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    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
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      <DESIGN_DESCRIPTION>Illumina sequencing of library NT29037M, constructed from sample accession ERS005246 for study accession ERP000139.  This is part of an Illumina multiplexed sequencing run (4311_7).  This submission includes reads tagged with the sequence ATCACG.</DESIGN_DESCRIPTION>
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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_4311_7#2</SUBMITTER_ID>
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    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
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      <DESIGN_DESCRIPTION>Illumina sequencing of library NT29037M, constructed from sample accession ERS005255 for study accession ERP000139.  This is part of an Illumina multiplexed sequencing run (4311_7).  This submission includes reads tagged with the sequence CGATGT.</DESIGN_DESCRIPTION>
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    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
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      <DESIGN_DESCRIPTION>Illumina sequencing of library NT29037M, constructed from sample accession ERS005254 for study accession ERP000139.  This is part of an Illumina multiplexed sequencing run (4311_7).  This submission includes reads tagged with the sequence TTAGGC.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>ERS005254</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA677624</EXTERNAL_ID>
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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_4311_7#4</SUBMITTER_ID>
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    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000139">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000139</PRIMARY_ID>
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    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT29037M, constructed from sample accession ERS005253 for study accession ERP000139.  This is part of an Illumina multiplexed sequencing run (4311_7).  This submission includes reads tagged with the sequence TGACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS005253">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS005253</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA677617</EXTERNAL_ID>
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        <LIBRARY_NAME>NT29037M</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_4311_7#5</SUBMITTER_ID>
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    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000139">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000139</PRIMARY_ID>
      </IDENTIFIERS>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT29037M, constructed from sample accession ERS005252 for study accession ERP000139.  This is part of an Illumina multiplexed sequencing run (4311_7).  This submission includes reads tagged with the sequence ACAGTG.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>ERS005252</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA677618</EXTERNAL_ID>
        </IDENTIFIERS>
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        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" NOMINAL_SDEV="62"/>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
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        <INSTRUMENT_MODEL>Illumina Genome Analyzer II</INSTRUMENT_MODEL>
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      <PRIMARY_ID>ERX2008129</PRIMARY_ID>
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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_4311_7#6</SUBMITTER_ID>
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    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000139">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000139</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT29037M, constructed from sample accession ERS005251 for study accession ERP000139.  This is part of an Illumina multiplexed sequencing run (4311_7).  This submission includes reads tagged with the sequence GCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS005251">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS005251</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA677619</EXTERNAL_ID>
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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_4311_7#7</SUBMITTER_ID>
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    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
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        <PRIMARY_ID>ERP000139</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>Illumina sequencing of library NT29037M, constructed from sample accession ERS005250 for study accession ERP000139.  This is part of an Illumina multiplexed sequencing run (4311_7).  This submission includes reads tagged with the sequence CAGATC.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>ERS005250</PRIMARY_ID>
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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_4311_7#8</SUBMITTER_ID>
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    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
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        <PRIMARY_ID>ERP000139</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>Illumina sequencing of library NT29037M, constructed from sample accession ERS005248 for study accession ERP000139.  This is part of an Illumina multiplexed sequencing run (4311_7).  This submission includes reads tagged with the sequence ACTTGA.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>ERS005248</PRIMARY_ID>
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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_4311_7#9</SUBMITTER_ID>
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    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
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        <PRIMARY_ID>ERP000139</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>Illumina sequencing of library NT29037M, constructed from sample accession ERS005249 for study accession ERP000139.  This is part of an Illumina multiplexed sequencing run (4311_7).  This submission includes reads tagged with the sequence GATCAG.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>ERS005249</PRIMARY_ID>
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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_4311_7#10</SUBMITTER_ID>
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    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
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        <PRIMARY_ID>ERP000139</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT29037M, constructed from sample accession ERS005247 for study accession ERP000139.  This is part of an Illumina multiplexed sequencing run (4311_7).  This submission includes reads tagged with the sequence TAGCTT.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>ERS005247</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA677665</EXTERNAL_ID>
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        <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_4311_7#11</SUBMITTER_ID>
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    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
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        <PRIMARY_ID>ERP000139</PRIMARY_ID>
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    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT29037M, constructed from sample accession ERS005245 for study accession ERP000139.  This is part of an Illumina multiplexed sequencing run (4311_7).  This submission includes reads tagged with the sequence GGCTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS005245">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS005245</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA677663</EXTERNAL_ID>
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        <LIBRARY_NAME>NT29037M</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="214" NOMINAL_SDEV="61"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer II</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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      <PRIMARY_ID>ERX2008135</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_4311_7#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_4311_7#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000139">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000139</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT29037M, constructed from sample accession ERS005257 for study accession ERP000139.  This is part of an Illumina multiplexed sequencing run (4311_7).  This submission includes reads tagged with the sequence CTTGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS005257">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS005257</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA677621</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT29037M</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
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        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer II</INSTRUMENT_MODEL>
      </ILLUMINA>
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