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  <EXPERIMENT alias="SC_EXP_5103_7#1" accession="ERX2006699">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2006699</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5103_7#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5103_7#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000170">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000170</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT207371H, constructed from sample accession ERS008580 for study accession ERP000170.  This is part of an Illumina multiplexed sequencing run (5103_7).  This submission includes reads tagged with the sequence ATCACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS008580">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS008580</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA980171</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT207371H</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="235" NOMINAL_SDEV="58"/>
        </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_5103_7#2" accession="ERX2006700">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2006700</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5103_7#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5103_7#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000170">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000170</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT207372I, constructed from sample accession ERS008581 for study accession ERP000170.  This is part of an Illumina multiplexed sequencing run (5103_7).  This submission includes reads tagged with the sequence CGATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS008581">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS008581</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA980172</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT207372I</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="269" 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_5103_7#3" accession="ERX2006701">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2006701</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5103_7#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5103_7#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000170">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000170</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT207373J, constructed from sample accession ERS008582 for study accession ERP000170.  This is part of an Illumina multiplexed sequencing run (5103_7).  This submission includes reads tagged with the sequence TTAGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS008582">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS008582</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA980173</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT207373J</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="252" NOMINAL_SDEV="64"/>
        </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_5103_7#4" accession="ERX2006702">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2006702</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5103_7#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5103_7#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000170">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000170</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT207374K, constructed from sample accession ERS008583 for study accession ERP000170.  This is part of an Illumina multiplexed sequencing run (5103_7).  This submission includes reads tagged with the sequence TGACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS008583">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS008583</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA980174</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT207374K</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="72"/>
        </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_5103_7#5" accession="ERX2006703">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2006703</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5103_7#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5103_7#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000170">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000170</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT207375L, constructed from sample accession ERS008584 for study accession ERP000170.  This is part of an Illumina multiplexed sequencing run (5103_7).  This submission includes reads tagged with the sequence ACAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS008584">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS008584</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA980175</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT207375L</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="248" NOMINAL_SDEV="71"/>
        </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_5103_7#6" accession="ERX2006704">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2006704</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5103_7#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5103_7#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000170">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000170</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT207376M, constructed from sample accession ERS008585 for study accession ERP000170.  This is part of an Illumina multiplexed sequencing run (5103_7).  This submission includes reads tagged with the sequence GCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS008585">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS008585</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA980176</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT207376M</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="262" 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_5103_7#7" accession="ERX2006705">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2006705</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5103_7#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5103_7#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000170">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000170</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT207377N, constructed from sample accession ERS008586 for study accession ERP000170.  This is part of an Illumina multiplexed sequencing run (5103_7).  This submission includes reads tagged with the sequence CAGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS008586">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS008586</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA980177</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT207377N</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="255" NOMINAL_SDEV="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_5103_7#8" accession="ERX2006706">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2006706</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5103_7#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5103_7#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000170">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000170</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT207378O, constructed from sample accession ERS008587 for study accession ERP000170.  This is part of an Illumina multiplexed sequencing run (5103_7).  This submission includes reads tagged with the sequence ACTTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS008587">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS008587</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA980178</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT207378O</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="265" 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_5103_7#9" accession="ERX2006707">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2006707</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5103_7#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5103_7#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000170">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000170</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT207379P, constructed from sample accession ERS008588 for study accession ERP000170.  This is part of an Illumina multiplexed sequencing run (5103_7).  This submission includes reads tagged with the sequence GATCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS008588">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS008588</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA980179</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT207379P</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="249" NOMINAL_SDEV="68"/>
        </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_5103_7#10" accession="ERX2006708">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2006708</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5103_7#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5103_7#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000170">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000170</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT207380I, constructed from sample accession ERS008589 for study accession ERP000170.  This is part of an Illumina multiplexed sequencing run (5103_7).  This submission includes reads tagged with the sequence TAGCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS008589">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS008589</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA980180</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT207380I</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260" 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_5103_7#11" accession="ERX2006709">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2006709</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5103_7#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5103_7#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000170">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000170</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT207381J, constructed from sample accession ERS008590 for study accession ERP000170.  This is part of an Illumina multiplexed sequencing run (5103_7).  This submission includes reads tagged with the sequence GGCTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS008590">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS008590</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA980169</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT207381J</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="244" NOMINAL_SDEV="66"/>
        </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_5103_7#12" accession="ERX2006710">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2006710</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5103_7#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5103_7#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000170">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000170</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT207382K, constructed from sample accession ERS008591 for study accession ERP000170.  This is part of an Illumina multiplexed sequencing run (5103_7).  This submission includes reads tagged with the sequence CTTGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS008591">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS008591</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA980168</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT207382K</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="79"/>
        </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>
