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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18418_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN423860S:E2, constructed from sample accession ERS946146 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (18418_2).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>ERS946146</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3638997</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN423860S:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_18418_2#2" accession="ERX2242374">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242374</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18418_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18418_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN423860S:F2, constructed from sample accession ERS946147 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (18418_2).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS946147">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS946147</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3638998</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN423860S:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="241" NOMINAL_SDEV="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_18418_2#3" accession="ERX2242375">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242375</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18418_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18418_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN423860S:G2, constructed from sample accession ERS946148 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (18418_2).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS946148">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS946148</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3638999</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN423860S:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="265" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_18418_2#4" accession="ERX2242376">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242376</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18418_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18418_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN423860S:H2, constructed from sample accession ERS946149 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (18418_2).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS946149">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS946149</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3639000</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN423860S:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="208" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_18418_2#5" accession="ERX2242377">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242377</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18418_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18418_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN423860S:A3, constructed from sample accession ERS946150 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (18418_2).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS946150">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS946150</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3639001</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN423860S:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="231" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_18418_2#6" accession="ERX2242378">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242378</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18418_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18418_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN423860S:B3, constructed from sample accession ERS946151 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (18418_2).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS946151">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS946151</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3639002</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN423860S:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="227" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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  <EXPERIMENT alias="SC_EXP_20604_6#1" accession="ERX2242379">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242379</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20604_6#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20604_6#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:A1, constructed from sample accession ERS1246884 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20604_6).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246884">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246884</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075774</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="333" NOMINAL_SDEV="140"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20604_6#2" accession="ERX2242380">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242380</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20604_6#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20604_6#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:B1, constructed from sample accession ERS1246885 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20604_6).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246885">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246885</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075775</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="478" NOMINAL_SDEV="185"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20604_6#3" accession="ERX2242381">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242381</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20604_6#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20604_6#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:C1, constructed from sample accession ERS1246886 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20604_6).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246886">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246886</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075776</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="371" NOMINAL_SDEV="141"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20604_6#4" accession="ERX2242382">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242382</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20604_6#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20604_6#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:D1, constructed from sample accession ERS1246887 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20604_6).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246887">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246887</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075777</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="510" NOMINAL_SDEV="187"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20604_6#5" accession="ERX2242383">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242383</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20604_6#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20604_6#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:E1, constructed from sample accession ERS1246888 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20604_6).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246888">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246888</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075778</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="424" NOMINAL_SDEV="193"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20604_6#6" accession="ERX2242384">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242384</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20604_6#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20604_6#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:F1, constructed from sample accession ERS1246889 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20604_6).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246889">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246889</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075779</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="458" NOMINAL_SDEV="160"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20604_6#7" accession="ERX2242385">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242385</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20604_6#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20604_6#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:G1, constructed from sample accession ERS1246890 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20604_6).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246890">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246890</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075780</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="424" NOMINAL_SDEV="206"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20604_6#8" accession="ERX2242386">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242386</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20604_6#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20604_6#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:H1, constructed from sample accession ERS1246891 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20604_6).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246891">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246891</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075781</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="305" NOMINAL_SDEV="100"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20604_6#9" accession="ERX2242387">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242387</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20604_6#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20604_6#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:A2, constructed from sample accession ERS1246892 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20604_6).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246892">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246892</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075782</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="474" NOMINAL_SDEV="241"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20604_6#10" accession="ERX2242388">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242388</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20604_6#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20604_6#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:B2, constructed from sample accession ERS1246893 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20604_6).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246893">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246893</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075783</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="379" NOMINAL_SDEV="163"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20604_6#11" accession="ERX2242389">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242389</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20604_6#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20604_6#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:C2, constructed from sample accession ERS1246894 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20604_6).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246894">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246894</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075784</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="381" NOMINAL_SDEV="173"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20604_6#12" accession="ERX2242390">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242390</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20604_6#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20604_6#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:D2, constructed from sample accession ERS1246895 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20604_6).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246895">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246895</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075785</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="431" NOMINAL_SDEV="136"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20617_2#1" accession="ERX2242391">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242391</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20617_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20617_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:A1, constructed from sample accession ERS1246884 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20617_2).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246884">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246884</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075774</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="328" NOMINAL_SDEV="132"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20617_2#2" accession="ERX2242392">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242392</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20617_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20617_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:B1, constructed from sample accession ERS1246885 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20617_2).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246885">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246885</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075775</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="470" NOMINAL_SDEV="180"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20617_2#3" accession="ERX2242393">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242393</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20617_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20617_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:C1, constructed from sample accession ERS1246886 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20617_2).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246886">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246886</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075776</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="362" NOMINAL_SDEV="126"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20617_2#4" accession="ERX2242394">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242394</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20617_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20617_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:D1, constructed from sample accession ERS1246887 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20617_2).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246887">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246887</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075777</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="496" NOMINAL_SDEV="182"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20617_2#5" accession="ERX2242395">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242395</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20617_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20617_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:E1, constructed from sample accession ERS1246888 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20617_2).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246888">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246888</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075778</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="408" NOMINAL_SDEV="185"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20617_2#6" accession="ERX2242396">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242396</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20617_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20617_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:F1, constructed from sample accession ERS1246889 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20617_2).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246889">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246889</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075779</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="152"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20617_2#7" accession="ERX2242397">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242397</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20617_2#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20617_2#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:G1, constructed from sample accession ERS1246890 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20617_2).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246890">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246890</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075780</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="403" NOMINAL_SDEV="193"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20617_2#8" accession="ERX2242398">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242398</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20617_2#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20617_2#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:H1, constructed from sample accession ERS1246891 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20617_2).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246891">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246891</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075781</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="301" NOMINAL_SDEV="95"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20617_2#9" accession="ERX2242399">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242399</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20617_2#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20617_2#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:A2, constructed from sample accession ERS1246892 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20617_2).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246892">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246892</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075782</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="447" NOMINAL_SDEV="230"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20617_2#10" accession="ERX2242400">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242400</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20617_2#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20617_2#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:B2, constructed from sample accession ERS1246893 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20617_2).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246893">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246893</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075783</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="372" NOMINAL_SDEV="155"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20617_2#11" accession="ERX2242401">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242401</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20617_2#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20617_2#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:C2, constructed from sample accession ERS1246894 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20617_2).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246894">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246894</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075784</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="375" NOMINAL_SDEV="166"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20617_2#12" accession="ERX2242402">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242402</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20617_2#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20617_2#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:D2, constructed from sample accession ERS1246895 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20617_2).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246895">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246895</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075785</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="425" NOMINAL_SDEV="130"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20755_8#1" accession="ERX2242403">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242403</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20755_8#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20755_8#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:A1, constructed from sample accession ERS1246884 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20755_8).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246884">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246884</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075774</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20755_8#2" accession="ERX2242404">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242404</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20755_8#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20755_8#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:B1, constructed from sample accession ERS1246885 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20755_8).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246885">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246885</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075775</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20755_8#3" accession="ERX2242405">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242405</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20755_8#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20755_8#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:G1, constructed from sample accession ERS1246890 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20755_8).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246890">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246890</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075780</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="396" NOMINAL_SDEV="179"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20755_8#4" accession="ERX2242406">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242406</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20755_8#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20755_8#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:H1, constructed from sample accession ERS1246891 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20755_8).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246891">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246891</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075781</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="302" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20850_1#2" accession="ERX2242407">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242407</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20850_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20850_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:D1, constructed from sample accession ERS1246887 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20850_1).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246887">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246887</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075777</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="480" NOMINAL_SDEV="173"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20850_1#3" accession="ERX2242408">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242408</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20850_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20850_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:E1, constructed from sample accession ERS1246888 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20850_1).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246888">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246888</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075778</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="380" NOMINAL_SDEV="158"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20850_1#4" accession="ERX2242409">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242409</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20850_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20850_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:A2, constructed from sample accession ERS1246892 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20850_1).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246892">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246892</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075782</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="416" NOMINAL_SDEV="211"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20850_1#5" accession="ERX2242410">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242410</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20850_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20850_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:B2, constructed from sample accession ERS1246893 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20850_1).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246893">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246893</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075783</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="361" NOMINAL_SDEV="136"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20850_2#1" accession="ERX2242411">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242411</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20850_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20850_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:C1, constructed from sample accession ERS1246886 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20850_2).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246886">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246886</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075776</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="364" NOMINAL_SDEV="130"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20850_2#2" accession="ERX2242412">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242412</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20850_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20850_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:D1, constructed from sample accession ERS1246887 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20850_2).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246887">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246887</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075777</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="486" NOMINAL_SDEV="176"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20850_2#3" accession="ERX2242413">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242413</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20850_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20850_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:E1, constructed from sample accession ERS1246888 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20850_2).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246888">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246888</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075778</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="382" NOMINAL_SDEV="159"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20850_2#4" accession="ERX2242414">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242414</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20850_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20850_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:A2, constructed from sample accession ERS1246892 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20850_2).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246892">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246892</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075782</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="419" NOMINAL_SDEV="215"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_20850_2#5" accession="ERX2242415">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2242415</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_20850_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_20850_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013020">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013020</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB11623</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN457801P:B2, constructed from sample accession ERS1246893 for study accession ERP013020.  This is part of an Illumina multiplexed sequencing run (20850_2).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1246893">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1246893</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4075783</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN457801P:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="362" NOMINAL_SDEV="135"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>ChIP-Seq Auto</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
