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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_19536_5#69</SUBMITTER_ID>
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    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
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        <PRIMARY_ID>ERP013538</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 16220079, constructed from sample accession ERS1078793 for study accession ERP013538.  This is part of an Illumina multiplexed sequencing run (19536_5).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>ERS1078793</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3891659</EXTERNAL_ID>
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          <PAIRED NOMINAL_LENGTH="459" NOMINAL_SDEV="85"/>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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      <PRIMARY_ID>ERX1587084</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_19536_5#70</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_19536_5#70</SUBMITTER_ID>
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    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013538">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013538</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 16220091, constructed from sample accession ERS1078794 for study accession ERP013538.  This is part of an Illumina multiplexed sequencing run (19536_5).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>ERS1078794</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3891660</EXTERNAL_ID>
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        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="456" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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      <PRIMARY_ID>ERX1587085</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_19536_5#71</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_19536_5#71</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013538">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013538</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 16220103, constructed from sample accession ERS1078795 for study accession ERP013538.  This is part of an Illumina multiplexed sequencing run (19536_5).  This submission includes reads tagged with the sequence GTGTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1078795">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1078795</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3891661</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>16220103</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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  <EXPERIMENT alias="SC_EXP_19536_5#72" accession="ERX1587086" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1587086</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_19536_5#72</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_19536_5#72</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013538">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013538</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 16220115, constructed from sample accession ERS1078796 for study accession ERP013538.  This is part of an Illumina multiplexed sequencing run (19536_5).  This submission includes reads tagged with the sequence GACGGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1078796">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1078796</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3891662</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>16220115</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="457" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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  <EXPERIMENT alias="SC_EXP_19536_5#73" accession="ERX1587087" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1587087</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_19536_5#73</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_19536_5#73</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013538">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013538</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 16220032, constructed from sample accession ERS1078798 for study accession ERP013538.  This is part of an Illumina multiplexed sequencing run (19536_5).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1078798">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1078798</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3891664</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>16220032</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="434" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_19536_5#74" accession="ERX1587088" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1587088</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_19536_5#74</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_19536_5#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013538">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013538</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 16220044, constructed from sample accession ERS1078799 for study accession ERP013538.  This is part of an Illumina multiplexed sequencing run (19536_5).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1078799">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1078799</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3891665</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>16220044</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="471" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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    <IDENTIFIERS>
      <PRIMARY_ID>ERX1587089</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_19536_5#75</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_19536_5#75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013538">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013538</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 16220056, constructed from sample accession ERS1078800 for study accession ERP013538.  This is part of an Illumina multiplexed sequencing run (19536_5).  This submission includes reads tagged with the sequence GAATCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1078800">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1078800</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3891666</EXTERNAL_ID>
        </IDENTIFIERS>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>16220056</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="464" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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  <EXPERIMENT alias="SC_EXP_19536_5#76" accession="ERX1587090" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1587090</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_19536_5#76</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_19536_5#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013538">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013538</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 16220068, constructed from sample accession ERS1078801 for study accession ERP013538.  This is part of an Illumina multiplexed sequencing run (19536_5).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1078801">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1078801</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3891667</EXTERNAL_ID>
        </IDENTIFIERS>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>16220068</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="453" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <PRIMARY_ID>ERX1587091</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_19536_5#77</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_19536_5#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013538">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013538</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 16220080, constructed from sample accession ERS1078802 for study accession ERP013538.  This is part of an Illumina multiplexed sequencing run (19536_5).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1078802">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1078802</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3891668</EXTERNAL_ID>
        </IDENTIFIERS>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>16220080</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="459" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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      <PRIMARY_ID>ERX1587092</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_19536_5#78</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_19536_5#78</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013538">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013538</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 16220092, constructed from sample accession ERS1078803 for study accession ERP013538.  This is part of an Illumina multiplexed sequencing run (19536_5).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1078803">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1078803</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3891669</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>16220092</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="459" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_19536_5#79" accession="ERX1587093" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1587093</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_19536_5#79</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_19536_5#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013538">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013538</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 16220104, constructed from sample accession ERS1078804 for study accession ERP013538.  This is part of an Illumina multiplexed sequencing run (19536_5).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1078804">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1078804</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3891670</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>16220104</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="489" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_19536_5#80" accession="ERX1587094" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1587094</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_19536_5#80</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_19536_5#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013538">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013538</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 16220116, constructed from sample accession ERS1078806 for study accession ERP013538.  This is part of an Illumina multiplexed sequencing run (19536_5).  This submission includes reads tagged with the sequence GTCGCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1078806">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1078806</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3891672</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>16220116</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_19536_5#81" accession="ERX1587095" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1587095</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_19536_5#81</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_19536_5#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013538">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013538</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 16220033, constructed from sample accession ERS1078807 for study accession ERP013538.  This is part of an Illumina multiplexed sequencing run (19536_5).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1078807">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1078807</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3891673</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>16220033</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="470" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_19536_5#82" accession="ERX1587096" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1587096</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_19536_5#82</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_19536_5#82</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013538">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013538</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 16220045, constructed from sample accession ERS1078808 for study accession ERP013538.  This is part of an Illumina multiplexed sequencing run (19536_5).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1078808">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1078808</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3891674</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>16220045</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="466" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_19536_5#83" accession="ERX1587097" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1587097</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_19536_5#83</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_19536_5#83</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013538">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013538</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 16220057, constructed from sample accession ERS1078809 for study accession ERP013538.  This is part of an Illumina multiplexed sequencing run (19536_5).  This submission includes reads tagged with the sequence GCTCCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1078809">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1078809</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3891675</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>16220057</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="451" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_19536_5#84" accession="ERX1587098" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1587098</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_19536_5#84</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_19536_5#84</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013538">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013538</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 16220069, constructed from sample accession ERS1078810 for study accession ERP013538.  This is part of an Illumina multiplexed sequencing run (19536_5).  This submission includes reads tagged with the sequence GTAAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1078810">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1078810</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3891676</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>16220069</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_19536_5#85" accession="ERX1587099" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1587099</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_19536_5#85</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_19536_5#85</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013538">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013538</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 16220081, constructed from sample accession ERS1078811 for study accession ERP013538.  This is part of an Illumina multiplexed sequencing run (19536_5).  This submission includes reads tagged with the sequence GAGGATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1078811">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1078811</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3891677</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>16220081</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="464" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_19536_5#86" accession="ERX1587100" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1587100</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_19536_5#86</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_19536_5#86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013538">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013538</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 16220093, constructed from sample accession ERS1078812 for study accession ERP013538.  This is part of an Illumina multiplexed sequencing run (19536_5).  This submission includes reads tagged with the sequence GTTGTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1078812">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1078812</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3891678</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>16220093</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_19536_5#87" accession="ERX1587101" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1587101</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_19536_5#87</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_19536_5#87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013538">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013538</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 16220105, constructed from sample accession ERS1078813 for study accession ERP013538.  This is part of an Illumina multiplexed sequencing run (19536_5).  This submission includes reads tagged with the sequence GGATTAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1078813">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1078813</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3891679</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>16220105</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_19536_5#88" accession="ERX1587102" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1587102</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_19536_5#88</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_19536_5#88</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013538">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013538</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 16220117, constructed from sample accession ERS1078814 for study accession ERP013538.  This is part of an Illumina multiplexed sequencing run (19536_5).  This submission includes reads tagged with the sequence GATAGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1078814">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1078814</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3891680</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>16220117</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="460" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_19536_5#89" accession="ERX1587103" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1587103</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_19536_5#89</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_19536_5#89</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013538">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013538</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 16220034, constructed from sample accession ERS1078815 for study accession ERP013538.  This is part of an Illumina multiplexed sequencing run (19536_5).  This submission includes reads tagged with the sequence GTGTGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1078815">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1078815</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3891681</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>16220034</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="465" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_19536_5#90" accession="ERX1587104" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1587104</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_19536_5#90</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_19536_5#90</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013538">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013538</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 16220046, constructed from sample accession ERS1078816 for study accession ERP013538.  This is part of an Illumina multiplexed sequencing run (19536_5).  This submission includes reads tagged with the sequence GCAATCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1078816">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1078816</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3891682</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>16220046</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="468" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_19536_5#91" accession="ERX1587105" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1587105</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_19536_5#91</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_19536_5#91</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013538">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013538</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 16220058, constructed from sample accession ERS1078817 for study accession ERP013538.  This is part of an Illumina multiplexed sequencing run (19536_5).  This submission includes reads tagged with the sequence GACCTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1078817">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1078817</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3891683</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>16220058</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="453" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_19536_5#92" accession="ERX1587106" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1587106</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_19536_5#92</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_19536_5#92</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013538">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013538</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 16220070, constructed from sample accession ERS1078818 for study accession ERP013538.  This is part of an Illumina multiplexed sequencing run (19536_5).  This submission includes reads tagged with the sequence GCCTGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1078818">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1078818</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3891684</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>16220070</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="455" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_19536_5#93" accession="ERX1587107" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1587107</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_19536_5#93</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_19536_5#93</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013538">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013538</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 16220082, constructed from sample accession ERS1078819 for study accession ERP013538.  This is part of an Illumina multiplexed sequencing run (19536_5).  This submission includes reads tagged with the sequence GCACTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1078819">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1078819</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3891685</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>16220082</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="474" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_19536_5#94" accession="ERX1587108" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1587108</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_19536_5#94</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_19536_5#94</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP013538">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP013538</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 16220094, constructed from sample accession ERS1078820 for study accession ERP013538.  This is part of an Illumina multiplexed sequencing run (19536_5).  This submission includes reads tagged with the sequence GCTAACTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1078820">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1078820</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3891686</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>16220094</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="462" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
