<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="SC_EXP_5505_3#1" accession="ERX2003941">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2003941</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5505_3#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5505_3#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000149">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000149</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT220347M, constructed from sample accession ERS015785 for study accession ERP000149.  This is part of an Illumina multiplexed sequencing run (5505_3).  This submission includes reads tagged with the sequence ATCACGTTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS015785">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS015785</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA864162</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT220347M</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="283" NOMINAL_SDEV="78"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer II</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_5505_3#2" accession="ERX2003942">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2003942</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_5505_3#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_5505_3#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina Genome Analyzer II paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000149">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000149</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT220348N, constructed from sample accession ERS015786 for study accession ERP000149.  This is part of an Illumina multiplexed sequencing run (5505_3).  This submission includes reads tagged with the sequence CGATGTTTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS015786">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS015786</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA864163</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT220348N</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="285" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer II</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
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