<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="SC_EXP_14847_6#47" center_name="The Wellcome Trust Sanger Institute" accession="ERX698675">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698675</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#47</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056794, constructed from sample accession ERS540761 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540761" refname="SC_MFY5867787-sc-2002493" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540761</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752164</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867787-sc-2002493</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056794</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#48" center_name="The Wellcome Trust Sanger Institute" accession="ERX698676">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698676</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#48</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056806, constructed from sample accession ERS540762 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540762" refname="SC_MFY5867876-sc-2002494" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540762</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752165</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867876-sc-2002494</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056806</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#49" center_name="The Wellcome Trust Sanger Institute" accession="ERX698677">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698677</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#49</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056723, constructed from sample accession ERS540764 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540764" refname="SC_MFY5867877-sc-2002498" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540764</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752167</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867877-sc-2002498</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056723</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#50" center_name="The Wellcome Trust Sanger Institute" accession="ERX698678">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698678</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#50</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056735, constructed from sample accession ERS540763 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540763" refname="SC_MFY5867788-sc-2002497" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540763</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752166</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867788-sc-2002497</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056735</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#51" center_name="The Wellcome Trust Sanger Institute" accession="ERX698679">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698679</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#51</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056747, constructed from sample accession ERS540765 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540765" refname="SC_MFY5867789-sc-2002501" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540765</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752168</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867789-sc-2002501</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056747</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#52" center_name="The Wellcome Trust Sanger Institute" accession="ERX698680">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698680</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#52</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056759, constructed from sample accession ERS540766 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540766" refname="SC_MFY5867878-sc-2002502" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540766</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752169</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867878-sc-2002502</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056759</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#53" center_name="The Wellcome Trust Sanger Institute" accession="ERX698681">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698681</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#53</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056771, constructed from sample accession ERS540767 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540767" refname="SC_MFY5867879-sc-2002504" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540767</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752170</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867879-sc-2002504</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056771</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#54" center_name="The Wellcome Trust Sanger Institute" accession="ERX698682">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698682</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#54</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056783, constructed from sample accession ERS540768 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540768" refname="SC_MFY5867790-sc-2002507" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540768</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752171</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867790-sc-2002507</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056783</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#55" center_name="The Wellcome Trust Sanger Institute" accession="ERX698683">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698683</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#55</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056795, constructed from sample accession ERS540769 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540769" refname="SC_MFY5867880-sc-2002508" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540769</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752172</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867880-sc-2002508</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056795</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#56" center_name="The Wellcome Trust Sanger Institute" accession="ERX698684">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698684</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#56</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056807, constructed from sample accession ERS540770 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540770" refname="SC_MFY5867791-sc-2002509" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540770</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752173</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867791-sc-2002509</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056807</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#57" center_name="The Wellcome Trust Sanger Institute" accession="ERX698685">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698685</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#57</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056724, constructed from sample accession ERS540771 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540771" refname="SC_MFY5867881-sc-2002513" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540771</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752174</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867881-sc-2002513</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056724</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#58" center_name="The Wellcome Trust Sanger Institute" accession="ERX698686">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698686</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#58</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056736, constructed from sample accession ERS540772 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540772" refname="SC_MFY5867792-sc-2002514" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540772</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752175</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867792-sc-2002514</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056736</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </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="ERX698867" alias="SC_EXP_14847_8#49" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698867</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039705, constructed from sample accession ERS510115 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510115">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510115</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660913</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039705</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698868" alias="SC_EXP_14847_8#50" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698868</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039717, constructed from sample accession ERS510116 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510116">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510116</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660914</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039717</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698869" alias="SC_EXP_14847_8#51" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698869</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039729, constructed from sample accession ERS510117 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510117">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510117</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660915</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039729</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698870" alias="SC_EXP_14847_8#52" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698870</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039741, constructed from sample accession ERS510118 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510118">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510118</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660916</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039741</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698871" alias="SC_EXP_14847_8#53" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698871</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039753, constructed from sample accession ERS510119 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510119">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510119</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660917</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039753</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698872" alias="SC_EXP_14847_8#54" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698872</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039765, constructed from sample accession ERS510120 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510120">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510120</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660918</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039765</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698873" alias="SC_EXP_14847_8#55" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698873</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039777, constructed from sample accession ERS510121 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510121">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510121</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660919</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039777</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698874" alias="SC_EXP_14847_8#56" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698874</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039789, constructed from sample accession ERS510122 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510122">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510122</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660920</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039789</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698875" alias="SC_EXP_14847_8#57" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698875</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039706, constructed from sample accession ERS510123 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510123">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510123</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660921</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039706</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698876" alias="SC_EXP_14847_8#58" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698876</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039718, constructed from sample accession ERS510124 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510124">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510124</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660922</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039718</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698877" alias="SC_EXP_14847_8#59" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698877</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039730, constructed from sample accession ERS510125 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510125">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510125</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660923</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039730</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698878" alias="SC_EXP_14847_8#60" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698878</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#60</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039742, constructed from sample accession ERS510126 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510126">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510126</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660924</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039742</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#59" center_name="The Wellcome Trust Sanger Institute" accession="ERX698687">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698687</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#59</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056748, constructed from sample accession ERS540774 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540774" refname="SC_MFY5867882-sc-2002518" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540774</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752177</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867882-sc-2002518</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056748</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#60" center_name="The Wellcome Trust Sanger Institute" accession="ERX698688">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698688</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#60</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#60</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056760, constructed from sample accession ERS540773 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540773" refname="SC_MFY5867793-sc-2002517" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540773</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752176</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867793-sc-2002517</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056760</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#61" center_name="The Wellcome Trust Sanger Institute" accession="ERX698689">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698689</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#61</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056772, constructed from sample accession ERS540775 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540775" refname="SC_MFY5867794-sc-2002520" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540775</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752178</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867794-sc-2002520</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056772</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#62" center_name="The Wellcome Trust Sanger Institute" accession="ERX698690">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698690</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#62</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056784, constructed from sample accession ERS540776 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540776" refname="SC_MFY5867883-sc-2002521" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540776</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752179</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867883-sc-2002521</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056784</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#63" center_name="The Wellcome Trust Sanger Institute" accession="ERX698691">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698691</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#63</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#63</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056796, constructed from sample accession ERS540777 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540777" refname="SC_MFY5867795-sc-2002523" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540777</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752180</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867795-sc-2002523</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056796</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#64" center_name="The Wellcome Trust Sanger Institute" accession="ERX698692">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698692</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#64</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#64</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056808, constructed from sample accession ERS540778 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540778" refname="SC_MFY5867884-sc-2002524" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540778</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752181</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867884-sc-2002524</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056808</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#65" center_name="The Wellcome Trust Sanger Institute" accession="ERX698693">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698693</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#65</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#65</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056725, constructed from sample accession ERS540780 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540780" refname="SC_MFY5867885-sc-2002527" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540780</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752183</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867885-sc-2002527</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056725</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#66" center_name="The Wellcome Trust Sanger Institute" accession="ERX698694">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698694</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#66</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#66</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056737, constructed from sample accession ERS540779 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540779" refname="SC_MFY5867796-sc-2002526" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540779</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752182</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867796-sc-2002526</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056737</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#67" center_name="The Wellcome Trust Sanger Institute" accession="ERX698695">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698695</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#67</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056749, constructed from sample accession ERS540781 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540781" refname="SC_MFY5867797-sc-2002529" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540781</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752184</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867797-sc-2002529</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056749</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#68" center_name="The Wellcome Trust Sanger Institute" accession="ERX698696">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698696</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#68</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056761, constructed from sample accession ERS540782 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540782" refname="SC_MFY5867886-sc-2002530" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540782</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752185</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867886-sc-2002530</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056761</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#69" center_name="The Wellcome Trust Sanger Institute" accession="ERX698697">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698697</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#69</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#69</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056773, constructed from sample accession ERS540783 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540783" refname="SC_MFY5867887-sc-2002532" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540783</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752186</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867887-sc-2002532</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056773</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#70" center_name="The Wellcome Trust Sanger Institute" accession="ERX698698">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698698</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#70</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#70</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056785, constructed from sample accession ERS540784 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540784" refname="SC_MFY5867798-sc-2002533" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540784</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752187</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867798-sc-2002533</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056785</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </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="ERX698879" alias="SC_EXP_14847_8#61" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698879</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039754, constructed from sample accession ERS510127 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510127">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510127</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660925</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039754</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698880" alias="SC_EXP_14847_8#62" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698880</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039766, constructed from sample accession ERS510128 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510128">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510128</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660926</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039766</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698881" alias="SC_EXP_14847_8#63" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698881</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#63</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039778, constructed from sample accession ERS510129 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510129">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510129</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660927</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039778</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698882" alias="SC_EXP_14847_8#64" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698882</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#64</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039790, constructed from sample accession ERS510130 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510130">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510130</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660928</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039790</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698883" alias="SC_EXP_14847_8#65" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698883</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#65</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039707, constructed from sample accession ERS510131 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510131">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510131</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660929</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039707</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_8#66" center_name="The Wellcome Trust Sanger Institute" accession="ERX698884">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698884</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_8#66</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_8#66</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039719, constructed from sample accession ERS510132 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510132" refname="SC_MFY5867602-sc-2002477" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510132</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660930</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867602-sc-2002477</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039719</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698885" alias="SC_EXP_14847_8#67" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698885</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039731, constructed from sample accession ERS510133 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510133">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510133</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660931</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039731</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698886" alias="SC_EXP_14847_8#68" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698886</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039743, constructed from sample accession ERS510134 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510134">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510134</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660932</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039743</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698887" alias="SC_EXP_14847_8#69" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698887</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#69</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039755, constructed from sample accession ERS510135 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510135">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510135</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660933</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039755</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698888" alias="SC_EXP_14847_8#70" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698888</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#70</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039767, constructed from sample accession ERS510136 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510136">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510136</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660934</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039767</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698889" alias="SC_EXP_14847_8#71" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698889</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#71</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039779, constructed from sample accession ERS510137 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence GTGTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510137">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510137</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660935</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039779</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698890" alias="SC_EXP_14847_8#72" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698890</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#72</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039791, constructed from sample accession ERS510138 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence GACGGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510138">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510138</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660936</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039791</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#71" center_name="The Wellcome Trust Sanger Institute" accession="ERX698699">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698699</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#71</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#71</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056797, constructed from sample accession ERS540785 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence GTGTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540785" refname="SC_MFY5867799-sc-2002535" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540785</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752188</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867799-sc-2002535</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056797</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#72" center_name="The Wellcome Trust Sanger Institute" accession="ERX698700">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698700</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#72</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#72</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056809, constructed from sample accession ERS540786 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence GACGGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540786" refname="SC_MFY5867888-sc-2002536" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540786</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752189</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867888-sc-2002536</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056809</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#73" center_name="The Wellcome Trust Sanger Institute" accession="ERX698701">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698701</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#73</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#73</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056726, constructed from sample accession ERS540787 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540787" refname="SC_MFY5867889-sc-2002538" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540787</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752190</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867889-sc-2002538</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056726</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#74" center_name="The Wellcome Trust Sanger Institute" accession="ERX698702">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698702</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#74</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056738, constructed from sample accession ERS540788 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540788" refname="SC_MFY5867800-sc-2002539" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540788</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752191</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867800-sc-2002539</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056738</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#75" center_name="The Wellcome Trust Sanger Institute" accession="ERX698703">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698703</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#75</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056750, constructed from sample accession ERS540790 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence GAATCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540790" refname="SC_MFY5867890-sc-2002542" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540790</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752193</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867890-sc-2002542</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056750</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#76" center_name="The Wellcome Trust Sanger Institute" accession="ERX698704">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698704</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#76</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056762, constructed from sample accession ERS540789 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540789" refname="SC_MFY5867801-sc-2002541" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540789</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752192</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867801-sc-2002541</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056762</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#77" center_name="The Wellcome Trust Sanger Institute" accession="ERX698705">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698705</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#77</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056774, constructed from sample accession ERS540791 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540791" refname="SC_MFY5867891-sc-2002544" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540791</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752194</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867891-sc-2002544</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056774</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#78" center_name="The Wellcome Trust Sanger Institute" accession="ERX698706">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698706</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#78</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#78</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056786, constructed from sample accession ERS540792 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540792" refname="SC_MFY5867802-sc-2002545" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540792</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752195</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867802-sc-2002545</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056786</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#79" center_name="The Wellcome Trust Sanger Institute" accession="ERX698707">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698707</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#79</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056798, constructed from sample accession ERS540794 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540794" refname="SC_MFY5867803-sc-2002547" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540794</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752197</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867803-sc-2002547</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056798</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#80" center_name="The Wellcome Trust Sanger Institute" accession="ERX698708">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698708</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#80</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056810, constructed from sample accession ERS540793 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence GTCGCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540793" refname="SC_MFY5867892-sc-2002546" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540793</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752196</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867892-sc-2002546</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056810</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#81" center_name="The Wellcome Trust Sanger Institute" accession="ERX698709">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698709</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#81</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056727, constructed from sample accession ERS540795 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540795" refname="SC_MFY5867804-sc-2002548" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540795</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752198</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867804-sc-2002548</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056727</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#82" center_name="The Wellcome Trust Sanger Institute" accession="ERX698710">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698710</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#82</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#82</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056739, constructed from sample accession ERS540796 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540796" refname="SC_MFY5867893-sc-2002549" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540796</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752199</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867893-sc-2002549</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056739</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </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="ERX698891" alias="SC_EXP_14847_8#73" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698891</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#73</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039708, constructed from sample accession ERS510139 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510139">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510139</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660937</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039708</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698892" alias="SC_EXP_14847_8#74" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698892</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039720, constructed from sample accession ERS510140 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510140">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510140</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660938</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039720</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698893" alias="SC_EXP_14847_8#75" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698893</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039732, constructed from sample accession ERS510141 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence GAATCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510141">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510141</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660939</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039732</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698894" alias="SC_EXP_14847_8#76" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698894</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039744, constructed from sample accession ERS510142 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510142">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510142</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660940</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039744</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698895" alias="SC_EXP_14847_8#77" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698895</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039756, constructed from sample accession ERS510143 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510143">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510143</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660941</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039756</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698896" alias="SC_EXP_14847_8#78" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698896</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#78</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039768, constructed from sample accession ERS510144 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510144">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510144</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660942</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039768</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698897" alias="SC_EXP_14847_8#79" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698897</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039780, constructed from sample accession ERS510145 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510145">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510145</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660943</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039780</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698898" alias="SC_EXP_14847_8#80" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698898</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039792, constructed from sample accession ERS510147 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence GTCGCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510147">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510147</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660945</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039792</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698899" alias="SC_EXP_14847_8#81" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698899</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039709, constructed from sample accession ERS510146 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510146">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510146</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660944</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039709</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698900" alias="SC_EXP_14847_8#82" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698900</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#82</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039721, constructed from sample accession ERS510148 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510148">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510148</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660946</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039721</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698901" alias="SC_EXP_14847_8#83" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698901</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#83</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039733, constructed from sample accession ERS510149 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence GCTCCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510149">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510149</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660947</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039733</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698902" alias="SC_EXP_14847_8#84" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698902</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#84</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039745, constructed from sample accession ERS510150 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence GTAAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510150">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510150</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660948</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039745</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#83" center_name="The Wellcome Trust Sanger Institute" accession="ERX698711">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698711</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#83</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#83</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056751, constructed from sample accession ERS540797 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence GCTCCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540797" refname="SC_MFY5867894-sc-2002550" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752200</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867894-sc-2002550</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056751</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#84" center_name="The Wellcome Trust Sanger Institute" accession="ERX698712">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698712</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#84</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#84</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056763, constructed from sample accession ERS540798 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence GTAAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540798" refname="SC_MFY5867805-sc-2002551" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540798</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752201</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867805-sc-2002551</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056763</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#85" center_name="The Wellcome Trust Sanger Institute" accession="ERX698713">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698713</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#85</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#85</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056775, constructed from sample accession ERS540799 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence GAGGATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540799" refname="SC_MFY5867895-sc-2002552" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540799</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752202</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867895-sc-2002552</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056775</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#86" center_name="The Wellcome Trust Sanger Institute" accession="ERX698714">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698714</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#86</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056787, constructed from sample accession ERS540800 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence GTTGTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540800" refname="SC_MFY5867896-sc-2002553" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540800</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752203</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867896-sc-2002553</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056787</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#87" center_name="The Wellcome Trust Sanger Institute" accession="ERX698715">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698715</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#87</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056799, constructed from sample accession ERS540801 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence GGATTAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540801" refname="SC_MFY5867897-sc-2002554" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540801</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752204</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867897-sc-2002554</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056799</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#88" center_name="The Wellcome Trust Sanger Institute" accession="ERX698716">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698716</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#88</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#88</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056811, constructed from sample accession ERS540802 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence GATAGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540802" refname="SC_MFY5867898-sc-2002555" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540802</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752205</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867898-sc-2002555</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056811</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#89" center_name="The Wellcome Trust Sanger Institute" accession="ERX698717">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698717</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#89</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#89</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056728, constructed from sample accession ERS540803 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence GTGTGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540803" refname="SC_MFY5867899-sc-2002556" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540803</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752206</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867899-sc-2002556</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056728</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#90" center_name="The Wellcome Trust Sanger Institute" accession="ERX698718">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698718</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#90</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#90</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056740, constructed from sample accession ERS540804 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence GCAATCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540804" refname="SC_MFY5867900-sc-2002557" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540804</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752207</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867900-sc-2002557</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056740</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#91" center_name="The Wellcome Trust Sanger Institute" accession="ERX698719">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698719</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#91</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#91</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056752, constructed from sample accession ERS540805 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence GACCTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540805" refname="SC_MFY5867901-sc-2002558" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540805</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752208</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867901-sc-2002558</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056752</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#92" center_name="The Wellcome Trust Sanger Institute" accession="ERX698720">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698720</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#92</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#92</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056764, constructed from sample accession ERS540516 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence GCCTGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540516" refname="SC_MFY5867902-sc-2002559" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540516</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2751919</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867902-sc-2002559</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056764</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#93" center_name="The Wellcome Trust Sanger Institute" accession="ERX698721">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698721</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#93</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#93</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056776, constructed from sample accession ERS540517 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence GCACTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540517" refname="SC_MFY5867903-sc-2002560" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540517</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2751920</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867903-sc-2002560</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056776</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#94" center_name="The Wellcome Trust Sanger Institute" accession="ERX698722">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698722</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#94</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#94</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056788, constructed from sample accession ERS540518 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence GCTAACTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540518" refname="SC_MFY5867904-sc-2002561" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540518</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2751921</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867904-sc-2002561</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056788</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </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="ERX698903" alias="SC_EXP_14847_8#85" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698903</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#85</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039757, constructed from sample accession ERS510151 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence GAGGATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510151">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510151</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660949</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039757</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698904" alias="SC_EXP_14847_8#86" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698904</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039769, constructed from sample accession ERS510152 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence GTTGTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510152">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510152</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660950</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039769</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698905" alias="SC_EXP_14847_8#87" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698905</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039781, constructed from sample accession ERS510153 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence GGATTAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510153">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510153</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660951</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039781</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698906" alias="SC_EXP_14847_8#88" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698906</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#88</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039793, constructed from sample accession ERS510154 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence GATAGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510154">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510154</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660952</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039793</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698907" alias="SC_EXP_14847_8#89" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698907</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#89</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039710, constructed from sample accession ERS510155 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence GTGTGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510155">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510155</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660953</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039710</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698908" alias="SC_EXP_14847_8#90" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698908</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#90</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039722, constructed from sample accession ERS510156 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence GCAATCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510156">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510156</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660954</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039722</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698909" alias="SC_EXP_14847_8#91" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698909</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#91</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039734, constructed from sample accession ERS510157 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence GACCTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510157">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510157</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660955</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039734</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698910" alias="SC_EXP_14847_8#92" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698910</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#92</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039746, constructed from sample accession ERS510158 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence GCCTGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510158">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510158</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660956</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039746</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698911" alias="SC_EXP_14847_8#93" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698911</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#93</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039758, constructed from sample accession ERS510159 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence GCACTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510159">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510159</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660957</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039758</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_8#94" center_name="The Wellcome Trust Sanger Institute" accession="ERX698912">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698912</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_8#94</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_8#94</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039770, constructed from sample accession ERS540614 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence GCTAACTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540614" refname="SC_MFY5867710-sc-2002185" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540614</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752017</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867710-sc-2002185</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039770</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_8#95" center_name="The Wellcome Trust Sanger Institute" accession="ERX698913">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698913</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_8#95</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_8#95</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039782, constructed from sample accession ERS540615 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence GATTCATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540615" refname="SC_MFY5867711-sc-2002188" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540615</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752018</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867711-sc-2002188</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039782</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#95" center_name="The Wellcome Trust Sanger Institute" accession="ERX698723">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698723</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#95</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#95</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056800, constructed from sample accession ERS540519 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence GATTCATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540519" refname="SC_MFY5867905-sc-2002562" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540519</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2751922</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867905-sc-2002562</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056800</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#1" center_name="The Wellcome Trust Sanger Institute" accession="ERX698724">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698724</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056426, constructed from sample accession ERS540616 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540616" refname="SC_MFY5867712-sc-2002191" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540616</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752019</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867712-sc-2002191</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056426</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#2" center_name="The Wellcome Trust Sanger Institute" accession="ERX698725">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698725</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056438, constructed from sample accession ERS540617 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540617" refname="SC_MFY5867713-sc-2002195" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540617</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752020</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867713-sc-2002195</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056438</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#3" center_name="The Wellcome Trust Sanger Institute" accession="ERX698726">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698726</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056450, constructed from sample accession ERS540619 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540619" refname="SC_MFY5867806-sc-2002201" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540619</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752022</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867806-sc-2002201</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056450</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#4" center_name="The Wellcome Trust Sanger Institute" accession="ERX698727">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698727</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056462, constructed from sample accession ERS540620 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540620" refname="SC_MFY5867715-sc-2002202" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540620</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752023</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867715-sc-2002202</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056462</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#5" center_name="The Wellcome Trust Sanger Institute" accession="ERX698728">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698728</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056474, constructed from sample accession ERS540622 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540622" refname="SC_MFY5867716-sc-2002206" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540622</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752025</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867716-sc-2002206</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056474</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#6" center_name="The Wellcome Trust Sanger Institute" accession="ERX698729">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698729</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056486, constructed from sample accession ERS540621 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540621" refname="SC_MFY5867807-sc-2002205" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540621</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752024</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867807-sc-2002205</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056486</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#7" center_name="The Wellcome Trust Sanger Institute" accession="ERX698730">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698730</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056498, constructed from sample accession ERS540623 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540623" refname="SC_MFY5867717-sc-2002209" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540623</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752026</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867717-sc-2002209</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056498</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX698731">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698731</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056510, constructed from sample accession ERS540624 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540624" refname="SC_MFY5867808-sc-2002211" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540624</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752027</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867808-sc-2002211</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056510</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#9" center_name="The Wellcome Trust Sanger Institute" accession="ERX698732">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698732</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056427, constructed from sample accession ERS540625 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540625" refname="SC_MFY5867718-sc-2002213" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540625</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752028</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867718-sc-2002213</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056427</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#10" center_name="The Wellcome Trust Sanger Institute" accession="ERX698733">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698733</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056439, constructed from sample accession ERS540626 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540626" refname="SC_MFY5867809-sc-2002215" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540626</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752029</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867809-sc-2002215</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056439</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#11" center_name="The Wellcome Trust Sanger Institute" accession="ERX698734">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698734</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056451, constructed from sample accession ERS540627 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540627" refname="SC_MFY5867719-sc-2002217" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540627</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752030</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867719-sc-2002217</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056451</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#12" center_name="The Wellcome Trust Sanger Institute" accession="ERX698735">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698735</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056463, constructed from sample accession ERS540628 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540628" refname="SC_MFY5867810-sc-2002218" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540628</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752031</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867810-sc-2002218</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056463</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#13" center_name="The Wellcome Trust Sanger Institute" accession="ERX698736">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698736</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056475, constructed from sample accession ERS540629 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540629" refname="SC_MFY5867720-sc-2002221" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540629</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752032</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867720-sc-2002221</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056475</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#14" center_name="The Wellcome Trust Sanger Institute" accession="ERX698737">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698737</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056487, constructed from sample accession ERS540630 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540630" refname="SC_MFY5867811-sc-2002223" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540630</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752033</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867811-sc-2002223</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056487</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#15" center_name="The Wellcome Trust Sanger Institute" accession="ERX698738">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698738</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056499, constructed from sample accession ERS540631 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540631" refname="SC_MFY5867721-sc-2002225" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540631</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752034</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867721-sc-2002225</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056499</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#16" center_name="The Wellcome Trust Sanger Institute" accession="ERX698739">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698739</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056511, constructed from sample accession ERS540632 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540632" refname="SC_MFY5867812-sc-2002227" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540632</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752035</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867812-sc-2002227</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056511</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#17" center_name="The Wellcome Trust Sanger Institute" accession="ERX698740">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698740</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056428, constructed from sample accession ERS540633 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540633" refname="SC_MFY5867722-sc-2002229" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540633</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752036</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867722-sc-2002229</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056428</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#18" center_name="The Wellcome Trust Sanger Institute" accession="ERX698741">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698741</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056440, constructed from sample accession ERS540634 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540634" refname="SC_MFY5867813-sc-2002232" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540634</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752037</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867813-sc-2002232</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056440</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#19" center_name="The Wellcome Trust Sanger Institute" accession="ERX698742">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698742</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056452, constructed from sample accession ERS540636 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540636" refname="SC_MFY5867814-sc-2002236" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540636</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752039</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867814-sc-2002236</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056452</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#20" center_name="The Wellcome Trust Sanger Institute" accession="ERX698743">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698743</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056464, constructed from sample accession ERS540637 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540637" refname="SC_MFY5867724-sc-2002237" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540637</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752040</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867724-sc-2002237</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056464</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#21" center_name="The Wellcome Trust Sanger Institute" accession="ERX698744">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698744</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056476, constructed from sample accession ERS540638 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540638" refname="SC_MFY5867815-sc-2002240" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540638</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752041</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867815-sc-2002240</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056476</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#22" center_name="The Wellcome Trust Sanger Institute" accession="ERX698745">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698745</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056488, constructed from sample accession ERS540639 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540639" refname="SC_MFY5867725-sc-2002241" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540639</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752042</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867725-sc-2002241</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056488</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#23" center_name="The Wellcome Trust Sanger Institute" accession="ERX698746">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698746</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056500, constructed from sample accession ERS540640 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540640" refname="SC_MFY5867816-sc-2002245" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540640</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752043</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867816-sc-2002245</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056500</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#24" center_name="The Wellcome Trust Sanger Institute" accession="ERX698747">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698747</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056512, constructed from sample accession ERS540641 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540641" refname="SC_MFY5867726-sc-2002246" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540641</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752044</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867726-sc-2002246</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056512</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#25" center_name="The Wellcome Trust Sanger Institute" accession="ERX698748">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698748</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056429, constructed from sample accession ERS540642 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540642" refname="SC_MFY5867727-sc-2002248" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540642</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752045</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867727-sc-2002248</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056429</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#26" center_name="The Wellcome Trust Sanger Institute" accession="ERX698749">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698749</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056441, constructed from sample accession ERS540643 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540643" refname="SC_MFY5867817-sc-2002250" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540643</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752046</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867817-sc-2002250</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056441</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#27" center_name="The Wellcome Trust Sanger Institute" accession="ERX698750">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698750</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056453, constructed from sample accession ERS540644 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540644" refname="SC_MFY5867728-sc-2002253" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540644</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752047</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867728-sc-2002253</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056453</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#28" center_name="The Wellcome Trust Sanger Institute" accession="ERX698751">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698751</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056465, constructed from sample accession ERS540645 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540645" refname="SC_MFY5867818-sc-2002255" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540645</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752048</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867818-sc-2002255</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056465</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#29" center_name="The Wellcome Trust Sanger Institute" accession="ERX698752">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698752</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056477, constructed from sample accession ERS540646 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540646" refname="SC_MFY5867729-sc-2002256" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540646</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752049</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867729-sc-2002256</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056477</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#30" center_name="The Wellcome Trust Sanger Institute" accession="ERX698753">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698753</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056489, constructed from sample accession ERS540647 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540647" refname="SC_MFY5867819-sc-2002259" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540647</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752050</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867819-sc-2002259</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056489</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX698754">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698754</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056501, constructed from sample accession ERS540649 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540649" refname="SC_MFY5867820-sc-2002263" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540649</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752052</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867820-sc-2002263</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056501</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX698755">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698755</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056513, constructed from sample accession ERS540650 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540650" refname="SC_MFY5867731-sc-2002264" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540650</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752053</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867731-sc-2002264</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056513</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX698756">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698756</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056430, constructed from sample accession ERS540651 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540651" refname="SC_MFY5867821-sc-2002267" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540651</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752054</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867821-sc-2002267</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056430</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX698757">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698757</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056442, constructed from sample accession ERS540652 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540652" refname="SC_MFY5867732-sc-2002268" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540652</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752055</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867732-sc-2002268</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056442</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX698758">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698758</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056454, constructed from sample accession ERS540653 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540653" refname="SC_MFY5867822-sc-2002271" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540653</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752056</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867822-sc-2002271</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056454</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX698759">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698759</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056466, constructed from sample accession ERS540654 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540654" refname="SC_MFY5867733-sc-2002272" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540654</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752057</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867733-sc-2002272</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056466</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX698760">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698760</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056478, constructed from sample accession ERS540655 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540655" refname="SC_MFY5867823-sc-2002274" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540655</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752058</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867823-sc-2002274</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056478</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX698761">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698761</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056490, constructed from sample accession ERS540656 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540656" refname="SC_MFY5867734-sc-2002276" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540656</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752059</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867734-sc-2002276</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056490</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#39" center_name="The Wellcome Trust Sanger Institute" accession="ERX698762">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698762</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#39</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056502, constructed from sample accession ERS540657 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540657" refname="SC_MFY5867824-sc-2002278" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540657</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752060</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867824-sc-2002278</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056502</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#40" center_name="The Wellcome Trust Sanger Institute" accession="ERX698763">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698763</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#40</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056514, constructed from sample accession ERS540658 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540658" refname="SC_MFY5867735-sc-2002280" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540658</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752061</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867735-sc-2002280</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056514</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#41" center_name="The Wellcome Trust Sanger Institute" accession="ERX698764">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698764</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#41</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056431, constructed from sample accession ERS540659 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540659" refname="SC_MFY5867825-sc-2002282" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540659</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752062</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867825-sc-2002282</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056431</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#42" center_name="The Wellcome Trust Sanger Institute" accession="ERX698765">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698765</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#42</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056443, constructed from sample accession ERS540660 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540660" refname="SC_MFY5867736-sc-2002284" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540660</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752063</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867736-sc-2002284</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056443</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#43" center_name="The Wellcome Trust Sanger Institute" accession="ERX698766">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698766</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#43</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056455, constructed from sample accession ERS540661 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540661" refname="SC_MFY5867826-sc-2002286" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540661</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752064</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867826-sc-2002286</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056455</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#44" center_name="The Wellcome Trust Sanger Institute" accession="ERX698767">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698767</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#44</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056467, constructed from sample accession ERS540662 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540662" refname="SC_MFY5867737-sc-2002288" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540662</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752065</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867737-sc-2002288</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056467</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#45" center_name="The Wellcome Trust Sanger Institute" accession="ERX698768">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698768</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#45</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056479, constructed from sample accession ERS540663 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540663" refname="SC_MFY5867827-sc-2002290" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540663</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752066</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867827-sc-2002290</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056479</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#46" center_name="The Wellcome Trust Sanger Institute" accession="ERX698769">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698769</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#46</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056491, constructed from sample accession ERS540664 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540664" refname="SC_MFY5867738-sc-2002292" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540664</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752067</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867738-sc-2002292</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056491</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#47" center_name="The Wellcome Trust Sanger Institute" accession="ERX698770">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698770</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#47</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056503, constructed from sample accession ERS540665 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540665" refname="SC_MFY5867828-sc-2002294" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540665</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752068</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867828-sc-2002294</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056503</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#48" center_name="The Wellcome Trust Sanger Institute" accession="ERX698771">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698771</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#48</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056515, constructed from sample accession ERS540666 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540666" refname="SC_MFY5867739-sc-2002297" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540666</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752069</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867739-sc-2002297</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056515</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#49" center_name="The Wellcome Trust Sanger Institute" accession="ERX698772">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698772</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#49</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056432, constructed from sample accession ERS540667 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540667" refname="SC_MFY5867829-sc-2002298" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540667</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752070</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867829-sc-2002298</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056432</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#50" center_name="The Wellcome Trust Sanger Institute" accession="ERX698773">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698773</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#50</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056444, constructed from sample accession ERS540668 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540668" refname="SC_MFY5867740-sc-2002301" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540668</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752071</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867740-sc-2002301</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056444</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#51" center_name="The Wellcome Trust Sanger Institute" accession="ERX698774">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698774</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#51</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056456, constructed from sample accession ERS540669 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540669" refname="SC_MFY5867830-sc-2002302" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540669</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752072</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867830-sc-2002302</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056456</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#52" center_name="The Wellcome Trust Sanger Institute" accession="ERX698775">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698775</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#52</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056468, constructed from sample accession ERS540670 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540670" refname="SC_MFY5867741-sc-2002305" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540670</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752073</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867741-sc-2002305</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056468</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#53" center_name="The Wellcome Trust Sanger Institute" accession="ERX698776">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698776</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#53</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056480, constructed from sample accession ERS540671 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540671" refname="SC_MFY5867831-sc-2002307" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540671</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752074</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867831-sc-2002307</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056480</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#54" center_name="The Wellcome Trust Sanger Institute" accession="ERX698777">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698777</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#54</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056492, constructed from sample accession ERS540672 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540672" refname="SC_MFY5867742-sc-2002309" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540672</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752075</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867742-sc-2002309</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056492</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#55" center_name="The Wellcome Trust Sanger Institute" accession="ERX698778">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698778</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#55</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056504, constructed from sample accession ERS540673 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540673" refname="SC_MFY5867832-sc-2002312" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540673</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752076</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867832-sc-2002312</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056504</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#56" center_name="The Wellcome Trust Sanger Institute" accession="ERX698779">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698779</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#56</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056516, constructed from sample accession ERS540674 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540674" refname="SC_MFY5867743-sc-2002313" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540674</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752077</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867743-sc-2002313</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056516</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#57" center_name="The Wellcome Trust Sanger Institute" accession="ERX698780">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698780</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#57</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056433, constructed from sample accession ERS540675 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540675" refname="SC_MFY5867833-sc-2002316" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540675</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752078</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867833-sc-2002316</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056433</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#58" center_name="The Wellcome Trust Sanger Institute" accession="ERX698781">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698781</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#58</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056445, constructed from sample accession ERS540676 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540676" refname="SC_MFY5867744-sc-2002318" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540676</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752079</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867744-sc-2002318</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056445</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#59" center_name="The Wellcome Trust Sanger Institute" accession="ERX698782">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698782</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#59</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056457, constructed from sample accession ERS540677 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540677" refname="SC_MFY5867834-sc-2002320" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540677</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752080</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867834-sc-2002320</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056457</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#60" center_name="The Wellcome Trust Sanger Institute" accession="ERX698783">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698783</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#60</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#60</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056469, constructed from sample accession ERS540678 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540678" refname="SC_MFY5867745-sc-2002321" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540678</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752081</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867745-sc-2002321</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056469</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#61" center_name="The Wellcome Trust Sanger Institute" accession="ERX698784">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698784</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#61</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056481, constructed from sample accession ERS540679 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540679" refname="SC_MFY5867835-sc-2002324" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540679</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752082</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867835-sc-2002324</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056481</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#62" center_name="The Wellcome Trust Sanger Institute" accession="ERX698785">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698785</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#62</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056493, constructed from sample accession ERS540680 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540680" refname="SC_MFY5867746-sc-2002325" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540680</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752083</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867746-sc-2002325</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056493</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#63" center_name="The Wellcome Trust Sanger Institute" accession="ERX698786">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698786</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#63</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#63</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056505, constructed from sample accession ERS540681 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540681" refname="SC_MFY5867836-sc-2002328" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540681</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752084</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867836-sc-2002328</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056505</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#64" center_name="The Wellcome Trust Sanger Institute" accession="ERX698787">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698787</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#64</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#64</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056517, constructed from sample accession ERS540682 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540682" refname="SC_MFY5867747-sc-2002330" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540682</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752085</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867747-sc-2002330</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056517</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#65" center_name="The Wellcome Trust Sanger Institute" accession="ERX698788">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698788</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#65</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#65</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056434, constructed from sample accession ERS540683 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540683" refname="SC_MFY5867837-sc-2002332" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540683</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752086</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867837-sc-2002332</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056434</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#66" center_name="The Wellcome Trust Sanger Institute" accession="ERX698789">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698789</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#66</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#66</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056446, constructed from sample accession ERS540684 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540684" refname="SC_MFY5867748-sc-2002334" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540684</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752087</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867748-sc-2002334</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056446</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#67" center_name="The Wellcome Trust Sanger Institute" accession="ERX698790">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698790</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#67</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056458, constructed from sample accession ERS540685 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540685" refname="SC_MFY5867838-sc-2002336" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540685</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752088</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867838-sc-2002336</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056458</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#68" center_name="The Wellcome Trust Sanger Institute" accession="ERX698791">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698791</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#68</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056470, constructed from sample accession ERS540686 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540686" refname="SC_MFY5867749-sc-2002337" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540686</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752089</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867749-sc-2002337</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056470</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#69" center_name="The Wellcome Trust Sanger Institute" accession="ERX698792">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698792</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#69</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#69</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056482, constructed from sample accession ERS540687 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540687" refname="SC_MFY5867839-sc-2002339" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540687</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752090</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867839-sc-2002339</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056482</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#70" center_name="The Wellcome Trust Sanger Institute" accession="ERX698793">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698793</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#70</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#70</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056494, constructed from sample accession ERS540688 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540688" refname="SC_MFY5867750-sc-2002340" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540688</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752091</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867750-sc-2002340</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056494</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#71" center_name="The Wellcome Trust Sanger Institute" accession="ERX698794">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698794</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#71</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#71</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056506, constructed from sample accession ERS540690 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence GTGTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540690" refname="SC_MFY5867751-sc-2002345" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540690</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752093</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867751-sc-2002345</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056506</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#72" center_name="The Wellcome Trust Sanger Institute" accession="ERX698795">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698795</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#72</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#72</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056518, constructed from sample accession ERS540689 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence GACGGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540689" refname="SC_MFY5867840-sc-2002343" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540689</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752092</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867840-sc-2002343</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056518</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#73" center_name="The Wellcome Trust Sanger Institute" accession="ERX698796">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698796</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#73</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#73</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056435, constructed from sample accession ERS540691 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540691" refname="SC_MFY5867752-sc-2002347" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540691</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752094</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867752-sc-2002347</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056435</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#74" center_name="The Wellcome Trust Sanger Institute" accession="ERX698797">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698797</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#74</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056447, constructed from sample accession ERS540692 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540692" refname="SC_MFY5867841-sc-2002348" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540692</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752095</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867841-sc-2002348</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056447</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#75" center_name="The Wellcome Trust Sanger Institute" accession="ERX698798">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698798</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#75</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056459, constructed from sample accession ERS540693 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence GAATCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540693" refname="SC_MFY5867753-sc-2002350" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540693</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752096</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867753-sc-2002350</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056459</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#76" center_name="The Wellcome Trust Sanger Institute" accession="ERX698799">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698799</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#76</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056471, constructed from sample accession ERS540694 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540694" refname="SC_MFY5867842-sc-2002351" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540694</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752097</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867842-sc-2002351</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056471</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#77" center_name="The Wellcome Trust Sanger Institute" accession="ERX698800">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698800</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#77</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056483, constructed from sample accession ERS540695 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540695" refname="SC_MFY5867754-sc-2002353" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540695</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752098</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867754-sc-2002353</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056483</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#78" center_name="The Wellcome Trust Sanger Institute" accession="ERX698801">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698801</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#78</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#78</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056495, constructed from sample accession ERS540696 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540696" refname="SC_MFY5867843-sc-2002354" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540696</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752099</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867843-sc-2002354</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056495</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#79" center_name="The Wellcome Trust Sanger Institute" accession="ERX698802">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698802</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#79</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056507, constructed from sample accession ERS540697 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540697" refname="SC_MFY5867755-sc-2002357" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540697</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752100</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867755-sc-2002357</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056507</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#80" center_name="The Wellcome Trust Sanger Institute" accession="ERX698803">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698803</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#80</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056519, constructed from sample accession ERS540698 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence GTCGCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540698" refname="SC_MFY5867844-sc-2002358" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540698</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752101</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867844-sc-2002358</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056519</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#81" center_name="The Wellcome Trust Sanger Institute" accession="ERX698804">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698804</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#81</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056436, constructed from sample accession ERS540699 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540699" refname="SC_MFY5867756-sc-2002362" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540699</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752102</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867756-sc-2002362</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056436</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#82" center_name="The Wellcome Trust Sanger Institute" accession="ERX698805">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698805</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#82</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#82</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056448, constructed from sample accession ERS540700 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540700" refname="SC_MFY5867845-sc-2002363" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540700</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752103</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867845-sc-2002363</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056448</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#83" center_name="The Wellcome Trust Sanger Institute" accession="ERX698806">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698806</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#83</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#83</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056460, constructed from sample accession ERS540701 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence GCTCCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540701" refname="SC_MFY5867757-sc-2002366" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540701</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752104</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867757-sc-2002366</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056460</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#84" center_name="The Wellcome Trust Sanger Institute" accession="ERX698807">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698807</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#84</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#84</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056472, constructed from sample accession ERS540702 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence GTAAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540702" refname="SC_MFY5867846-sc-2002367" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540702</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752105</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867846-sc-2002367</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056472</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#85" center_name="The Wellcome Trust Sanger Institute" accession="ERX698808">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698808</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#85</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#85</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056484, constructed from sample accession ERS540703 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence GAGGATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540703" refname="SC_MFY5867758-sc-2002370" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540703</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752106</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867758-sc-2002370</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056484</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#86" center_name="The Wellcome Trust Sanger Institute" accession="ERX698809">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698809</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#86</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056496, constructed from sample accession ERS540704 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence GTTGTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540704" refname="SC_MFY5867847-sc-2002373" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540704</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752107</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867847-sc-2002373</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056496</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#87" center_name="The Wellcome Trust Sanger Institute" accession="ERX698810">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698810</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#87</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056508, constructed from sample accession ERS540705 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence GGATTAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540705" refname="SC_MFY5867759-sc-2002374" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540705</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752108</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867759-sc-2002374</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056508</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#88" center_name="The Wellcome Trust Sanger Institute" accession="ERX698811">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698811</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#88</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#88</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056520, constructed from sample accession ERS540706 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence GATAGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540706" refname="SC_MFY5867848-sc-2002377" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540706</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752109</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867848-sc-2002377</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056520</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#89" center_name="The Wellcome Trust Sanger Institute" accession="ERX698812">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698812</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#89</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#89</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056437, constructed from sample accession ERS540707 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence GTGTGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540707" refname="SC_MFY5867760-sc-2002379" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540707</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752110</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867760-sc-2002379</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056437</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#90" center_name="The Wellcome Trust Sanger Institute" accession="ERX698813">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698813</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#90</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#90</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056449, constructed from sample accession ERS540708 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence GCAATCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540708" refname="SC_MFY5867849-sc-2002381" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540708</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752111</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867849-sc-2002381</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056449</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#91" center_name="The Wellcome Trust Sanger Institute" accession="ERX698814">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698814</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#91</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#91</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056461, constructed from sample accession ERS540709 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence GACCTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540709" refname="SC_MFY5867761-sc-2002384" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540709</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752112</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867761-sc-2002384</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056461</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#92" center_name="The Wellcome Trust Sanger Institute" accession="ERX698815">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698815</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#92</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#92</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056473, constructed from sample accession ERS540710 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence GCCTGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540710" refname="SC_MFY5867850-sc-2002386" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540710</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752113</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867850-sc-2002386</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056473</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#93" center_name="The Wellcome Trust Sanger Institute" accession="ERX698816">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698816</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#93</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#93</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056485, constructed from sample accession ERS540712 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence GCACTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540712" refname="SC_MFY5867851-sc-2002390" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540712</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752115</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867851-sc-2002390</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056485</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#94" center_name="The Wellcome Trust Sanger Institute" accession="ERX698817">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698817</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#94</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#94</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056497, constructed from sample accession ERS540713 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence GCTAACTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540713" refname="SC_MFY5867763-sc-2002393" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540713</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752116</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867763-sc-2002393</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056497</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_7#95" center_name="The Wellcome Trust Sanger Institute" accession="ERX698818">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698818</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_7#95</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_7#95</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056509, constructed from sample accession ERS540714 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_7).  This submission includes reads tagged with the sequence GATTCATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540714" refname="SC_MFY5867852-sc-2002395" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540714</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752117</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867852-sc-2002395</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056509</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="259" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#1" center_name="The Wellcome Trust Sanger Institute" accession="ERX698629">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698629</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056717, constructed from sample accession ERS540715 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540715" refname="SC_MFY5867764-sc-2002398" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540715</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752118</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867764-sc-2002398</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056717</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#2" center_name="The Wellcome Trust Sanger Institute" accession="ERX698630">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698630</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056729, constructed from sample accession ERS540716 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540716" refname="SC_MFY5867853-sc-2002399" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540716</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752119</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867853-sc-2002399</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056729</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#3" center_name="The Wellcome Trust Sanger Institute" accession="ERX698631">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698631</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056741, constructed from sample accession ERS540717 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540717" refname="SC_MFY5867765-sc-2002402" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540717</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752120</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867765-sc-2002402</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056741</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#4" center_name="The Wellcome Trust Sanger Institute" accession="ERX698632">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698632</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056753, constructed from sample accession ERS540718 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540718" refname="SC_MFY5867854-sc-2002405" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540718</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752121</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867854-sc-2002405</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056753</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#5" center_name="The Wellcome Trust Sanger Institute" accession="ERX698633">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698633</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056765, constructed from sample accession ERS540719 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540719" refname="SC_MFY5867766-sc-2002406" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540719</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752122</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867766-sc-2002406</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056765</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#6" center_name="The Wellcome Trust Sanger Institute" accession="ERX698634">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698634</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056777, constructed from sample accession ERS540721 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540721" refname="SC_MFY5867767-sc-2002410" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540721</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752124</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867767-sc-2002410</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056777</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#7" center_name="The Wellcome Trust Sanger Institute" accession="ERX698635">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698635</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056789, constructed from sample accession ERS540720 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540720" refname="SC_MFY5867855-sc-2002409" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540720</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752123</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867855-sc-2002409</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056789</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX698636">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698636</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056801, constructed from sample accession ERS540722 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540722" refname="SC_MFY5867768-sc-2002413" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540722</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752125</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867768-sc-2002413</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056801</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#9" center_name="The Wellcome Trust Sanger Institute" accession="ERX698637">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698637</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056718, constructed from sample accession ERS540723 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540723" refname="SC_MFY5867856-sc-2002414" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540723</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752126</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867856-sc-2002414</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056718</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#10" center_name="The Wellcome Trust Sanger Institute" accession="ERX698638">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698638</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056730, constructed from sample accession ERS540724 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540724" refname="SC_MFY5867769-sc-2002417" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540724</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752127</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867769-sc-2002417</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056730</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </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="ERX698819" alias="SC_EXP_14847_8#1" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698819</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039699, constructed from sample accession ERS510067 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510067">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510067</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660865</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039699</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698820" alias="SC_EXP_14847_8#2" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698820</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039711, constructed from sample accession ERS510068 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510068">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510068</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660866</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039711</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698821" alias="SC_EXP_14847_8#3" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698821</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039723, constructed from sample accession ERS510069 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510069">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510069</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660867</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039723</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698822" alias="SC_EXP_14847_8#4" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698822</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039735, constructed from sample accession ERS510070 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510070">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510070</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660868</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039735</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698823" alias="SC_EXP_14847_8#5" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698823</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039747, constructed from sample accession ERS510071 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510071">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510071</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660869</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039747</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698824" alias="SC_EXP_14847_8#6" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698824</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039759, constructed from sample accession ERS510072 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510072">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510072</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660870</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039759</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698825" alias="SC_EXP_14847_8#7" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698825</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039771, constructed from sample accession ERS510073 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510073">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510073</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660871</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039771</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698826" alias="SC_EXP_14847_8#8" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698826</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039783, constructed from sample accession ERS510074 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510074">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510074</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660872</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039783</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698827" alias="SC_EXP_14847_8#9" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698827</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039700, constructed from sample accession ERS510075 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510075">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510075</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660873</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039700</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698828" alias="SC_EXP_14847_8#10" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698828</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039712, constructed from sample accession ERS510076 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510076">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510076</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660874</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039712</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_8#11" center_name="The Wellcome Trust Sanger Institute" accession="ERX698829">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698829</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_8#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_8#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039724, constructed from sample accession ERS510077 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510077" refname="SC_MFY5867574-sc-2002372" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510077</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660875</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867574-sc-2002372</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039724</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698830" alias="SC_EXP_14847_8#12" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698830</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039736, constructed from sample accession ERS510078 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510078">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510078</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660876</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039736</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#11" center_name="The Wellcome Trust Sanger Institute" accession="ERX698639">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698639</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056742, constructed from sample accession ERS540725 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540725" refname="SC_MFY5867857-sc-2002418" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540725</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752128</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867857-sc-2002418</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056742</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#12" center_name="The Wellcome Trust Sanger Institute" accession="ERX698640">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698640</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056754, constructed from sample accession ERS540726 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540726" refname="SC_MFY5867770-sc-2002421" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540726</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752129</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867770-sc-2002421</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056754</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#13" center_name="The Wellcome Trust Sanger Institute" accession="ERX698641">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698641</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056766, constructed from sample accession ERS540727 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540727" refname="SC_MFY5867858-sc-2002422" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540727</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752130</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867858-sc-2002422</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056766</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#14" center_name="The Wellcome Trust Sanger Institute" accession="ERX698642">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698642</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056778, constructed from sample accession ERS540728 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540728" refname="SC_MFY5867771-sc-2002425" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540728</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752131</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867771-sc-2002425</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056778</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#15" center_name="The Wellcome Trust Sanger Institute" accession="ERX698643">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698643</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056790, constructed from sample accession ERS540729 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540729" refname="SC_MFY5867859-sc-2002426" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540729</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752132</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867859-sc-2002426</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056790</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#16" center_name="The Wellcome Trust Sanger Institute" accession="ERX698644">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698644</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056802, constructed from sample accession ERS540730 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540730" refname="SC_MFY5867772-sc-2002429" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540730</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752133</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867772-sc-2002429</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056802</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#17" center_name="The Wellcome Trust Sanger Institute" accession="ERX698645">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698645</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056719, constructed from sample accession ERS540731 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540731" refname="SC_MFY5867860-sc-2002430" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540731</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752134</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867860-sc-2002430</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056719</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#18" center_name="The Wellcome Trust Sanger Institute" accession="ERX698646">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698646</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056731, constructed from sample accession ERS540732 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540732" refname="SC_MFY5867773-sc-2002433" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540732</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752135</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867773-sc-2002433</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056731</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#19" center_name="The Wellcome Trust Sanger Institute" accession="ERX698647">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698647</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056743, constructed from sample accession ERS540733 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540733" refname="SC_MFY5867861-sc-2002434" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540733</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752136</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867861-sc-2002434</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056743</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#20" center_name="The Wellcome Trust Sanger Institute" accession="ERX698648">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698648</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056755, constructed from sample accession ERS540734 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540734" refname="SC_MFY5867774-sc-2002437" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540734</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752137</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867774-sc-2002437</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056755</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#21" center_name="The Wellcome Trust Sanger Institute" accession="ERX698649">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698649</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056767, constructed from sample accession ERS540735 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540735" refname="SC_MFY5867862-sc-2002439" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540735</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752138</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867862-sc-2002439</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056767</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#22" center_name="The Wellcome Trust Sanger Institute" accession="ERX698650">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698650</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056779, constructed from sample accession ERS540736 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540736" refname="SC_MFY5867775-sc-2002441" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540736</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752139</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867775-sc-2002441</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056779</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </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="ERX698831" alias="SC_EXP_14847_8#13" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698831</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039748, constructed from sample accession ERS510079 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510079">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510079</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660877</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039748</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698832" alias="SC_EXP_14847_8#14" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698832</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039760, constructed from sample accession ERS510080 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510080">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510080</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660878</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039760</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698833" alias="SC_EXP_14847_8#15" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698833</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039772, constructed from sample accession ERS510081 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510081">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510081</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660879</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039772</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698834" alias="SC_EXP_14847_8#16" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698834</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039784, constructed from sample accession ERS510082 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510082">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510082</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660880</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039784</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698835" alias="SC_EXP_14847_8#17" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698835</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039701, constructed from sample accession ERS510083 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510083">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510083</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660881</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039701</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698836" alias="SC_EXP_14847_8#18" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698836</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039713, constructed from sample accession ERS510084 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510084">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510084</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660882</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039713</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698837" alias="SC_EXP_14847_8#19" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698837</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039725, constructed from sample accession ERS510085 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510085">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510085</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660883</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039725</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698838" alias="SC_EXP_14847_8#20" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698838</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039737, constructed from sample accession ERS510086 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510086">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510086</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660884</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039737</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698839" alias="SC_EXP_14847_8#21" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698839</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039749, constructed from sample accession ERS510087 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510087">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510087</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660885</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039749</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698840" alias="SC_EXP_14847_8#22" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698840</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039761, constructed from sample accession ERS510088 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510088">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510088</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660886</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039761</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698841" alias="SC_EXP_14847_8#23" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698841</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039773, constructed from sample accession ERS510089 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510089">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510089</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660887</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039773</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698842" alias="SC_EXP_14847_8#24" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698842</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039785, constructed from sample accession ERS510091 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510091">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510091</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660889</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039785</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#23" center_name="The Wellcome Trust Sanger Institute" accession="ERX698651">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698651</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056791, constructed from sample accession ERS540737 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540737" refname="SC_MFY5867863-sc-2002442" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540737</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752140</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867863-sc-2002442</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056791</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#24" center_name="The Wellcome Trust Sanger Institute" accession="ERX698652">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698652</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056803, constructed from sample accession ERS540738 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540738" refname="SC_MFY5867776-sc-2002445" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540738</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752141</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867776-sc-2002445</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056803</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#25" center_name="The Wellcome Trust Sanger Institute" accession="ERX698653">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698653</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056720, constructed from sample accession ERS540739 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540739" refname="SC_MFY5867864-sc-2002447" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540739</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752142</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867864-sc-2002447</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056720</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#26" center_name="The Wellcome Trust Sanger Institute" accession="ERX698654">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698654</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056732, constructed from sample accession ERS540740 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540740" refname="SC_MFY5867777-sc-2002449" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540740</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752143</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867777-sc-2002449</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056732</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#27" center_name="The Wellcome Trust Sanger Institute" accession="ERX698655">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698655</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056744, constructed from sample accession ERS540741 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540741" refname="SC_MFY5867865-sc-2002451" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540741</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752144</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867865-sc-2002451</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056744</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#28" center_name="The Wellcome Trust Sanger Institute" accession="ERX698656">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698656</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056756, constructed from sample accession ERS540742 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540742" refname="SC_MFY5867778-sc-2002454" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540742</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752145</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867778-sc-2002454</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056756</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#29" center_name="The Wellcome Trust Sanger Institute" accession="ERX698657">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698657</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056768, constructed from sample accession ERS540743 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540743" refname="SC_MFY5867866-sc-2002455" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540743</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752146</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867866-sc-2002455</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056768</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#30" center_name="The Wellcome Trust Sanger Institute" accession="ERX698658">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698658</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056780, constructed from sample accession ERS540744 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540744" refname="SC_MFY5867779-sc-2002458" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540744</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752147</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867779-sc-2002458</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056780</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX698659">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698659</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056792, constructed from sample accession ERS540745 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540745" refname="SC_MFY5867867-sc-2002459" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540745</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752148</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867867-sc-2002459</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056792</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX698660">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698660</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056804, constructed from sample accession ERS540746 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540746" refname="SC_MFY5867780-sc-2002462" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540746</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752149</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867780-sc-2002462</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056804</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX698661">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698661</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056721, constructed from sample accession ERS540747 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540747" refname="SC_MFY5867868-sc-2002463" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540747</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752150</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867868-sc-2002463</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056721</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX698662">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698662</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056733, constructed from sample accession ERS540748 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540748" refname="SC_MFY5867869-sc-2002466" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540748</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752151</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867869-sc-2002466</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056733</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </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="ERX698843" alias="SC_EXP_14847_8#25" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698843</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039702, constructed from sample accession ERS510090 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510090">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510090</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660888</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039702</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698844" alias="SC_EXP_14847_8#26" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698844</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039714, constructed from sample accession ERS510092 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510092">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510092</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660890</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039714</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698845" alias="SC_EXP_14847_8#27" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698845</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039726, constructed from sample accession ERS510093 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510093">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510093</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660891</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039726</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698846" alias="SC_EXP_14847_8#28" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698846</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039738, constructed from sample accession ERS510094 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510094">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510094</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660892</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039738</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_8#29" center_name="The Wellcome Trust Sanger Institute" accession="ERX698847">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698847</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_8#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_8#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039750, constructed from sample accession ERS510095 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510095" refname="SC_MFY5867582-sc-2002404" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510095</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867582-sc-2002404</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039750</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698848" alias="SC_EXP_14847_8#30" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698848</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039762, constructed from sample accession ERS510096 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510096">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510096</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660894</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039762</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698849" alias="SC_EXP_14847_8#31" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698849</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039774, constructed from sample accession ERS510097 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510097">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510097</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660895</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039774</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698850" alias="SC_EXP_14847_8#32" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698850</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039786, constructed from sample accession ERS510098 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510098">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510098</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660896</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039786</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698851" alias="SC_EXP_14847_8#33" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698851</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039703, constructed from sample accession ERS510099 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510099">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510099</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660897</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039703</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698852" alias="SC_EXP_14847_8#34" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698852</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039715, constructed from sample accession ERS510101 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510101">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510101</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660899</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039715</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698853" alias="SC_EXP_14847_8#35" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698853</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039727, constructed from sample accession ERS510100 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510100">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510100</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660898</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039727</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698854" alias="SC_EXP_14847_8#36" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698854</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039739, constructed from sample accession ERS510102 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510102">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510102</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660900</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039739</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX698663">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698663</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056745, constructed from sample accession ERS540749 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540749" refname="SC_MFY5867781-sc-2002467" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540749</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752152</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867781-sc-2002467</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056745</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX698664">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698664</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056757, constructed from sample accession ERS540750 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540750" refname="SC_MFY5867870-sc-2002470" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540750</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752153</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867870-sc-2002470</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056757</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX698665">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698665</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056769, constructed from sample accession ERS540751 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540751" refname="SC_MFY5867782-sc-2002472" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540751</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752154</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867782-sc-2002472</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056769</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX698666">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698666</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056781, constructed from sample accession ERS540752 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540752" refname="SC_MFY5867871-sc-2002475" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540752</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752155</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867871-sc-2002475</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056781</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#39" center_name="The Wellcome Trust Sanger Institute" accession="ERX698667">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698667</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#39</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056793, constructed from sample accession ERS540753 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540753" refname="SC_MFY5867783-sc-2002476" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540753</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752156</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867783-sc-2002476</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056793</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#40" center_name="The Wellcome Trust Sanger Institute" accession="ERX698668">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698668</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#40</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056805, constructed from sample accession ERS540754 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540754" refname="SC_MFY5867872-sc-2002479" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540754</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752157</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867872-sc-2002479</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056805</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#41" center_name="The Wellcome Trust Sanger Institute" accession="ERX698669">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698669</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#41</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056722, constructed from sample accession ERS540755 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540755" refname="SC_MFY5867784-sc-2002480" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540755</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752158</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867784-sc-2002480</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056722</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#42" center_name="The Wellcome Trust Sanger Institute" accession="ERX698670">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698670</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#42</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056734, constructed from sample accession ERS540756 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540756" refname="SC_MFY5867873-sc-2002482" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540756</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752159</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867873-sc-2002482</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056734</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#43" center_name="The Wellcome Trust Sanger Institute" accession="ERX698671">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698671</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#43</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056746, constructed from sample accession ERS540757 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540757" refname="SC_MFY5867785-sc-2002484" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540757</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752160</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867785-sc-2002484</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056746</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#44" center_name="The Wellcome Trust Sanger Institute" accession="ERX698672">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698672</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#44</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056758, constructed from sample accession ERS540758 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540758" refname="SC_MFY5867874-sc-2002486" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540758</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752161</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867874-sc-2002486</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056758</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#45" center_name="The Wellcome Trust Sanger Institute" accession="ERX698673">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698673</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#45</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056770, constructed from sample accession ERS540759 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540759" refname="SC_MFY5867786-sc-2002489" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540759</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752162</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867786-sc-2002489</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056770</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_6#46" center_name="The Wellcome Trust Sanger Institute" accession="ERX698674">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698674</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_6#46</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_6#46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12056782, constructed from sample accession ERS540760 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_6).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS540760" refname="SC_MFY5867875-sc-2002490" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS540760</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2752163</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867875-sc-2002490</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12056782</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="105"/>
        </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="ERX698855" alias="SC_EXP_14847_8#37" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698855</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039751, constructed from sample accession ERS510103 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510103">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510103</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660901</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039751</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698856" alias="SC_EXP_14847_8#38" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698856</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039763, constructed from sample accession ERS510104 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510104">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510104</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660902</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039763</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698857" alias="SC_EXP_14847_8#39" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698857</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039775, constructed from sample accession ERS510105 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510105">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510105</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660903</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039775</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698858" alias="SC_EXP_14847_8#40" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698858</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039787, constructed from sample accession ERS510106 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510106">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510106</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660904</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039787</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698859" alias="SC_EXP_14847_8#41" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698859</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039704, constructed from sample accession ERS510107 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510107">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510107</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660905</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039704</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698860" alias="SC_EXP_14847_8#42" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698860</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039716, constructed from sample accession ERS510108 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510108">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510108</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660906</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039716</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698861" alias="SC_EXP_14847_8#43" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698861</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039728, constructed from sample accession ERS510109 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510109">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510109</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660907</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039728</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14847_8#44" center_name="The Wellcome Trust Sanger Institute" accession="ERX698862">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698862</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14847_8#44</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14847_8#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001366" refname="Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001366</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identification_of_mutational_spectra_in_fission_yeast_DNA_repair_and_chromatin_mutants__S_cerevisiae_-sc-2012-04-17T16:20:27Z-2197</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039740, constructed from sample accession ERS510110 for study accession ERP001366.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510110" refname="SC_MFY5867590-sc-2002435" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510110</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660908</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_MFY5867590-sc-2002435</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039740</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698863" alias="SC_EXP_14847_8#45" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698863</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039752, constructed from sample accession ERS510111 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510111">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510111</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660909</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039752</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698864" alias="SC_EXP_14847_8#46" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698864</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039764, constructed from sample accession ERS510112 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510112">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510112</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660910</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039764</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698865" alias="SC_EXP_14847_8#47" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698865</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039776, constructed from sample accession ERS510113 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510113">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510113</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660911</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039776</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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="ERX698866" alias="SC_EXP_14847_8#48" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX698866</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_14847_8#48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP127302">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP127302</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB43347</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12039788, constructed from sample accession ERS510114 for study accession ERP127302.  This is part of an Illumina multiplexed sequencing run (14847_8).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS510114">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS510114</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2660912</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12039788</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="266" NOMINAL_SDEV="109"/>
        </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>
