<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="SC_EXP_5159_7#1" accession="ERX2005227">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2005227</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5159_7#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5159_7#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000246">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000246</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT211909A, constructed from sample accession ERS011584 for study accession ERP000246.  This is part of an Illumina multiplexed sequencing run (5159_7).  This submission includes reads tagged with the sequence ATCACGTTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS011584">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS011584</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA970265</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT211909A</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="254" 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_5159_7#2" accession="ERX2005228">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2005228</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5159_7#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5159_7#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000246">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000246</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT211910Q, constructed from sample accession ERS011585 for study accession ERP000246.  This is part of an Illumina multiplexed sequencing run (5159_7).  This submission includes reads tagged with the sequence CGATGTTTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS011585">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS011585</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA970267</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT211910Q</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_5159_7#3" accession="ERX2005229">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2005229</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5159_7#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5159_7#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000246">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000246</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT211911R, constructed from sample accession ERS011586 for study accession ERP000246.  This is part of an Illumina multiplexed sequencing run (5159_7).  This submission includes reads tagged with the sequence TTAGGCATAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS011586">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS011586</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA970261</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT211911R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="236" NOMINAL_SDEV="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_5159_7#4" accession="ERX2005230">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2005230</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5159_7#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5159_7#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000246">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000246</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT211912S, constructed from sample accession ERS011587 for study accession ERP000246.  This is part of an Illumina multiplexed sequencing run (5159_7).  This submission includes reads tagged with the sequence TGACCACTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS011587">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS011587</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA970263</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT211912S</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="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_5159_7#5" accession="ERX2005231">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2005231</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5159_7#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5159_7#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000246">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000246</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT211913T, constructed from sample accession ERS011588 for study accession ERP000246.  This is part of an Illumina multiplexed sequencing run (5159_7).  This submission includes reads tagged with the sequence ACAGTGGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS011588">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS011588</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA970274</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT211913T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250" 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_5159_7#6" accession="ERX2005232">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2005232</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5159_7#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5159_7#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000246">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000246</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT211914U, constructed from sample accession ERS011589 for study accession ERP000246.  This is part of an Illumina multiplexed sequencing run (5159_7).  This submission includes reads tagged with the sequence GCCAATGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS011589">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS011589</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA970275</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT211914U</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="254" 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_5159_7#7" accession="ERX2005233">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2005233</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5159_7#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5159_7#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000246">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000246</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT211915V, constructed from sample accession ERS011590 for study accession ERP000246.  This is part of an Illumina multiplexed sequencing run (5159_7).  This submission includes reads tagged with the sequence CAGATCTGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS011590">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS011590</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA970205</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT211915V</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="253" 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_5159_7#8" accession="ERX2005234">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2005234</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5159_7#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5159_7#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000246">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000246</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT211916W, constructed from sample accession ERS011591 for study accession ERP000246.  This is part of an Illumina multiplexed sequencing run (5159_7).  This submission includes reads tagged with the sequence ACTTGATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS011591">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS011591</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA970204</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT211916W</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="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_5159_7#9" accession="ERX2005235">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2005235</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5159_7#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5159_7#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000246">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000246</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT211917A, constructed from sample accession ERS011592 for study accession ERP000246.  This is part of an Illumina multiplexed sequencing run (5159_7).  This submission includes reads tagged with the sequence GATCAGCGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS011592">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS011592</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA970207</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT211917A</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="246" NOMINAL_SDEV="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_5159_7#10" accession="ERX2005236">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2005236</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5159_7#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5159_7#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000246">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000246</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT211918B, constructed from sample accession ERS011593 for study accession ERP000246.  This is part of an Illumina multiplexed sequencing run (5159_7).  This submission includes reads tagged with the sequence TAGCTTGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS011593">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS011593</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA970206</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT211918B</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="67"/>
        </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_5159_7#11" accession="ERX2005237">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2005237</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5159_7#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5159_7#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000246">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000246</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT211919C, constructed from sample accession ERS011594 for study accession ERP000246.  This is part of an Illumina multiplexed sequencing run (5159_7).  This submission includes reads tagged with the sequence GGCTACAGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS011594">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS011594</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA970277</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT211919C</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="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_SET>
