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    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
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      </IDENTIFIERS>
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      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:A1, constructed from sample accession ERS1306209 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:B1, constructed from sample accession ERS1306210 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>ERS1306210</PRIMARY_ID>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:C1, constructed from sample accession ERS1306211 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306211</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394762</EXTERNAL_ID>
        </IDENTIFIERS>
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        <LIBRARY_NAME>DN462206K:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
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        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
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        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <PRIMARY_ID>ERX1830459</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:D1, constructed from sample accession ERS1306212 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306212</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394763</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:D1</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>
      </LIBRARY_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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      <PRIMARY_ID>ERX1830460</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:E1, constructed from sample accession ERS1306213 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306213</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394764</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830461</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:F1, constructed from sample accession ERS1306214 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306214</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394765</EXTERNAL_ID>
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        <LIBRARY_NAME>DN462206K:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
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        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="464" NOMINAL_SDEV="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#8</SUBMITTER_ID>
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    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:H1, constructed from sample accession ERS1306216 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306216</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394767</EXTERNAL_ID>
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        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
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        <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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <PRIMARY_ID>ERX1830463</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#9</SUBMITTER_ID>
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    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:A2, constructed from sample accession ERS1306217 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306217</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394768</EXTERNAL_ID>
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        <LIBRARY_NAME>DN462206K:A2</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 HiSeq 2500</INSTRUMENT_MODEL>
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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:B2, constructed from sample accession ERS1306218 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306218</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394769</EXTERNAL_ID>
        </IDENTIFIERS>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:B2</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>
      </LIBRARY_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:C2, constructed from sample accession ERS1306219 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306219</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394770</EXTERNAL_ID>
        </IDENTIFIERS>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="474" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#12" accession="ERX1830466" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830466</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:D2, constructed from sample accession ERS1306220 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306220">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306220</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394771</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="437" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#13" accession="ERX1830467" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830467</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:E2, constructed from sample accession ERS1306221 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306221">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306221</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394772</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#14" accession="ERX1830468" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830468</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:F2, constructed from sample accession ERS1306222 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306222">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306222</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394773</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="454" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#15" accession="ERX1830469" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830469</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:G2, constructed from sample accession ERS1306223 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306223">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306223</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394774</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="481" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#16" accession="ERX1830470" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830470</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:H2, constructed from sample accession ERS1306224 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306224">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306224</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394775</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="455" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#17" accession="ERX1830471" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830471</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:A3, constructed from sample accession ERS1306225 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306225">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306225</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394776</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#18" accession="ERX1830472" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830472</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:B3, constructed from sample accession ERS1306226 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306226">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306226</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394777</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="481" NOMINAL_SDEV="78"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#19" accession="ERX1830473" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830473</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:C3, constructed from sample accession ERS1306227 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306227">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306227</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394778</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="457" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#20" accession="ERX1830474" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830474</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:D3, constructed from sample accession ERS1306228 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306228">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306228</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394779</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="463" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#21" accession="ERX1830475" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830475</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:E3, constructed from sample accession ERS1306229 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306229">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306229</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394780</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="458" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#22" accession="ERX1830476" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830476</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:F3, constructed from sample accession ERS1306230 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306230">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306230</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394781</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="462" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#23" accession="ERX1830477" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830477</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:G3, constructed from sample accession ERS1306231 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306231">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306231</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394782</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#24" accession="ERX1830478" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830478</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:H3, constructed from sample accession ERS1306232 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306232">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306232</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394783</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="463" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#25" accession="ERX1830479" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830479</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:A4, constructed from sample accession ERS1306233 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306233">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306233</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394784</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="457" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#26" accession="ERX1830480" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830480</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:B4, constructed from sample accession ERS1306234 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306234">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306234</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394785</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#27" accession="ERX1830481" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830481</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:C4, constructed from sample accession ERS1306235 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306235">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306235</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394786</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="460" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#29" accession="ERX1830482" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830482</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:E4, constructed from sample accession ERS1306237 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306237">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306237</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394788</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#30" accession="ERX1830483" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830483</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:F4, constructed from sample accession ERS1306238 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306238">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306238</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394789</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="458" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#31" accession="ERX1830484" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830484</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:G4, constructed from sample accession ERS1306239 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306239">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306239</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394790</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#33" accession="ERX1830485" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830485</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:A5, constructed from sample accession ERS1306241 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306241">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306241</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394792</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="454" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#34" accession="ERX1830486" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830486</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:B5, constructed from sample accession ERS1306242 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306242">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306242</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394793</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="453" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#35" accession="ERX1830487" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830487</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:C5, constructed from sample accession ERS1306243 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306243">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306243</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394794</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#36" accession="ERX1830488" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830488</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:D5, constructed from sample accession ERS1306244 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306244">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306244</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394795</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#37" accession="ERX1830489" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830489</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:E5, constructed from sample accession ERS1306245 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306245">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306245</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394796</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="78"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#38" accession="ERX1830490" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830490</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:F5, constructed from sample accession ERS1306246 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306246">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306246</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394797</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="446" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#39" accession="ERX1830491" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830491</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#39</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:G5, constructed from sample accession ERS1306247 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306247">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306247</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394798</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#40" accession="ERX1830492" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830492</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#40</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:H5, constructed from sample accession ERS1306248 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306248">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306248</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394799</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="438" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#41" accession="ERX1830493" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830493</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#41</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:A6, constructed from sample accession ERS1306249 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306249">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306249</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394800</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="453" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#42" accession="ERX1830494" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830494</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#42</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:B6, constructed from sample accession ERS1306250 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306250">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306250</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394801</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="463" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#43" accession="ERX1830495" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830495</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#43</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:C6, constructed from sample accession ERS1306251 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306251">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306251</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394802</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="457" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#45" accession="ERX1830496" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830496</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#45</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:E6, constructed from sample accession ERS1306253 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306253">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306253</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394804</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#46" accession="ERX1830497" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830497</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#46</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:F6, constructed from sample accession ERS1306254 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306254">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306254</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394805</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="451" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#47" accession="ERX1830498" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830498</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#47</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:G6, constructed from sample accession ERS1306255 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306255">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306255</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394806</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="447" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#48" accession="ERX1830499" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830499</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#48</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:H6, constructed from sample accession ERS1306256 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306256">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306256</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394807</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="438" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#49" accession="ERX1830500" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830500</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#49</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:A7, constructed from sample accession ERS1306257 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306257">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306257</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394808</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:A7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="454" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#50" accession="ERX1830501" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830501</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#50</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:B7, constructed from sample accession ERS1306258 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306258">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306258</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394809</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="461" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#51" accession="ERX1830502" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830502</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#51</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:C7, constructed from sample accession ERS1306259 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306259">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306259</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394810</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="456" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#52" accession="ERX1830503" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830503</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#52</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:D7, constructed from sample accession ERS1306260 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306260">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306260</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394811</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="442" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#53" accession="ERX1830504" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830504</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#53</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:E7, constructed from sample accession ERS1306261 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306261">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306261</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394812</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#54" accession="ERX1830505" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830505</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#54</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:F7, constructed from sample accession ERS1306262 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306262">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306262</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394813</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="473" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#55" accession="ERX1830506" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830506</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#55</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:G7, constructed from sample accession ERS1306263 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306263">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306263</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394814</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#56" accession="ERX1830507" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830507</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#56</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:H7, constructed from sample accession ERS1306264 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306264">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306264</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394815</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="431" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#57" accession="ERX1830508" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830508</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#57</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:A8, constructed from sample accession ERS1306265 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306265">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306265</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394816</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="463" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#58" accession="ERX1830509" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830509</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#58</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:B8, constructed from sample accession ERS1306266 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306266">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306266</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394817</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:B8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="457" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#59" accession="ERX1830510" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830510</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#59</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:C8, constructed from sample accession ERS1306267 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306267">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306267</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394818</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#60" accession="ERX1830511" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830511</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#60</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#60</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:D8, constructed from sample accession ERS1306268 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306268">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306268</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394819</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:D8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="451" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#61" accession="ERX1830512" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830512</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#61</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:E8, constructed from sample accession ERS1306269 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306269">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306269</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394820</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="433" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#62" accession="ERX1830513" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830513</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#62</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:F8, constructed from sample accession ERS1306270 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306270">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306270</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394821</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#63" accession="ERX1830514" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830514</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#63</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#63</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:G8, constructed from sample accession ERS1306271 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306271">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306271</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394822</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="442" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#64" accession="ERX1830515" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830515</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#64</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#64</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:H8, constructed from sample accession ERS1306272 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306272">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306272</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394823</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:H8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="443" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#65" accession="ERX1830516" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830516</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#65</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#65</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:A9, constructed from sample accession ERS1306273 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306273">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306273</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394824</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:A9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="456" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#66" accession="ERX1830517" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830517</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#66</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#66</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:B9, constructed from sample accession ERS1306274 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306274">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306274</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394825</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:B9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="463" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#67" accession="ERX1830518" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830518</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#67</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:C9, constructed from sample accession ERS1306275 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306275">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306275</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394826</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:C9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#68" accession="ERX1830519" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830519</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#68</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:D9, constructed from sample accession ERS1306276 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306276">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306276</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394827</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#69" accession="ERX1830520" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830520</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#69</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#69</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:E9, constructed from sample accession ERS1306277 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306277">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306277</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394828</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:E9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#71" accession="ERX1830521" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830521</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#71</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#71</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:G9, constructed from sample accession ERS1306279 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GTGTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306279">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306279</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394830</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:G9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="436" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#72" accession="ERX1830522" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830522</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#72</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#72</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:H9, constructed from sample accession ERS1306280 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GACGGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306280">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306280</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394831</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:H9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="485" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#73" accession="ERX1830523" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830523</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#73</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#73</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:A10, constructed from sample accession ERS1306281 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306281">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306281</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394832</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:A10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#74" accession="ERX1830524" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830524</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#74</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:B10, constructed from sample accession ERS1306282 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306282">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306282</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394833</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:B10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="447" NOMINAL_SDEV="78"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#75" accession="ERX1830525" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830525</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#75</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:C10, constructed from sample accession ERS1306283 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GAATCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306283">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306283</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394834</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:C10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="456" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#76" accession="ERX1830526" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830526</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#76</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:D10, constructed from sample accession ERS1306284 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306284">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306284</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394835</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:D10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="78"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#77" accession="ERX1830527" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830527</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#77</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:E10, constructed from sample accession ERS1306285 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306285">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306285</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394836</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:E10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="438" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#80" accession="ERX1830528" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830528</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#80</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:H10, constructed from sample accession ERS1306288 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GTCGCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306288">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306288</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394839</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:H10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#81" accession="ERX1830529" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830529</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#81</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:A11, constructed from sample accession ERS1306289 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306289">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306289</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394840</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:A11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="467" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#82" accession="ERX1830530" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830530</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#82</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#82</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:B11, constructed from sample accession ERS1306290 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306290">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306290</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394841</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:B11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="456" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#84" accession="ERX1830531" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830531</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#84</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#84</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:D11, constructed from sample accession ERS1306292 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GTAAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306292">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306292</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394843</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:D11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#85" accession="ERX1830532" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830532</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#85</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#85</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:E11, constructed from sample accession ERS1306293 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GAGGATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306293">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306293</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394844</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:E11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#86" accession="ERX1830533" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830533</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#86</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:F11, constructed from sample accession ERS1306294 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GTTGTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306294">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306294</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394845</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:F11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="438" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#87" accession="ERX1830534" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830534</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#87</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:G11, constructed from sample accession ERS1306295 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GGATTAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306295">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306295</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394846</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:G11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#88" accession="ERX1830535" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830535</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#88</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#88</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:H11, constructed from sample accession ERS1306296 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GATAGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306296">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306296</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394847</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:H11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="416" NOMINAL_SDEV="66"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#89" accession="ERX1830536" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830536</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#89</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#89</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:A12, constructed from sample accession ERS1306297 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GTGTGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306297">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306297</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394848</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:A12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#90" accession="ERX1830537" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830537</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#90</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#90</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462206K:B12, constructed from sample accession ERS1306298 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GCAATCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306298">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306298</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394849</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462206K:B12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#91" accession="ERX1830538" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830538</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#91</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#91</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:A1, constructed from sample accession ERS1306299 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306299">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306299</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394850</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="455" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#92" accession="ERX1830539" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830539</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#92</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#92</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:B1, constructed from sample accession ERS1306300 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306300">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306300</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394851</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#93" accession="ERX1830540" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830540</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#93</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#93</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:C1, constructed from sample accession ERS1306301 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306301">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306301</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394852</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="463" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#94" accession="ERX1830541" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830541</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#94</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#94</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:D1, constructed from sample accession ERS1306302 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306302">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306302</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394853</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="446" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#95" accession="ERX1830542" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830542</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#95</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#95</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:E1, constructed from sample accession ERS1306303 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306303">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306303</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394854</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#96" accession="ERX1830543" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830543</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#96</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#96</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:F1, constructed from sample accession ERS1306304 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306304">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394855</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="442" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#97" accession="ERX1830544" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830544</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#97</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#97</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:G1, constructed from sample accession ERS1306305 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306305">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306305</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394856</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="461" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#98" accession="ERX1830545" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830545</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#98</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#98</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:H1, constructed from sample accession ERS1306306 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306306">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306306</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394857</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="429" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#99" accession="ERX1830546" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830546</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#99</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#99</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:A2, constructed from sample accession ERS1306307 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306307">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306307</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394858</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="464" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#100" accession="ERX1830547" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830547</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#100</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:B2, constructed from sample accession ERS1306308 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306308">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306308</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394859</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="479" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#102" accession="ERX1830548" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830548</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#102</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#102</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:D2, constructed from sample accession ERS1306310 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306310">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306310</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394861</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="471" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#103" accession="ERX1830549" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830549</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#103</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#103</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:E2, constructed from sample accession ERS1306311 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306311">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306311</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394862</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#104" accession="ERX1830550" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830550</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#104</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#104</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:F2, constructed from sample accession ERS1306312 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306312">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306312</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394863</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#105" accession="ERX1830551" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830551</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#105</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#105</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:G2, constructed from sample accession ERS1306313 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306313">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306313</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394864</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="451" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#106" accession="ERX1830552" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830552</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#106</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#106</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:H2, constructed from sample accession ERS1306314 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306314">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306314</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394865</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="435" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#107" accession="ERX1830553" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830553</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#107</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#107</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:A3, constructed from sample accession ERS1306315 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306315">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306315</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394866</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="465" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#108" accession="ERX1830554" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830554</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#108</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#108</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:B3, constructed from sample accession ERS1306316 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306316">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306316</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394867</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="464" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#109" accession="ERX1830555" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830555</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#109</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#109</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:C3, constructed from sample accession ERS1306317 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306317">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306317</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394868</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="471" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#110" accession="ERX1830556" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830556</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#110</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#110</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:D3, constructed from sample accession ERS1306318 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306318">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306318</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394869</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="472" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#111" accession="ERX1830557" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830557</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#111</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#111</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:E3, constructed from sample accession ERS1306319 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306319">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306319</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394870</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="481" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#112" accession="ERX1830558" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830558</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#112</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#112</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:F3, constructed from sample accession ERS1306320 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306320">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306320</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394871</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="458" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#113" accession="ERX1830559" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830559</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#113</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#113</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:G3, constructed from sample accession ERS1306321 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306321">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306321</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394872</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#114" accession="ERX1830560" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830560</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#114</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#114</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:H3, constructed from sample accession ERS1306322 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306322">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306322</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394873</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#115" accession="ERX1830561" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830561</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#115</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#115</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:A4, constructed from sample accession ERS1306323 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306323">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306323</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394874</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="442" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#116" accession="ERX1830562" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830562</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#116</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#116</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:B4, constructed from sample accession ERS1306324 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306324">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306324</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394875</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="443" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#117" accession="ERX1830563" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830563</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#117</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#117</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:C4, constructed from sample accession ERS1306325 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306325">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306325</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394876</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="465" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#118" accession="ERX1830564" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830564</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#118</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#118</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:D4, constructed from sample accession ERS1306326 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306326">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306326</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394877</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="460" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#120" accession="ERX1830565" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830565</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#120</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#120</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:F4, constructed from sample accession ERS1306328 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306328">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306328</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394879</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#122" accession="ERX1830566" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830566</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#122</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#122</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:H4, constructed from sample accession ERS1306330 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306330">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306330</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394881</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#123" accession="ERX1830567" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830567</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#123</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#123</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:A5, constructed from sample accession ERS1306331 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306331">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306331</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394882</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="460" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#124" accession="ERX1830568" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830568</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#124</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#124</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:B5, constructed from sample accession ERS1306332 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306332">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306332</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394883</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="458" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#125" accession="ERX1830569" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830569</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#125</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#125</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:C5, constructed from sample accession ERS1306333 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306333">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306333</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394884</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="461" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#126" accession="ERX1830570" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830570</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#126</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#126</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:D5, constructed from sample accession ERS1306334 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306334">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306334</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394885</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="447" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#127" accession="ERX1830571" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830571</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#127</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#127</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:E5, constructed from sample accession ERS1306335 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306335">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306335</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394886</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="439" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#128" accession="ERX1830572" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830572</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#128</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#128</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:F5, constructed from sample accession ERS1306336 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306336">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306336</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394887</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#129" accession="ERX1830573" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830573</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#129</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#129</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:G5, constructed from sample accession ERS1306337 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306337">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306337</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394888</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="462" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#130" accession="ERX1830574" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830574</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#130</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#130</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:H5, constructed from sample accession ERS1306338 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306338">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306338</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394889</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="447" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#131" accession="ERX1830575" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830575</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#131</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#131</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:A6, constructed from sample accession ERS1306339 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306339">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306339</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394890</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="454" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#132" accession="ERX1830576" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830576</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#132</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#132</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:B6, constructed from sample accession ERS1306340 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306340">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306340</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394891</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="453" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#133" accession="ERX1830577" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830577</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#133</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#133</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:C6, constructed from sample accession ERS1306341 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306341">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306341</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394892</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="456" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#134" accession="ERX1830578" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830578</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#134</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#134</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:D6, constructed from sample accession ERS1306342 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306342">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306342</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394893</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="455" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#136" accession="ERX1830579" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830579</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#136</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#136</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:F6, constructed from sample accession ERS1306344 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306344">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306344</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394895</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#137" accession="ERX1830580" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830580</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#137</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#137</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:G6, constructed from sample accession ERS1306345 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306345">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306345</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394896</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="472" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#138" accession="ERX1830581" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830581</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#138</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#138</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:H6, constructed from sample accession ERS1306346 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306346">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306346</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394897</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="443" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#139" accession="ERX1830582" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830582</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#139</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#139</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:A7, constructed from sample accession ERS1306347 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306347">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394898</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:A7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#140" accession="ERX1830583" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830583</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#140</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#140</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:B7, constructed from sample accession ERS1306348 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306348">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394899</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="457" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#141" accession="ERX1830584" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830584</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#141</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#141</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:C7, constructed from sample accession ERS1306349 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306349">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306349</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394900</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#142" accession="ERX1830585" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830585</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#142</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#142</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:D7, constructed from sample accession ERS1306350 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306350">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306350</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394901</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#143" accession="ERX1830586" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830586</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#143</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#143</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:E7, constructed from sample accession ERS1306351 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306351">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394902</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#144" accession="ERX1830587" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830587</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#144</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#144</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:F7, constructed from sample accession ERS1306352 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306352">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394903</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="443" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#145" accession="ERX1830588" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830588</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#145</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#145</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:G7, constructed from sample accession ERS1306353 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306353">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306353</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394904</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="442" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#146" accession="ERX1830589" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830589</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#146</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#146</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:H7, constructed from sample accession ERS1306354 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306354">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306354</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394905</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="458" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#147" accession="ERX1830590" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830590</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#147</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#147</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:A8, constructed from sample accession ERS1306355 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306355">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306355</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394906</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="451" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#148" accession="ERX1830591" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830591</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#148</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#148</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:B8, constructed from sample accession ERS1306356 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306356">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306356</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394907</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:B8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#149" accession="ERX1830592" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830592</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#149</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#149</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:C8, constructed from sample accession ERS1306357 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306357">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306357</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394908</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="463" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#150" accession="ERX1830593" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830593</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#150</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#150</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:D8, constructed from sample accession ERS1306358 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306358">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306358</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394909</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:D8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="447" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#152" accession="ERX1830594" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830594</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#152</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#152</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:F8, constructed from sample accession ERS1306360 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306360">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306360</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394911</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="442" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#153" accession="ERX1830595" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830595</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#153</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#153</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:G8, constructed from sample accession ERS1306361 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306361">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306361</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394912</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#154" accession="ERX1830596" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830596</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#154</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#154</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:H8, constructed from sample accession ERS1306362 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306362">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306362</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394913</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:H8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="454" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#155" accession="ERX1830597" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830597</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#155</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#155</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:A9, constructed from sample accession ERS1306363 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306363">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306363</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394914</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:A9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#156" accession="ERX1830598" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830598</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#156</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#156</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:B9, constructed from sample accession ERS1306364 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306364">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306364</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394915</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:B9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#157" accession="ERX1830599" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830599</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#157</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#157</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:C9, constructed from sample accession ERS1306365 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306365">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306365</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394916</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:C9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="447" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#158" accession="ERX1830600" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830600</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#158</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#158</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:D9, constructed from sample accession ERS1306366 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306366">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306366</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394917</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="454" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#159" accession="ERX1830601" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830601</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#159</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#159</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:E9, constructed from sample accession ERS1306367 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306367">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306367</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394918</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:E9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#160" accession="ERX1830602" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830602</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#160</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#160</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:F9, constructed from sample accession ERS1306368 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306368">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306368</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394919</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:F9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="469" NOMINAL_SDEV="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#161" accession="ERX1830603" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830603</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#161</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#161</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:G9, constructed from sample accession ERS1306369 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GTGTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306369">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306369</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394920</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:G9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="447" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#162" accession="ERX1830604" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830604</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#162</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#162</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:H9, constructed from sample accession ERS1306370 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GACGGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306370">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306370</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394921</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:H9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" NOMINAL_SDEV="74"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#163" accession="ERX1830605" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830605</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#163</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#163</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:A10, constructed from sample accession ERS1306371 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306371">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306371</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394922</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:A10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="455" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#164" accession="ERX1830606" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830606</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#164</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#164</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:B10, constructed from sample accession ERS1306372 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306372">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306372</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394923</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:B10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#165" accession="ERX1830607" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830607</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#165</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#165</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:C10, constructed from sample accession ERS1306373 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GAATCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306373">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306373</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394924</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:C10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="456" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#166" accession="ERX1830608" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830608</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#166</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#166</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:D10, constructed from sample accession ERS1306374 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306374">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306374</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394925</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:D10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="438" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#167" accession="ERX1830609" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830609</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#167</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#167</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:E10, constructed from sample accession ERS1306375 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306375">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306375</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394926</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:E10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="437" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#168" accession="ERX1830610" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830610</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#168</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#168</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:F10, constructed from sample accession ERS1306376 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306376">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306376</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394927</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:F10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="434" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#169" accession="ERX1830611" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830611</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#169</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#169</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:G10, constructed from sample accession ERS1306377 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306377">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306377</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394928</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:G10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="460" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#170" accession="ERX1830612" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830612</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#170</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#170</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:H10, constructed from sample accession ERS1306378 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GTCGCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306378">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306378</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394929</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:H10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#171" accession="ERX1830613" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830613</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#171</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#171</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:A11, constructed from sample accession ERS1306379 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306379">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306379</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394930</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:A11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="438" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#172" accession="ERX1830614" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830614</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#172</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#172</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:B11, constructed from sample accession ERS1306380 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306380">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306380</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394931</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:B11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="460" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#173" accession="ERX1830615" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830615</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#173</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#173</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:C11, constructed from sample accession ERS1306381 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GCTCCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306381">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306381</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394932</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:C11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="442" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#174" accession="ERX1830616" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830616</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#174</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#174</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:D11, constructed from sample accession ERS1306382 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GTAAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306382">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306382</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394933</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:D11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="457" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#175" accession="ERX1830617" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830617</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#175</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#175</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:E11, constructed from sample accession ERS1306383 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GAGGATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306383">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306383</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394934</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:E11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="454" NOMINAL_SDEV="73"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#176" accession="ERX1830618" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830618</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#176</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#176</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:F11, constructed from sample accession ERS1306384 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GTTGTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306384">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306384</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394935</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:F11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="442" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#177" accession="ERX1830619" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830619</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#177</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#177</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:G11, constructed from sample accession ERS1306385 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GGATTAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306385">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306385</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394936</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:G11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="434" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#178" accession="ERX1830620" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830620</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#178</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#178</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:H11, constructed from sample accession ERS1306386 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GATAGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306386">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306386</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394937</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:H11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="421" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20957_6#180" accession="ERX1830621" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1830621</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20957_6#180</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20957_6#180</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017141">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017141</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN462207L:B12, constructed from sample accession ERS1306388 for study accession ERP017141.  This is part of an Illumina multiplexed sequencing run (20957_6).  This submission includes reads tagged with the sequence GCAATCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1306388">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1306388</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4394939</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN462207L:B12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="446" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
