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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="SC_EXP_21479_1#1" accession="ERX1943055" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943055</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868923S, constructed from sample accession ERS1454954 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence CGAGAGTTATCGTACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454954">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454954</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555775</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868923S</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#2" accession="ERX1943056" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943056</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868931S, constructed from sample accession ERS1454962 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence GACATAGTATCGTACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454962">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454962</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555783</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868931S</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#3" accession="ERX1943057" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943057</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868924T, constructed from sample accession ERS1454955 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence CGAGAGTTACTATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454955">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454955</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555776</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868924T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#4" accession="ERX1943058" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943058</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868932T, constructed from sample accession ERS1454963 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence GACATAGTACTATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454963">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454963</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555784</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868932T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#5" accession="ERX1943059" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943059</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868925U, constructed from sample accession ERS1454956 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence CGAGAGTTTAGCGAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454956">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454956</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555777</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868925U</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#6" accession="ERX1943060" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943060</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868933U, constructed from sample accession ERS1454964 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence GACATAGTTAGCGAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454964">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454964</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555785</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868933U</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#7" accession="ERX1943061" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943061</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868926V, constructed from sample accession ERS1454957 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence CGAGAGTTCTGCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454957">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454957</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555778</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868926V</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#8" accession="ERX1943062" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943062</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868934V, constructed from sample accession ERS1454965 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence GACATAGTCTGCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454965">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454965</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555786</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868934V</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#9" accession="ERX1943063" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943063</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868927W, constructed from sample accession ERS1454958 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence CGAGAGTTTCATCGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454958">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454958</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555779</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868927W</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#10" accession="ERX1943064" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943064</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868935W, constructed from sample accession ERS1454966 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence GACATAGTTCATCGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454966">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454966</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555787</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868935W</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#11" accession="ERX1943065" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943065</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868928A, constructed from sample accession ERS1454959 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence CGAGAGTTCGTGAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454959">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454959</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555780</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868928A</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#12" accession="ERX1943066" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943066</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868936A, constructed from sample accession ERS1454967 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence GACATAGTCGTGAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454967">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454967</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555788</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868936A</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#13" accession="ERX1943067" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943067</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868929B, constructed from sample accession ERS1454960 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence CGAGAGTTGGATATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454960">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454960</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555781</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868929B</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#14" accession="ERX1943068" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943068</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868937B, constructed from sample accession ERS1454968 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence GACATAGTGGATATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454968">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454968</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555789</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868937B</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#15" accession="ERX1943069" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943069</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868930R, constructed from sample accession ERS1454961 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence CGAGAGTTGACACCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454961">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454961</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555782</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868930R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#16" accession="ERX1943070" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943070</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868938C, constructed from sample accession ERS1454969 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence GACATAGTGACACCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454969">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454969</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555790</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868938C</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#17" accession="ERX1943071" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943071</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868827T, constructed from sample accession ERS1454858 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence TACTAGGTAAGCAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454858">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454858</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555679</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868827T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#18" accession="ERX1943072" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943072</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868828U, constructed from sample accession ERS1454859 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence TACTAGGTACGCGTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454859">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454859</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555680</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868828U</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#19" accession="ERX1943073" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943073</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868829V, constructed from sample accession ERS1454860 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence TACTAGGTCGATCTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454860">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454860</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555681</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868829V</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#20" accession="ERX1943074" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943074</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868830O, constructed from sample accession ERS1454861 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence TACTAGGTTGCGTCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454861">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454861</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555682</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868830O</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#21" accession="ERX1943075" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943075</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868831P, constructed from sample accession ERS1454862 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence TACTAGGTGTCTAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454862">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454862</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555683</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868831P</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#22" accession="ERX1943076" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943076</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868832Q, constructed from sample accession ERS1454863 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence TACTAGGTCTAGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454863">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454863</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555684</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868832Q</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#23" accession="ERX1943077" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943077</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868833R, constructed from sample accession ERS1454864 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence TACTAGGTGATAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454864">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454864</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555685</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868833R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#24" accession="ERX1943078" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943078</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868834S, constructed from sample accession ERS1454865 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence TACTAGGTTCTACACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454865">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454865</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555686</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868834S</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#25" accession="ERX1943079" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943079</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868835T, constructed from sample accession ERS1454866 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence ACGTACGTAAGCAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454866">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454866</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555687</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868835T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#26" accession="ERX1943080" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943080</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868836U, constructed from sample accession ERS1454867 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence ACGTACGTACGCGTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454867">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454867</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555688</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868836U</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#27" accession="ERX1943081" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943081</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868837V, constructed from sample accession ERS1454868 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence ACGTACGTCGATCTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454868">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454868</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555689</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868837V</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#28" accession="ERX1943082" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943082</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868838W, constructed from sample accession ERS1454869 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence ACGTACGTTGCGTCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454869">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454869</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555690</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868838W</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#29" accession="ERX1943083" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943083</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868839A, constructed from sample accession ERS1454870 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence ACGTACGTGTCTAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454870">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454870</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555691</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868839A</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#30" accession="ERX1943084" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943084</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868840Q, constructed from sample accession ERS1454871 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence ACGTACGTCTAGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454871">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454871</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555692</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868840Q</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#31" accession="ERX1943085" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943085</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868841R, constructed from sample accession ERS1454872 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence ACGTACGTGATAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454872">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454872</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555693</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868841R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#32" accession="ERX1943086" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943086</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868842S, constructed from sample accession ERS1454873 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence ACGTACGTTCTACACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454873">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454873</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555694</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868842S</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#33" accession="ERX1943087" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943087</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868843T, constructed from sample accession ERS1454874 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence CGCGATATAAGCAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454874">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454874</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555695</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868843T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#34" accession="ERX1943088" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943088</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868844U, constructed from sample accession ERS1454875 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence CGCGATATACGCGTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454875">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454875</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555696</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868844U</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#35" accession="ERX1943089" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943089</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868845V, constructed from sample accession ERS1454876 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence CGCGATATCGATCTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454876">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454876</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555697</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868845V</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#36" accession="ERX1943090" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943090</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868846W, constructed from sample accession ERS1454877 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence CGCGATATTGCGTCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454877">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454877</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555698</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868846W</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#37" accession="ERX1943091" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943091</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868847A, constructed from sample accession ERS1454878 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence CGCGATATGTCTAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454878">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454878</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555699</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868847A</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#38" accession="ERX1943092" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943092</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868848B, constructed from sample accession ERS1454879 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence CGCGATATCTAGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454879">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454879</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555700</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868848B</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#39" accession="ERX1943093" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943093</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#39</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868849C, constructed from sample accession ERS1454880 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence CGCGATATGATAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454880">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454880</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555701</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868849C</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#40" accession="ERX1943094" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943094</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#40</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868850S, constructed from sample accession ERS1454881 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence CGCGATATTCTACACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454881">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454881</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555702</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868850S</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#41" accession="ERX1943095" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943095</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#41</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868851T, constructed from sample accession ERS1454882 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence CTATCGTGAAGCAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454882">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454882</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555703</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868851T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#42" accession="ERX1943096" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943096</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#42</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868852U, constructed from sample accession ERS1454883 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence CTATCGTGACGCGTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454883">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454883</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555704</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868852U</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#43" accession="ERX1943097" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943097</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#43</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868853V, constructed from sample accession ERS1454884 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence CTATCGTGCGATCTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454884">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454884</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555705</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868853V</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#44" accession="ERX1943098" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943098</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#44</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868854W, constructed from sample accession ERS1454885 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence CTATCGTGTGCGTCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454885">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454885</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555706</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868854W</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#45" accession="ERX1943099" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943099</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#45</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868855A, constructed from sample accession ERS1454886 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence CTATCGTGGTCTAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454886">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454886</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555707</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868855A</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#46" accession="ERX1943100" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943100</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#46</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868856B, constructed from sample accession ERS1454887 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence CTATCGTGCTAGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454887">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454887</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555708</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868856B</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#47" accession="ERX1943101" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943101</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#47</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868857C, constructed from sample accession ERS1454888 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence CTATCGTGGATAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454888">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454888</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555709</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868857C</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#48" accession="ERX1943102" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943102</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#48</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868858D, constructed from sample accession ERS1454889 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence CTATCGTGTCTACACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454889">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454889</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555710</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868858D</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#49" accession="ERX1943103" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943103</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#49</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868859E, constructed from sample accession ERS1454890 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence GCGATACGAAGCAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454890">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454890</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555711</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868859E</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#50" accession="ERX1943104" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943104</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#50</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868860U, constructed from sample accession ERS1454891 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence GCGATACGACGCGTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454891">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454891</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555712</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868860U</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#51" accession="ERX1943105" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943105</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#51</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868861V, constructed from sample accession ERS1454892 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence GCGATACGCGATCTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454892">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454892</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555713</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868861V</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#52" accession="ERX1943106" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943106</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#52</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868862W, constructed from sample accession ERS1454893 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence GCGATACGTGCGTCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454893">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454893</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555714</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868862W</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#53" accession="ERX1943107" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943107</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#53</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868863A, constructed from sample accession ERS1454894 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence GCGATACGGTCTAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454894">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454894</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555715</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868863A</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#54" accession="ERX1943108" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943108</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#54</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868864B, constructed from sample accession ERS1454895 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence GCGATACGCTAGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454895">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454895</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555716</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868864B</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#55" accession="ERX1943109" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943109</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#55</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868865C, constructed from sample accession ERS1454896 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence GCGATACGGATAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454896">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454896</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555717</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868865C</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#56" accession="ERX1943110" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943110</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#56</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868866D, constructed from sample accession ERS1454897 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence GCGATACGTCTACACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454897">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454897</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555718</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868866D</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#57" accession="ERX1943111" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943111</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#57</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868867E, constructed from sample accession ERS1454898 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence AGTCGCAGAAGCAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454898">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454898</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555719</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868867E</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#58" accession="ERX1943112" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943112</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#58</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868868F, constructed from sample accession ERS1454899 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence AGTCGCAGACGCGTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454899">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454899</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555720</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868868F</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#59" accession="ERX1943113" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943113</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#59</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868869G, constructed from sample accession ERS1454900 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence AGTCGCAGCGATCTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454900">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454900</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555721</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868869G</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#60" accession="ERX1943114" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943114</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#60</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#60</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868870W, constructed from sample accession ERS1454901 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence AGTCGCAGTGCGTCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454901">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454901</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555722</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868870W</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#61" accession="ERX1943115" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943115</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#61</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868871A, constructed from sample accession ERS1454902 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence AGTCGCAGGTCTAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454902">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454902</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555723</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868871A</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#62" accession="ERX1943116" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943116</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#62</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868872B, constructed from sample accession ERS1454903 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence AGTCGCAGCTAGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454903">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454903</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555724</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868872B</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#63" accession="ERX1943117" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943117</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#63</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#63</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868873C, constructed from sample accession ERS1454904 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence AGTCGCAGGATAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454904">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454904</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555725</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868873C</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#64" accession="ERX1943118" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943118</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#64</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#64</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868874D, constructed from sample accession ERS1454905 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence AGTCGCAGTCTACACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454905">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454905</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555726</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868874D</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#65" accession="ERX1943119" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943119</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#65</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#65</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868875E, constructed from sample accession ERS1454906 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence GTTACAGCAAGCAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454906">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454906</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555727</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868875E</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#66" accession="ERX1943120" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943120</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#66</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#66</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868876F, constructed from sample accession ERS1454907 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence GTTACAGCACGCGTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454907">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454907</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555728</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868876F</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#67" accession="ERX1943121" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943121</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#67</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868877G, constructed from sample accession ERS1454908 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence GTTACAGCCGATCTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454908">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454908</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555729</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868877G</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#68" accession="ERX1943122" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943122</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#68</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868878H, constructed from sample accession ERS1454909 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence GTTACAGCTGCGTCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454909">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454909</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555730</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868878H</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#69" accession="ERX1943123" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943123</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#69</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#69</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868879I, constructed from sample accession ERS1454910 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence GTTACAGCGTCTAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454910">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454910</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555731</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868879I</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#70" accession="ERX1943124" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943124</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#70</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#70</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868880B, constructed from sample accession ERS1454911 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence GTTACAGCCTAGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454911">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454911</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555732</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868880B</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#71" accession="ERX1943125" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943125</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#71</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#71</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868881C, constructed from sample accession ERS1454912 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence GTTACAGCGATAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454912">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454912</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555733</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868881C</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#72" accession="ERX1943126" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943126</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#72</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#72</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868882D, constructed from sample accession ERS1454913 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence GTTACAGCTCTACACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454913">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454913</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555734</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868882D</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#73" accession="ERX1943127" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943127</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#73</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#73</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868883E, constructed from sample accession ERS1454914 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence TAACGTCCAAGCAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454914">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454914</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555735</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868883E</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#74" accession="ERX1943128" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943128</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#74</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868884F, constructed from sample accession ERS1454915 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence TAACGTCCACGCGTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454915">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454915</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555736</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868884F</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#75" accession="ERX1943129" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943129</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#75</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868885G, constructed from sample accession ERS1454916 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence TAACGTCCCGATCTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454916">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454916</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555737</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868885G</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#76" accession="ERX1943130" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943130</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#76</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868886H, constructed from sample accession ERS1454917 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence TAACGTCCTGCGTCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454917">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454917</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555738</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868886H</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#77" accession="ERX1943131" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943131</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#77</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868887I, constructed from sample accession ERS1454918 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence TAACGTCCGTCTAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454918">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454918</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555739</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868887I</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#78" accession="ERX1943132" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943132</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#78</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#78</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868888J, constructed from sample accession ERS1454919 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence TAACGTCCCTAGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454919">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454919</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555740</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868888J</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#79" accession="ERX1943133" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943133</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#79</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868889K, constructed from sample accession ERS1454920 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence TAACGTCCGATAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454920">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454920</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555741</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868889K</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#80" accession="ERX1943134" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943134</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#80</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868890D, constructed from sample accession ERS1454921 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence TAACGTCCTCTACACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454921">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454921</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555742</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868890D</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#81" accession="ERX1943135" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943135</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#81</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868891E, constructed from sample accession ERS1454922 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence CTACGACCAAGCAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454922">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454922</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555743</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868891E</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#82" accession="ERX1943136" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943136</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#82</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#82</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868892F, constructed from sample accession ERS1454923 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence CTACGACCACGCGTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454923">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454923</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555744</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868892F</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#83" accession="ERX1943137" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943137</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#83</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#83</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868893G, constructed from sample accession ERS1454924 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence CTACGACCCGATCTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454924">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454924</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555745</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868893G</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#84" accession="ERX1943138" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943138</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#84</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#84</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868894H, constructed from sample accession ERS1454925 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence CTACGACCTGCGTCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454925">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454925</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555746</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868894H</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#85" accession="ERX1943139" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943139</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#85</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#85</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868895I, constructed from sample accession ERS1454926 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence CTACGACCGTCTAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454926">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454926</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555747</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868895I</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#86" accession="ERX1943140" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943140</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#86</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868896J, constructed from sample accession ERS1454927 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence CTACGACCCTAGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454927">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454927</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555748</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868896J</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#87" accession="ERX1943141" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943141</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#87</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868897K, constructed from sample accession ERS1454928 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence CTACGACCGATAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454928">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454928</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555749</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868897K</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#88" accession="ERX1943142" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943142</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#88</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#88</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868898L, constructed from sample accession ERS1454929 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence CTACGACCTCTACACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454929">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454929</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555750</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868898L</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#89" accession="ERX1943143" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943143</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#89</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#89</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868899M, constructed from sample accession ERS1454930 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence GAGACTTAAAGCAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454930">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454930</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555751</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868899M</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#90" accession="ERX1943144" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943144</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#90</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#90</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868900L, constructed from sample accession ERS1454931 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence GAGACTTAACGCGTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454931">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454931</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555752</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868900L</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#91" accession="ERX1943145" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943145</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#91</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#91</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868901M, constructed from sample accession ERS1454932 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence GAGACTTACGATCTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454932">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454932</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555753</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868901M</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#92" accession="ERX1943146" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943146</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#92</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#92</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868902N, constructed from sample accession ERS1454933 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence GAGACTTATGCGTCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454933">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454933</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555754</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868902N</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#93" accession="ERX1943147" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943147</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#93</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#93</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868903O, constructed from sample accession ERS1454934 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence GAGACTTAGTCTAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454934">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454934</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555755</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868903O</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#94" accession="ERX1943148" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943148</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#94</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#94</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868904P, constructed from sample accession ERS1454935 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence GAGACTTACTAGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454935">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454935</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555756</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868904P</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#95" accession="ERX1943149" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943149</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#95</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#95</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868905Q, constructed from sample accession ERS1454936 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence GAGACTTAGATAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454936">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454936</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555757</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868905Q</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#96" accession="ERX1943150" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943150</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#96</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#96</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868906R, constructed from sample accession ERS1454937 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence GAGACTTATCTACACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454937">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454937</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555758</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868906R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#97" accession="ERX1943151" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943151</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#97</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#97</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868907S, constructed from sample accession ERS1454938 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence ACTGTGTAAAGCAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454938">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454938</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555759</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868907S</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#98" accession="ERX1943152" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943152</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#98</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#98</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868908T, constructed from sample accession ERS1454939 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence ACTGTGTAACGCGTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454939">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454939</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555760</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868908T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#99" accession="ERX1943153" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943153</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#99</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#99</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868909U, constructed from sample accession ERS1454940 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence ACTGTGTACGATCTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454940">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454940</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555761</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868909U</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#100" accession="ERX1943154" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943154</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#100</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868910N, constructed from sample accession ERS1454941 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence ACTGTGTATGCGTCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454941">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454941</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555762</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868910N</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#101" accession="ERX1943155" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943155</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#101</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#101</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868911O, constructed from sample accession ERS1454942 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence ACTGTGTAGTCTAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454942">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454942</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555763</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868911O</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#102" accession="ERX1943156" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943156</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#102</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#102</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868912P, constructed from sample accession ERS1454943 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence ACTGTGTACTAGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454943">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454943</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555764</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868912P</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#103" accession="ERX1943157" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943157</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#103</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#103</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868913Q, constructed from sample accession ERS1454944 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence ACTGTGTAGATAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454944">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454944</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555765</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868913Q</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#104" accession="ERX1943158" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943158</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#104</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#104</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868914R, constructed from sample accession ERS1454945 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence ACTGTGTATCTACACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454945">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454945</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555766</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868914R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#105" accession="ERX1943159" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943159</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#105</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#105</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868915S, constructed from sample accession ERS1454946 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence TGCGTCAAAAGCAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454946">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454946</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555767</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868915S</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#106" accession="ERX1943160" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943160</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#106</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#106</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868916T, constructed from sample accession ERS1454947 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence TGCGTCAAACGCGTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454947">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454947</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555768</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868916T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#107" accession="ERX1943161" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943161</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#107</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#107</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868917U, constructed from sample accession ERS1454948 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence TGCGTCAACGATCTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454948">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454948</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555769</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868917U</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#108" accession="ERX1943162" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943162</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#108</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#108</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868918V, constructed from sample accession ERS1454949 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence TGCGTCAATGCGTCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454949">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454949</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555770</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868918V</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#109" accession="ERX1943163" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943163</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#109</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#109</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868919W, constructed from sample accession ERS1454950 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence TGCGTCAAGTCTAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454950">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454950</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555771</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868919W</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#110" accession="ERX1943164" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943164</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#110</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#110</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868920P, constructed from sample accession ERS1454951 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence TGCGTCAACTAGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454951">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454951</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555772</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868920P</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#111" accession="ERX1943165" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943165</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#111</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#111</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868921Q, constructed from sample accession ERS1454952 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence TGCGTCAAGATAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454952">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454952</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555773</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868921Q</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21479_1#112" accession="ERX1943166" broker_name="">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1943166</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21479_1#112</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_21479_1#112</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016546">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016546</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT868922R, constructed from sample accession ERS1454953 for study accession ERP016546.  This is part of an Illumina multiplexed sequencing run (21479_1).  This submission includes reads tagged with the sequence TGCGTCAATCTACACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1454953">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1454953</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4555774</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT868922R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
