<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="SC_EXP_4827_1#1" accession="ERX2009215">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2009215</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_4827_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_4827_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II sequencing</TITLE>
    <STUDY_REF accession="ERP000158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000158</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT203663A, constructed from sample accession ERS005861 for study accession ERP000158.  This is part of an Illumina multiplexed sequencing run (4827_1).  This submission includes reads tagged with the sequence ATCACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS005861">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS005861</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA969666</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT203663A</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </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_4827_1#2" accession="ERX2009216">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2009216</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_4827_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_4827_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II sequencing</TITLE>
    <STUDY_REF accession="ERP000158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000158</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT203664B, constructed from sample accession ERS005852 for study accession ERP000158.  This is part of an Illumina multiplexed sequencing run (4827_1).  This submission includes reads tagged with the sequence CGATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS005852">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS005852</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA969651</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT203664B</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </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_4827_1#3" accession="ERX2009217">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2009217</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_4827_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_4827_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II sequencing</TITLE>
    <STUDY_REF accession="ERP000158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000158</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT203665C, constructed from sample accession ERS005866 for study accession ERP000158.  This is part of an Illumina multiplexed sequencing run (4827_1).  This submission includes reads tagged with the sequence TTAGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS005866">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS005866</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA969658</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT203665C</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </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_4827_1#4" accession="ERX2009218">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2009218</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_4827_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_4827_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II sequencing</TITLE>
    <STUDY_REF accession="ERP000158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000158</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT203666D, constructed from sample accession ERS005855 for study accession ERP000158.  This is part of an Illumina multiplexed sequencing run (4827_1).  This submission includes reads tagged with the sequence TGACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS005855">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS005855</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA969626</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT203666D</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </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_4827_1#5" accession="ERX2009219">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2009219</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_4827_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_4827_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II sequencing</TITLE>
    <STUDY_REF accession="ERP000158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000158</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT203667E, constructed from sample accession ERS005856 for study accession ERP000158.  This is part of an Illumina multiplexed sequencing run (4827_1).  This submission includes reads tagged with the sequence ACAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS005856">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS005856</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA969638</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT203667E</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </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_4827_1#6" accession="ERX2009220">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2009220</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_4827_1#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_4827_1#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II sequencing</TITLE>
    <STUDY_REF accession="ERP000158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000158</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT203668F, constructed from sample accession ERS005858 for study accession ERP000158.  This is part of an Illumina multiplexed sequencing run (4827_1).  This submission includes reads tagged with the sequence GCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS005858">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS005858</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA969622</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT203668F</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </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_4827_1#7" accession="ERX2009221">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2009221</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_4827_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_4827_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II sequencing</TITLE>
    <STUDY_REF accession="ERP000158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000158</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT203669G, constructed from sample accession ERS005860 for study accession ERP000158.  This is part of an Illumina multiplexed sequencing run (4827_1).  This submission includes reads tagged with the sequence CAGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS005860">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS005860</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA969662</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT203669G</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </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_4827_1#8" accession="ERX2009222">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2009222</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_4827_1#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_4827_1#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II sequencing</TITLE>
    <STUDY_REF accession="ERP000158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000158</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT203670W, constructed from sample accession ERS005859 for study accession ERP000158.  This is part of an Illumina multiplexed sequencing run (4827_1).  This submission includes reads tagged with the sequence ACTTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS005859">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS005859</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA969619</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT203670W</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </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_4827_1#9" accession="ERX2009223">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2009223</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_4827_1#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_4827_1#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II sequencing</TITLE>
    <STUDY_REF accession="ERP000158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000158</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT203671A, constructed from sample accession ERS005870 for study accession ERP000158.  This is part of an Illumina multiplexed sequencing run (4827_1).  This submission includes reads tagged with the sequence GATCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS005870">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS005870</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA969615</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT203671A</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </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_4827_1#10" accession="ERX2009224">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2009224</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_4827_1#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_4827_1#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II sequencing</TITLE>
    <STUDY_REF accession="ERP000158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000158</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT203672B, constructed from sample accession ERS005862 for study accession ERP000158.  This is part of an Illumina multiplexed sequencing run (4827_1).  This submission includes reads tagged with the sequence TAGCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS005862">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS005862</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA969669</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT203672B</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </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_4827_1#11" accession="ERX2009225">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2009225</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_4827_1#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_4827_1#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II sequencing</TITLE>
    <STUDY_REF accession="ERP000158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000158</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT203673C, constructed from sample accession ERS005863 for study accession ERP000158.  This is part of an Illumina multiplexed sequencing run (4827_1).  This submission includes reads tagged with the sequence GGCTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS005863">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS005863</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA969672</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT203673C</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </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_4827_1#12" accession="ERX2009226">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2009226</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_4827_1#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_4827_1#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II sequencing</TITLE>
    <STUDY_REF accession="ERP000158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000158</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT203674D, constructed from sample accession ERS005864 for study accession ERP000158.  This is part of an Illumina multiplexed sequencing run (4827_1).  This submission includes reads tagged with the sequence CTTGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS005864">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS005864</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA969655</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT203674D</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </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>
