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      <SUBMITTER_ID namespace="SC">SC_EXP_18512_8#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18512_8#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP002418">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP002418</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15377282, constructed from sample accession ERS986226 for study accession ERP002418.  This is part of an Illumina multiplexed sequencing run (18512_8).  This submission includes reads tagged with the sequence CAACGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS986226">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS986226</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3679077</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15377282</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="113"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18512_8#2" accession="ERX1414583" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1414583</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18512_8#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18512_8#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP002418">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP002418</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15377284, constructed from sample accession ERS986228 for study accession ERP002418.  This is part of an Illumina multiplexed sequencing run (18512_8).  This submission includes reads tagged with the sequence CTGAGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS986228">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS986228</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3679079</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15377284</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="113"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18512_8#3" accession="ERX1414584" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1414584</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18512_8#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18512_8#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP002418">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP002418</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15377286, constructed from sample accession ERS986230 for study accession ERP002418.  This is part of an Illumina multiplexed sequencing run (18512_8).  This submission includes reads tagged with the sequence GACGTACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS986230">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS986230</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3679081</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15377286</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="113"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
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      <PRIMARY_ID>ERX1414585</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18512_8#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18512_8#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP002418">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP002418</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15377288, constructed from sample accession ERS986232 for study accession ERP002418.  This is part of an Illumina multiplexed sequencing run (18512_8).  This submission includes reads tagged with the sequence GGTAGAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS986232">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS986232</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3679083</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15377288</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="113"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18512_8#5" accession="ERX1414586" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1414586</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18512_8#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18512_8#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP002418">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP002418</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15377289, constructed from sample accession ERS986233 for study accession ERP002418.  This is part of an Illumina multiplexed sequencing run (18512_8).  This submission includes reads tagged with the sequence TCGTTCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS986233">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS986233</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3679084</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15377289</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="113"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18512_8#6" accession="ERX1414587" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1414587</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18512_8#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18512_8#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP002418">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP002418</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15377283, constructed from sample accession ERS986227 for study accession ERP002418.  This is part of an Illumina multiplexed sequencing run (18512_8).  This submission includes reads tagged with the sequence CCGATCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS986227">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS986227</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3679078</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15377283</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="113"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18512_8#7" accession="ERX1414588" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1414588</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18512_8#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18512_8#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP002418">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP002418</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15377285, constructed from sample accession ERS986229 for study accession ERP002418.  This is part of an Illumina multiplexed sequencing run (18512_8).  This submission includes reads tagged with the sequence GAACGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS986229">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS986229</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3679080</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15377285</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="113"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18512_8#8" accession="ERX1414589" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1414589</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18512_8#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18512_8#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP002418">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP002418</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15377287, constructed from sample accession ERS986231 for study accession ERP002418.  This is part of an Illumina multiplexed sequencing run (18512_8).  This submission includes reads tagged with the sequence GCTGGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS986231">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS986231</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3679082</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15377287</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="113"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18512_8#9" accession="ERX1414590" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1414590</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18512_8#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18512_8#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP002418">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP002418</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15377290, constructed from sample accession ERS986234 for study accession ERP002418.  This is part of an Illumina multiplexed sequencing run (18512_8).  This submission includes reads tagged with the sequence TTAGGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS986234">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS986234</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3679085</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15377290</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="113"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18512_8#10" accession="ERX1414591" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1414591</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18512_8#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18512_8#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP002418">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP002418</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15377291, constructed from sample accession ERS986235 for study accession ERP002418.  This is part of an Illumina multiplexed sequencing run (18512_8).  This submission includes reads tagged with the sequence AACCTGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS986235">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS986235</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3679086</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15377291</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="113"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18512_8#11" accession="ERX1414592" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1414592</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18512_8#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18512_8#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP002418">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP002418</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15377292, constructed from sample accession ERS986236 for study accession ERP002418.  This is part of an Illumina multiplexed sequencing run (18512_8).  This submission includes reads tagged with the sequence AGAACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS986236">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS986236</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3679087</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15377292</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="113"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_18512_8#12" accession="ERX1414593" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1414593</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_18512_8#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_18512_8#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP002418">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP002418</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 15377293, constructed from sample accession ERS986237 for study accession ERP002418.  This is part of an Illumina multiplexed sequencing run (18512_8).  This submission includes reads tagged with the sequence GTTGCAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS986237">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS986237</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3679088</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15377293</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="113"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
