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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5082_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
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        <PRIMARY_ID>ERP000110</PRIMARY_ID>
      </IDENTIFIERS>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT206804H, constructed from sample accession ERS009748 for study accession ERP000110.  This is part of an Illumina multiplexed sequencing run (5082_1).  This submission includes reads tagged with the sequence TTAGGCATAT.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>ERS009748</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA715551</EXTERNAL_ID>
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      </SAMPLE_DESCRIPTOR>
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        <LIBRARY_NAME>NT206804H</LIBRARY_NAME>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="90" NOMINAL_SDEV="3"/>
        </LIBRARY_LAYOUT>
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    </DESIGN>
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  <EXPERIMENT alias="SC_EXP_5082_1#4" accession="ERX2007177">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2007177</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5082_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5082_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000110">
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        <PRIMARY_ID>ERP000110</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT206805I, constructed from sample accession ERS009749 for study accession ERP000110.  This is part of an Illumina multiplexed sequencing run (5082_1).  This submission includes reads tagged with the sequence TGACCACTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS009749">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS009749</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA715314</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT206805I</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="90" NOMINAL_SDEV="1"/>
        </LIBRARY_LAYOUT>
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