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  <EXPERIMENT alias="SC_EXP_5740_4#1" accession="ERX1997387" broker_name="">
    <IDENTIFIERS>
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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5740_4#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000426">
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        <PRIMARY_ID>ERP000426</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT224987I, constructed from sample accession ERS018134 for study accession ERP000426.  This is part of an Illumina multiplexed sequencing run (5740_4).  This submission includes reads tagged with the sequence ATCACGTTAT.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>ERS018134</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA905975</EXTERNAL_ID>
        </IDENTIFIERS>
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        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="169" NOMINAL_SDEV="48"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5740_4#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000426">
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        <PRIMARY_ID>ERP000426</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT224988J, constructed from sample accession ERS018135 for study accession ERP000426.  This is part of an Illumina multiplexed sequencing run (5740_4).  This submission includes reads tagged with the sequence CGATGTTTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS018135">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS018135</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA905976</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT224988J</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="167" NOMINAL_SDEV="45"/>
        </LIBRARY_LAYOUT>
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