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      <SUBMITTER_ID namespace="SC">SC_EXP_5352_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5352_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000149">
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        <PRIMARY_ID>ERP000149</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT214085U, constructed from sample accession ERS012453 for study accession ERP000149.  This is part of an Illumina multiplexed sequencing run (5352_2).  This submission includes reads tagged with the sequence ATCACGTTAT.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>ERS012453</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA864178</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
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        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
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        </LIBRARY_LAYOUT>
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      </LIBRARY_DESCRIPTOR>
    </DESIGN>
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      </ILLUMINA>
    </PLATFORM>
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      <PRIMARY_ID>ERX2004541</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5352_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5352_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000149">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000149</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT214086V, constructed from sample accession ERS012454 for study accession ERP000149.  This is part of an Illumina multiplexed sequencing run (5352_2).  This submission includes reads tagged with the sequence CGATGTTTAT.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>ERS012454</PRIMARY_ID>
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        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
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        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
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        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="317" NOMINAL_SDEV="95"/>
        </LIBRARY_LAYOUT>
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        <INSTRUMENT_MODEL>Illumina Genome Analyzer II</INSTRUMENT_MODEL>
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      <PRIMARY_ID>ERX2004542</PRIMARY_ID>
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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5352_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000149">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000149</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT214087W, constructed from sample accession ERS012455 for study accession ERP000149.  This is part of an Illumina multiplexed sequencing run (5352_2).  This submission includes reads tagged with the sequence TTAGGCATAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS012455">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS012455</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA864164</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT214087W</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="305" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
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        <INSTRUMENT_MODEL>Illumina Genome Analyzer II</INSTRUMENT_MODEL>
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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5352_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000149">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000149</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT214088A, constructed from sample accession ERS012456 for study accession ERP000149.  This is part of an Illumina multiplexed sequencing run (5352_2).  This submission includes reads tagged with the sequence TGACCACTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS012456">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS012456</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA864167</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT214088A</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
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        <INSTRUMENT_MODEL>Illumina Genome Analyzer II</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <PRIMARY_ID>ERX2004544</PRIMARY_ID>
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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5352_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000149">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000149</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT214089B, constructed from sample accession ERS012457 for study accession ERP000149.  This is part of an Illumina multiplexed sequencing run (5352_2).  This submission includes reads tagged with the sequence ACAGTGGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS012457">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS012457</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA864142</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT214089B</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299" NOMINAL_SDEV="83"/>
        </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>
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    <IDENTIFIERS>
      <PRIMARY_ID>ERX2004545</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5352_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5352_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000149">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000149</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT214090R, constructed from sample accession ERS012458 for study accession ERP000149.  This is part of an Illumina multiplexed sequencing run (5352_2).  This submission includes reads tagged with the sequence GCCAATGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS012458">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS012458</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA864139</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT214090R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="332" 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>
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