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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="ERX1087165" alias="SC_EXP_16582_1#79">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087165</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_1#79</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_1#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13436939, constructed from sample accession ERS607929 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_1).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607929" refcenter="SC" refname="2811STDY6004086-sc-2166934">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607929</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3135985</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004086-sc-2166934</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13436939</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="416" NOMINAL_SDEV="74"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087166" alias="SC_EXP_16582_1#80">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087166</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_1#80</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_1#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13436951, constructed from sample accession ERS607931 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_1).  This submission includes reads tagged with the sequence GTCGCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607931" refcenter="SC" refname="2811STDY6004087-sc-2166936">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607931</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3135987</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004087-sc-2166936</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13436951</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="416" NOMINAL_SDEV="74"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087167" alias="SC_EXP_16582_1#81">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087167</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_1#81</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_1#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13436868, constructed from sample accession ERS607933 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_1).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607933" refcenter="SC" refname="2811STDY6004088-sc-2166938">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607933</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3135989</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004088-sc-2166938</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13436868</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="416" NOMINAL_SDEV="74"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087168" alias="SC_EXP_16582_1#82">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087168</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_1#82</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_1#82</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13436880, constructed from sample accession ERS607935 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_1).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607935" refcenter="SC" refname="2811STDY6004089-sc-2166940">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607935</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3135991</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004089-sc-2166940</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13436880</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="416" NOMINAL_SDEV="74"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087169" alias="SC_EXP_16582_1#83">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087169</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_1#83</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_1#83</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13436892, constructed from sample accession ERS607937 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_1).  This submission includes reads tagged with the sequence GCTCCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607937" refcenter="SC" refname="2811STDY6004090-sc-2166942">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607937</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3135993</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004090-sc-2166942</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13436892</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="416" NOMINAL_SDEV="74"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087170" alias="SC_EXP_16582_1#84">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087170</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_1#84</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_1#84</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13436904, constructed from sample accession ERS607939 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_1).  This submission includes reads tagged with the sequence GTAAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607939" refcenter="SC" refname="2811STDY6004091-sc-2166944">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607939</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3135995</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004091-sc-2166944</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13436904</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="416" NOMINAL_SDEV="74"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087171" alias="SC_EXP_16582_2#85">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087171</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_2#85</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_2#85</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13436916, constructed from sample accession ERS607941 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_2).  This submission includes reads tagged with the sequence GAGGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607941" refcenter="SC" refname="2811STDY6004092-sc-2166946">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607941</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3135997</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004092-sc-2166946</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13436916</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="415" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087172" alias="SC_EXP_16582_2#86">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087172</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_2#86</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_2#86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13436928, constructed from sample accession ERS607943 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_2).  This submission includes reads tagged with the sequence GTTGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607943" refcenter="SC" refname="2811STDY6004093-sc-2166948">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607943</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3135999</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004093-sc-2166948</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13436928</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="415" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087173" alias="SC_EXP_16582_2#87">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087173</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_2#87</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_2#87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13436940, constructed from sample accession ERS607945 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_2).  This submission includes reads tagged with the sequence GGATTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607945" refcenter="SC" refname="2811STDY6004094-sc-2166950">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607945</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3136001</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004094-sc-2166950</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13436940</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="415" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087174" alias="SC_EXP_16582_2#88">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087174</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_2#88</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_2#88</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13436952, constructed from sample accession ERS607947 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_2).  This submission includes reads tagged with the sequence GATAGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607947" refcenter="SC" refname="2811STDY6004095-sc-2166952">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607947</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3136003</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004095-sc-2166952</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13436952</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="415" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087175" alias="SC_EXP_16582_2#89">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087175</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_2#89</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_2#89</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13436869, constructed from sample accession ERS607949 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_2).  This submission includes reads tagged with the sequence GTGTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607949" refcenter="SC" refname="2811STDY6004096-sc-2166954">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607949</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3136005</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004096-sc-2166954</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13436869</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="415" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087176" alias="SC_EXP_16582_2#90">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087176</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_2#90</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_2#90</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13436881, constructed from sample accession ERS607951 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_2).  This submission includes reads tagged with the sequence GCAATCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607951" refcenter="SC" refname="2811STDY6004097-sc-2166956">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607951</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3136007</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004097-sc-2166956</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13436881</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="415" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087177" alias="SC_EXP_16582_2#91">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087177</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_2#91</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_2#91</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13436893, constructed from sample accession ERS607953 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_2).  This submission includes reads tagged with the sequence GACCTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607953" refcenter="SC" refname="2811STDY6004098-sc-2166958">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607953</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3136009</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004098-sc-2166958</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13436893</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="415" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087178" alias="SC_EXP_16582_3#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087178</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_3#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_3#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582744, constructed from sample accession ERS607955 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_3).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607955" refcenter="SC" refname="2811STDY6004099-sc-2166960">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607955</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3136011</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004099-sc-2166960</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582744</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="438" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087179" alias="SC_EXP_16582_3#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087179</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_3#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_3#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582756, constructed from sample accession ERS607957 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_3).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607957" refcenter="SC" refname="2811STDY6004100-sc-2166962">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607957</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3136013</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004100-sc-2166962</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582756</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="438" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087180" alias="SC_EXP_16582_3#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087180</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_3#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_3#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582768, constructed from sample accession ERS607959 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_3).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607959" refcenter="SC" refname="2811STDY6004101-sc-2166964">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607959</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3136015</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004101-sc-2166964</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582768</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="438" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087181" alias="SC_EXP_16582_3#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087181</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_3#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_3#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582780, constructed from sample accession ERS607961 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_3).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607961" refcenter="SC" refname="2811STDY6004102-sc-2166966">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607961</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3136017</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004102-sc-2166966</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582780</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="438" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087182" alias="SC_EXP_16582_3#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087182</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_3#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_3#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582792, constructed from sample accession ERS607963 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_3).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607963" refcenter="SC" refname="2811STDY6004103-sc-2166968">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607963</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3136019</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004103-sc-2166968</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582792</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="438" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087183" alias="SC_EXP_16582_3#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087183</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_3#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_3#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582804, constructed from sample accession ERS607964 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_3).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607964" refcenter="SC" refname="2811STDY6004104-sc-2166969">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607964</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3136020</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004104-sc-2166969</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582804</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="438" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087184" alias="SC_EXP_16582_3#7">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087184</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_3#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_3#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582816, constructed from sample accession ERS607966 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_3).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607966" refcenter="SC" refname="2811STDY6004105-sc-2166971">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607966</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3136022</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004105-sc-2166971</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582816</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="438" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087185" alias="SC_EXP_16582_4#8">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087185</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_4#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_4#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582828, constructed from sample accession ERS607968 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_4).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607968" refcenter="SC" refname="2811STDY6004106-sc-2166973">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607968</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3136024</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004106-sc-2166973</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582828</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087186" alias="SC_EXP_16582_4#9">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087186</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_4#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_4#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582745, constructed from sample accession ERS607970 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_4).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607970" refcenter="SC" refname="2811STDY6004107-sc-2166975">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607970</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3136026</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004107-sc-2166975</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582745</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087187" alias="SC_EXP_16582_4#10">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087187</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_4#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_4#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582757, constructed from sample accession ERS607972 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_4).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607972" refcenter="SC" refname="2811STDY6004108-sc-2166977">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607972</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3136028</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004108-sc-2166977</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582757</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087188" alias="SC_EXP_16582_4#11">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087188</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_4#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_4#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582769, constructed from sample accession ERS607974 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_4).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607974" refcenter="SC" refname="2811STDY6004109-sc-2166979">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607974</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3136030</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004109-sc-2166979</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582769</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087189" alias="SC_EXP_16582_4#12">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087189</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_4#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_4#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582781, constructed from sample accession ERS607976 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_4).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607976" refcenter="SC" refname="2811STDY6004110-sc-2166981">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607976</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3136032</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004110-sc-2166981</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582781</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087190" alias="SC_EXP_16582_4#13">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087190</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_4#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_4#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582793, constructed from sample accession ERS607978 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_4).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607978" refcenter="SC" refname="2811STDY6004111-sc-2166983">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607978</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3136034</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004111-sc-2166983</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582793</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087191" alias="SC_EXP_16582_4#14">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087191</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_4#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_4#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582805, constructed from sample accession ERS607980 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_4).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607980" refcenter="SC" refname="2811STDY6004112-sc-2166985">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607980</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3136036</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004112-sc-2166985</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582805</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087192" alias="SC_EXP_16582_5#15">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087192</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_5#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_5#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582817, constructed from sample accession ERS607982 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_5).  This submission includes reads tagged with the sequence TAAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607982" refcenter="SC" refname="2811STDY6004113-sc-2166987">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607982</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3136038</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004113-sc-2166987</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582817</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087193" alias="SC_EXP_16582_5#16">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087193</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_5#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_5#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582829, constructed from sample accession ERS607984 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_5).  This submission includes reads tagged with the sequence TCCGTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607984" refcenter="SC" refname="2811STDY6004114-sc-2166989">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607984</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3136040</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004114-sc-2166989</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582829</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087194" alias="SC_EXP_16582_5#17">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087194</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_5#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_5#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582746, constructed from sample accession ERS607986 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_5).  This submission includes reads tagged with the sequence TGTACCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607986" refcenter="SC" refname="2811STDY6004115-sc-2166991">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607986</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3136042</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004115-sc-2166991</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582746</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087195" alias="SC_EXP_16582_5#18">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087195</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_5#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_5#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582758, constructed from sample accession ERS607988 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_5).  This submission includes reads tagged with the sequence TTCTGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607988" refcenter="SC" refname="2811STDY6004116-sc-2166993">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607988</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3136044</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004116-sc-2166993</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582758</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087196" alias="SC_EXP_16582_5#19">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087196</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_5#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_5#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582770, constructed from sample accession ERS607989 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_5).  This submission includes reads tagged with the sequence TCTGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607989" refcenter="SC" refname="2811STDY6004117-sc-2166994">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607989</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3136045</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004117-sc-2166994</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582770</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087197" alias="SC_EXP_16582_5#20">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087197</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_5#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_5#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582782, constructed from sample accession ERS607991 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_5).  This submission includes reads tagged with the sequence TTGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607991" refcenter="SC" refname="2811STDY6004118-sc-2166996">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607991</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3136047</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004118-sc-2166996</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582782</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087198" alias="SC_EXP_16582_5#21">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087198</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_5#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_5#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582794, constructed from sample accession ERS607993 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_5).  This submission includes reads tagged with the sequence TCGAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607993" refcenter="SC" refname="2811STDY6004119-sc-2166998">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607993</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3136049</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004119-sc-2166998</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582794</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087199" alias="SC_EXP_16582_6#22">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087199</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_6#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_6#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582806, constructed from sample accession ERS607995 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_6).  This submission includes reads tagged with the sequence TGATACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607995" refcenter="SC" refname="2811STDY6004120-sc-2167000">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607995</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3136051</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004120-sc-2167000</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582806</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="443" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087200" alias="SC_EXP_16582_6#23">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087200</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_6#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_6#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582818, constructed from sample accession ERS607997 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_6).  This submission includes reads tagged with the sequence TGCATAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607997" refcenter="SC" refname="2811STDY6004121-sc-2167002">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607997</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3136053</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004121-sc-2167002</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582818</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="443" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087201" alias="SC_EXP_16582_6#24">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087201</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_6#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_6#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582830, constructed from sample accession ERS607999 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_6).  This submission includes reads tagged with the sequence TTGACTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607999" refcenter="SC" refname="2811STDY6004122-sc-2167004">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607999</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3136055</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004122-sc-2167004</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582830</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="443" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087202" alias="SC_EXP_16582_6#25">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087202</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_6#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_6#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582747, constructed from sample accession ERS608001 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_6).  This submission includes reads tagged with the sequence TGCGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS608001" refcenter="SC" refname="2811STDY6004123-sc-2167006">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS608001</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3136057</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004123-sc-2167006</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582747</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="443" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087203" alias="SC_EXP_16582_6#26">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087203</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_6#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_6#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582759, constructed from sample accession ERS608003 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_6).  This submission includes reads tagged with the sequence TTCCTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS608003" refcenter="SC" refname="2811STDY6004124-sc-2167008">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS608003</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3136059</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004124-sc-2167008</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582759</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="443" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087204" alias="SC_EXP_16582_6#27">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087204</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_6#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_6#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582771, constructed from sample accession ERS608005 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_6).  This submission includes reads tagged with the sequence TAGTGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS608005" refcenter="SC" refname="2811STDY6004125-sc-2167010">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS608005</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3136061</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004125-sc-2167010</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582771</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="443" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087205" alias="SC_EXP_16582_6#28">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087205</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_6#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_6#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582783, constructed from sample accession ERS607817 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_6).  This submission includes reads tagged with the sequence TACAGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607817" refcenter="SC" refname="2811STDY6004126-sc-2166822">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607817</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3135873</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004126-sc-2166822</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582783</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="443" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087206" alias="SC_EXP_16582_7#29">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087206</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_7#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_7#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582795, constructed from sample accession ERS607819 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_7).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607819" refcenter="SC" refname="2811STDY6004127-sc-2166824">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607819</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3135875</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004127-sc-2166824</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582795</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087207" alias="SC_EXP_16582_7#30">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087207</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_7#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_7#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582807, constructed from sample accession ERS607821 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_7).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607821" refcenter="SC" refname="2811STDY6004128-sc-2166826">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607821</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3135877</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004128-sc-2166826</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582807</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087208" alias="SC_EXP_16582_7#31">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087208</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_7#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_7#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582819, constructed from sample accession ERS607823 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_7).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607823" refcenter="SC" refname="2811STDY6004129-sc-2166828">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607823</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3135879</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004129-sc-2166828</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582819</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087209" alias="SC_EXP_16582_7#32">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087209</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_7#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_7#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582831, constructed from sample accession ERS607825 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_7).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607825" refcenter="SC" refname="2811STDY6004130-sc-2166830">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607825</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3135881</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004130-sc-2166830</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582831</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087210" alias="SC_EXP_16582_7#33">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087210</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_7#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_7#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582748, constructed from sample accession ERS607826 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_7).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607826" refcenter="SC" refname="2811STDY6004131-sc-2166831">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607826</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3135882</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004131-sc-2166831</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582748</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087211" alias="SC_EXP_16582_7#34">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087211</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_7#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_7#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582760, constructed from sample accession ERS607828 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_7).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607828" refcenter="SC" refname="2811STDY6004132-sc-2166833">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607828</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3135884</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004132-sc-2166833</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582760</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087212" alias="SC_EXP_16582_7#35">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087212</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_7#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_7#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582772, constructed from sample accession ERS607830 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_7).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607830" refcenter="SC" refname="2811STDY6004133-sc-2166835">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607830</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3135886</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004133-sc-2166835</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582772</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087213" alias="SC_EXP_16582_8#36">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087213</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_8#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_8#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582784, constructed from sample accession ERS607832 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_8).  This submission includes reads tagged with the sequence TGAACTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607832" refcenter="SC" refname="2811STDY6004134-sc-2166837">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607832</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3135888</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004134-sc-2166837</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582784</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="447" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087214" alias="SC_EXP_16582_8#37">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087214</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_8#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_8#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582796, constructed from sample accession ERS607834 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_8).  This submission includes reads tagged with the sequence TACTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607834" refcenter="SC" refname="2811STDY6004135-sc-2166839">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607834</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3135890</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004135-sc-2166839</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582796</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="447" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087215" alias="SC_EXP_16582_8#38">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087215</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_8#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_8#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582808, constructed from sample accession ERS607836 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_8).  This submission includes reads tagged with the sequence TCTCACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607836" refcenter="SC" refname="2811STDY6004136-sc-2166841">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607836</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3135892</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004136-sc-2166841</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582808</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="447" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087216" alias="SC_EXP_16582_8#39">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087216</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_8#39</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_8#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582820, constructed from sample accession ERS607838 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_8).  This submission includes reads tagged with the sequence TCAGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607838" refcenter="SC" refname="2811STDY6004137-sc-2166843">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607838</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3135894</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004137-sc-2166843</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582820</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="447" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087217" alias="SC_EXP_16582_8#40">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087217</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_8#40</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_8#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582832, constructed from sample accession ERS607839 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_8).  This submission includes reads tagged with the sequence TAAGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607839" refcenter="SC" refname="2811STDY6004138-sc-2166844">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607839</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3135895</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004138-sc-2166844</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582832</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="447" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087218" alias="SC_EXP_16582_8#41">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087218</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_8#41</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_8#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582749, constructed from sample accession ERS607841 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_8).  This submission includes reads tagged with the sequence TCCAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607841" refcenter="SC" refname="2811STDY6004139-sc-2166846">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607841</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3135897</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004139-sc-2166846</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582749</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="447" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX1087219" alias="SC_EXP_16582_8#42">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087219</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16582_8#42</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_16582_8#42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP004086" refcenter="SC" refname="CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP004086</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CGP_C_elegans_whole_genomes_PART2-sc-2013-10-16T11:52:24Z-2811</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13582761, constructed from sample accession ERS607843 for study accession ERP004086.  This is part of an Illumina multiplexed sequencing run (16582_8).  This submission includes reads tagged with the sequence TGTATGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS607843" refcenter="SC" refname="2811STDY6004140-sc-2166848">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS607843</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3135899</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2811STDY6004140-sc-2166848</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13582761</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="447" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
