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    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
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    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
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    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
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      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026066, constructed from sample accession ERS846689 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18030_1).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18030_1#5</SUBMITTER_ID>
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    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
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      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026078, constructed from sample accession ERS846690 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18030_1).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
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      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026090, constructed from sample accession ERS846691 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18030_1).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
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      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026102, constructed from sample accession ERS846692 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18030_1).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
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      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026042, constructed from sample accession ERS846687 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18030_2).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18030_2#3</SUBMITTER_ID>
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    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
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      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026054, constructed from sample accession ERS846688 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18030_2).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18030_2#4</SUBMITTER_ID>
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    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026066, constructed from sample accession ERS846689 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18030_2).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846689" refname="3615STDY6200729-sc-2404233" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846689</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539540</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200729-sc-2404233</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026066</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="175" NOMINAL_SDEV="46"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18030_2#5" accession="ERX1276909">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276909</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18030_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18030_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026078, constructed from sample accession ERS846690 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18030_2).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846690" refname="3615STDY6200730-sc-2404234" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846690</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539541</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200730-sc-2404234</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026078</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="175" NOMINAL_SDEV="46"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18030_2#6" accession="ERX1276910">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276910</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18030_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18030_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026090, constructed from sample accession ERS846691 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18030_2).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846691" refname="3615STDY6200731-sc-2404235" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846691</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539542</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200731-sc-2404235</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026090</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="175" NOMINAL_SDEV="46"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18030_2#7" accession="ERX1276911">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276911</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18030_2#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18030_2#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026102, constructed from sample accession ERS846692 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18030_2).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846692" refname="3615STDY6200732-sc-2404236" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846692</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539543</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200732-sc-2404236</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026102</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="175" NOMINAL_SDEV="46"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18031_1#1" accession="ERX1276912">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276912</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18031_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18031_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026041, constructed from sample accession ERS846679 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18031_1).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846679" refname="3615STDY6200719-sc-2404223" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846679</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539530</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200719-sc-2404223</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026041</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="171" NOMINAL_SDEV="45"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18031_1#2" accession="ERX1276913">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276913</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18031_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18031_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026053, constructed from sample accession ERS846680 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18031_1).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846680" refname="3615STDY6200720-sc-2404224" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846680</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539531</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200720-sc-2404224</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026053</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="171" NOMINAL_SDEV="45"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18031_1#3" accession="ERX1276914">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276914</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18031_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18031_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026065, constructed from sample accession ERS846681 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18031_1).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846681" refname="3615STDY6200721-sc-2404225" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846681</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539532</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200721-sc-2404225</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026065</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="171" NOMINAL_SDEV="45"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18031_1#4" accession="ERX1276915">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276915</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18031_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18031_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026077, constructed from sample accession ERS846682 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18031_1).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846682" refname="3615STDY6200722-sc-2404226" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846682</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539533</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200722-sc-2404226</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026077</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="171" NOMINAL_SDEV="45"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18031_1#5" accession="ERX1276916">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276916</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18031_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18031_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026089, constructed from sample accession ERS846683 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18031_1).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846683" refname="3615STDY6200723-sc-2404227" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846683</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539534</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200723-sc-2404227</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026089</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="171" NOMINAL_SDEV="45"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18031_1#6" accession="ERX1276917">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276917</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18031_1#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18031_1#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026101, constructed from sample accession ERS846684 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18031_1).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846684" refname="3615STDY6200724-sc-2404228" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846684</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539535</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200724-sc-2404228</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026101</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="171" NOMINAL_SDEV="45"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18031_1#7" accession="ERX1276918">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276918</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18031_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18031_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026113, constructed from sample accession ERS846685 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18031_1).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846685" refname="3615STDY6200725-sc-2404229" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846685</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539536</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200725-sc-2404229</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026113</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="171" NOMINAL_SDEV="45"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18031_2#1" accession="ERX1276919">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276919</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18031_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18031_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026041, constructed from sample accession ERS846679 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18031_2).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846679" refname="3615STDY6200719-sc-2404223" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846679</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539530</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200719-sc-2404223</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026041</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="171" NOMINAL_SDEV="44"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18031_2#2" accession="ERX1276920">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276920</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18031_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18031_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026053, constructed from sample accession ERS846680 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18031_2).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846680" refname="3615STDY6200720-sc-2404224" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846680</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539531</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200720-sc-2404224</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026053</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="171" NOMINAL_SDEV="44"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18031_2#3" accession="ERX1276921">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276921</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18031_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18031_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026065, constructed from sample accession ERS846681 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18031_2).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846681" refname="3615STDY6200721-sc-2404225" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846681</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539532</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200721-sc-2404225</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026065</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="171" NOMINAL_SDEV="44"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18031_2#4" accession="ERX1276922">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276922</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18031_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18031_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026077, constructed from sample accession ERS846682 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18031_2).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846682" refname="3615STDY6200722-sc-2404226" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846682</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539533</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200722-sc-2404226</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026077</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="171" NOMINAL_SDEV="44"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18031_2#5" accession="ERX1276923">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276923</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18031_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18031_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026089, constructed from sample accession ERS846683 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18031_2).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846683" refname="3615STDY6200723-sc-2404227" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846683</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539534</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200723-sc-2404227</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026089</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="171" NOMINAL_SDEV="44"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18031_2#6" accession="ERX1276924">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276924</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18031_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18031_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026101, constructed from sample accession ERS846684 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18031_2).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846684" refname="3615STDY6200724-sc-2404228" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846684</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539535</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200724-sc-2404228</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026101</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="171" NOMINAL_SDEV="44"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18031_2#7" accession="ERX1276925">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276925</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18031_2#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18031_2#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026113, constructed from sample accession ERS846685 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18031_2).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846685" refname="3615STDY6200725-sc-2404229" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846685</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539536</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200725-sc-2404229</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026113</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="171" NOMINAL_SDEV="44"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18036_1#1" accession="ERX1276926">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276926</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18036_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18036_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026125, constructed from sample accession ERS846686 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18036_1).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846686" refname="3615STDY6200726-sc-2404230" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846686</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539537</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200726-sc-2404230</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026125</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="176" NOMINAL_SDEV="47"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18036_1#2" accession="ERX1276927">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276927</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18036_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18036_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026042, constructed from sample accession ERS846687 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18036_1).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846687" refname="3615STDY6200727-sc-2404231" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846687</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539538</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200727-sc-2404231</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026042</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="176" NOMINAL_SDEV="47"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18036_1#3" accession="ERX1276928">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276928</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18036_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18036_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026054, constructed from sample accession ERS846688 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18036_1).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846688" refname="3615STDY6200728-sc-2404232" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846688</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539539</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200728-sc-2404232</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026054</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="176" NOMINAL_SDEV="47"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18036_1#4" accession="ERX1276929">
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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18036_1#4</SUBMITTER_ID>
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    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026066, constructed from sample accession ERS846689 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18036_1).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18036_1#5</SUBMITTER_ID>
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    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
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    </STUDY_REF>
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      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026078, constructed from sample accession ERS846690 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18036_1).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846690" refname="3615STDY6200730-sc-2404234" refcenter="SC">
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          <PAIRED NOMINAL_LENGTH="176" NOMINAL_SDEV="47"/>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18036_1#6" accession="ERX1276931">
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      <PRIMARY_ID>ERX1276931</PRIMARY_ID>
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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18036_1#6</SUBMITTER_ID>
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    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
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      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026090, constructed from sample accession ERS846691 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18036_1).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846691" refname="3615STDY6200731-sc-2404235" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846691</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539542</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200731-sc-2404235</SUBMITTER_ID>
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      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026090</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
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          <PAIRED NOMINAL_LENGTH="176" NOMINAL_SDEV="47"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18036_1#7" accession="ERX1276932">
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      <PRIMARY_ID>ERX1276932</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18036_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18036_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026102, constructed from sample accession ERS846692 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18036_1).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846692" refname="3615STDY6200732-sc-2404236" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846692</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539543</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200732-sc-2404236</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026102</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="176" NOMINAL_SDEV="47"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18036_2#1" accession="ERX1276933">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276933</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18036_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18036_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026125, constructed from sample accession ERS846686 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18036_2).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846686" refname="3615STDY6200726-sc-2404230" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846686</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539537</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200726-sc-2404230</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026125</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="176" NOMINAL_SDEV="44"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18036_2#2" accession="ERX1276934">
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      <PRIMARY_ID>ERX1276934</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18036_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18036_2#2</SUBMITTER_ID>
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    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
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      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026042, constructed from sample accession ERS846687 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18036_2).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846687" refname="3615STDY6200727-sc-2404231" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846687</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539538</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200727-sc-2404231</SUBMITTER_ID>
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        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="176" NOMINAL_SDEV="44"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18036_2#3" accession="ERX1276935">
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      <PRIMARY_ID>ERX1276935</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18036_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18036_2#3</SUBMITTER_ID>
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    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
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    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026054, constructed from sample accession ERS846688 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18036_2).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846688" refname="3615STDY6200728-sc-2404232" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846688</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539539</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200728-sc-2404232</SUBMITTER_ID>
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        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="176" NOMINAL_SDEV="44"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
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    <PLATFORM>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18036_2#4" accession="ERX1276936">
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      <PRIMARY_ID>ERX1276936</PRIMARY_ID>
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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18036_2#4</SUBMITTER_ID>
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    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026066, constructed from sample accession ERS846689 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18036_2).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846689" refname="3615STDY6200729-sc-2404233" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846689</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539540</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200729-sc-2404233</SUBMITTER_ID>
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        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="176" NOMINAL_SDEV="44"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
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    <PLATFORM>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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      <PRIMARY_ID>ERX1276937</PRIMARY_ID>
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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18036_2#5</SUBMITTER_ID>
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    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
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    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026078, constructed from sample accession ERS846690 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18036_2).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846690" refname="3615STDY6200730-sc-2404234" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846690</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539541</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200730-sc-2404234</SUBMITTER_ID>
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        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="176" NOMINAL_SDEV="44"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18036_2#6" accession="ERX1276938">
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      <PRIMARY_ID>ERX1276938</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18036_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18036_2#6</SUBMITTER_ID>
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    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026090, constructed from sample accession ERS846691 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18036_2).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846691" refname="3615STDY6200731-sc-2404235" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846691</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539542</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200731-sc-2404235</SUBMITTER_ID>
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      <LIBRARY_DESCRIPTOR>
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        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="176" NOMINAL_SDEV="44"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</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 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18036_2#7" accession="ERX1276939">
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      <PRIMARY_ID>ERX1276939</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18036_2#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18036_2#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026102, constructed from sample accession ERS846692 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18036_2).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846692" refname="3615STDY6200732-sc-2404236" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846692</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539543</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200732-sc-2404236</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026102</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="176" NOMINAL_SDEV="44"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18037_1#1" accession="ERX1276940">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276940</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18037_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18037_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026041, constructed from sample accession ERS846679 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18037_1).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846679" refname="3615STDY6200719-sc-2404223" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846679</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539530</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200719-sc-2404223</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026041</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="173" NOMINAL_SDEV="47"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18037_1#2" accession="ERX1276941">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276941</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18037_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18037_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026053, constructed from sample accession ERS846680 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18037_1).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846680" refname="3615STDY6200720-sc-2404224" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846680</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539531</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200720-sc-2404224</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026053</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="173" NOMINAL_SDEV="47"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18037_1#3" accession="ERX1276942">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276942</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18037_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18037_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026065, constructed from sample accession ERS846681 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18037_1).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846681" refname="3615STDY6200721-sc-2404225" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846681</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539532</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200721-sc-2404225</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026065</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="173" NOMINAL_SDEV="47"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18037_1#4" center_name="The Wellcome Trust Sanger Institute" accession="ERX1276943">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276943</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18037_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18037_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026077, constructed from sample accession ERS846682 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18037_1).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846682" refname="3615STDY6200722-sc-2404226" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846682</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539533</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200722-sc-2404226</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026077</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="173" NOMINAL_SDEV="47"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18037_1#5" accession="ERX1276944">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276944</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18037_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18037_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026089, constructed from sample accession ERS846683 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18037_1).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846683" refname="3615STDY6200723-sc-2404227" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846683</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539534</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200723-sc-2404227</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026089</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="173" NOMINAL_SDEV="47"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18037_1#6" accession="ERX1276945">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276945</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18037_1#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18037_1#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026101, constructed from sample accession ERS846684 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18037_1).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846684" refname="3615STDY6200724-sc-2404228" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846684</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539535</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200724-sc-2404228</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026101</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="173" NOMINAL_SDEV="47"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18037_1#7" accession="ERX1276946">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276946</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18037_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18037_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026113, constructed from sample accession ERS846685 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18037_1).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846685" refname="3615STDY6200725-sc-2404229" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846685</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539536</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200725-sc-2404229</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026113</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="173" NOMINAL_SDEV="47"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18037_2#1" accession="ERX1276947">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276947</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18037_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18037_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026041, constructed from sample accession ERS846679 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18037_2).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846679" refname="3615STDY6200719-sc-2404223" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846679</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539530</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200719-sc-2404223</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026041</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="172" NOMINAL_SDEV="45"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18037_2#2" accession="ERX1276948">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276948</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18037_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18037_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026053, constructed from sample accession ERS846680 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18037_2).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846680" refname="3615STDY6200720-sc-2404224" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846680</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539531</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200720-sc-2404224</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026053</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="172" NOMINAL_SDEV="45"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18037_2#3" accession="ERX1276949">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276949</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18037_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18037_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026065, constructed from sample accession ERS846681 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18037_2).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846681" refname="3615STDY6200721-sc-2404225" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846681</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539532</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200721-sc-2404225</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026065</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="172" NOMINAL_SDEV="45"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18037_2#4" accession="ERX1276950">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276950</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18037_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18037_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026077, constructed from sample accession ERS846682 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18037_2).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846682" refname="3615STDY6200722-sc-2404226" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846682</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539533</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200722-sc-2404226</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026077</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="172" NOMINAL_SDEV="45"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18037_2#5" accession="ERX1276951">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276951</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18037_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18037_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026089, constructed from sample accession ERS846683 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18037_2).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846683" refname="3615STDY6200723-sc-2404227" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846683</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539534</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200723-sc-2404227</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026089</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="172" NOMINAL_SDEV="45"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18037_2#6" accession="ERX1276952">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276952</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18037_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18037_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026101, constructed from sample accession ERS846684 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18037_2).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846684" refname="3615STDY6200724-sc-2404228" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846684</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539535</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200724-sc-2404228</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026101</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="172" NOMINAL_SDEV="45"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18037_2#7" accession="ERX1276953">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1276953</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18037_2#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18037_2#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010160" refname="Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010160</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Sequencing_of_Oesophageal_Mouse_Tumours_-sc-3615</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15026113, constructed from sample accession ERS846685 for study accession ERP010160.  This is part of an Illumina multiplexed sequencing run (18037_2).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS846685" refname="3615STDY6200725-sc-2404229" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS846685</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3539536</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">3615STDY6200725-sc-2404229</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15026113</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="172" NOMINAL_SDEV="45"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
