5731_6).  This submission includes reads tagged with the sequence CAGATCTGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS017789">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS017789</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA864322</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT224781T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="270" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer II</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_5731_6#8" accession="ERX2004297">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2004297</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5731_6#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5731_6#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000287">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000287</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT224782U, constructed from sample accession ERS017790 for study accession ERP000287.  This is part of an Illumina multiplexed sequencing run (5731_6).  This submission includes reads tagged with the sequence ACTTGATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS017790">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS017790</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA864295</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT224782U</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="276" NOMINAL_SDEV="69"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer II</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_5731_6#9" accession="ERX2004298">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2004298</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5731_6#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5731_6#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000287">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000287</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT224783V, constructed from sample accession ERS017791 for study accession ERP000287.  This is part of an Illumina multiplexed sequencing run (5731_6).  This submission includes reads tagged with the sequence GATCAGCGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS017791">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS017791</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA864294</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT224783V</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="276" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer II</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_5731_6#10" accession="ERX2004299">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2004299</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5731_6#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5731_6#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000287">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000287</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT224784W, constructed from sample accession ERS017792 for study accession ERP000287.  This is part of an Illumina multiplexed sequencing run (5731_6).  This submission includes reads tagged with the sequence TAGCTTGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS017792">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS017792</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA864297</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT224784W</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="277" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer II</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_5731_6#11" accession="ERX2004300">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2004300</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5731_6#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5731_6#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000287">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000287</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT224785A, constructed from sample accession ERS017793 for study accession ERP000287.  This is part of an Illumina multiplexed sequencing run (5731_6).  This submission includes reads tagged with the sequence GGCTACAGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS017793">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS017793</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA864296</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT224785A</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="291" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer II</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_5731_6#12" accession="ERX2004301">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2004301</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5731_6#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5731_6#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000287">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000287</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT224786B, constructed from sample accession ERS017794 for study accession ERP000287.  This is part of an Illumina multiplexed sequencing run (5731_6).  This submission includes reads tagged with the sequence CTTGTACTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS017794">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS017794</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA864291</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT224786B</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="286" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer II</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
