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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="SC_EXP_13510_2#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX589703">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589703</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13510_2#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13510_2#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262137, constructed from sample accession ERS434652 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13510_2).  This submission includes reads tagged with the sequence TACTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434652" refname="SC_Ape25766820-sc-1886235" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434652</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464846</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766820-sc-1886235</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262137</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="475" NOMINAL_SDEV="51"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13510_2#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX589704">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589704</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13510_2#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13510_2#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262149, constructed from sample accession ERS434653 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13510_2).  This submission includes reads tagged with the sequence TCTCACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434653" refname="SC_Ape25766821-sc-1886236" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434653</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464847</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766821-sc-1886236</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262149</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="475" NOMINAL_SDEV="51"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13511_1#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX589705">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589705</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13511_1#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13511_1#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262160, constructed from sample accession ERS434646 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13511_1).  This submission includes reads tagged with the sequence TAGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434646" refname="SC_Ape25766814-sc-1886229" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434646</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464840</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766814-sc-1886229</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262160</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="477" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13511_1#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX589706">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589706</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13511_1#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13511_1#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262172, constructed from sample accession ERS434647 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13511_1).  This submission includes reads tagged with the sequence TTCCATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434647" refname="SC_Ape25766815-sc-1886230" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434647</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464841</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766815-sc-1886230</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262172</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="477" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13511_1#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX589707">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589707</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13511_1#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13511_1#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262089, constructed from sample accession ERS434648 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13511_1).  This submission includes reads tagged with the sequence TCGAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434648" refname="SC_Ape25766816-sc-1886231" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434648</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464842</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766816-sc-1886231</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262089</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="477" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13511_1#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX589708">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589708</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13511_1#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13511_1#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262101, constructed from sample accession ERS434649 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13511_1).  This submission includes reads tagged with the sequence TAACGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434649" refname="SC_Ape25766817-sc-1886232" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434649</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464843</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766817-sc-1886232</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262101</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="477" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13511_1#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX589709">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589709</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13511_1#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13511_1#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262113, constructed from sample accession ERS434650 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13511_1).  This submission includes reads tagged with the sequence TTGGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434650" refname="SC_Ape25766818-sc-1886233" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434650</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464844</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766818-sc-1886233</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262113</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="477" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13511_1#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX589710">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589710</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13511_1#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13511_1#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262125, constructed from sample accession ERS434651 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13511_1).  This submission includes reads tagged with the sequence TGAACTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434651" refname="SC_Ape25766819-sc-1886234" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434651</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464845</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766819-sc-1886234</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262125</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="477" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13511_1#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX589711">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589711</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13511_1#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13511_1#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262137, constructed from sample accession ERS434652 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13511_1).  This submission includes reads tagged with the sequence TACTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434652" refname="SC_Ape25766820-sc-1886235" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434652</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464846</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766820-sc-1886235</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262137</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="477" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13511_1#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX589712">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589712</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13511_1#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13511_1#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262149, constructed from sample accession ERS434653 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13511_1).  This submission includes reads tagged with the sequence TCTCACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434653" refname="SC_Ape25766821-sc-1886236" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434653</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464847</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766821-sc-1886236</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262149</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="477" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13511_2#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX589713">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589713</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13511_2#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13511_2#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262160, constructed from sample accession ERS434646 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13511_2).  This submission includes reads tagged with the sequence TAGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434646" refname="SC_Ape25766814-sc-1886229" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434646</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464840</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766814-sc-1886229</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262160</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="476" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13511_2#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX589714">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589714</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13511_2#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13511_2#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262172, constructed from sample accession ERS434647 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13511_2).  This submission includes reads tagged with the sequence TTCCATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434647" refname="SC_Ape25766815-sc-1886230" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434647</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464841</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766815-sc-1886230</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262172</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="476" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13511_2#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX589715">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589715</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13511_2#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13511_2#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262089, constructed from sample accession ERS434648 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13511_2).  This submission includes reads tagged with the sequence TCGAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434648" refname="SC_Ape25766816-sc-1886231" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434648</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464842</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766816-sc-1886231</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262089</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="476" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13511_2#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX589716">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589716</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13511_2#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13511_2#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262101, constructed from sample accession ERS434649 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13511_2).  This submission includes reads tagged with the sequence TAACGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434649" refname="SC_Ape25766817-sc-1886232" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434649</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464843</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766817-sc-1886232</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262101</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="476" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13511_2#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX589717">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589717</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13511_2#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13511_2#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262113, constructed from sample accession ERS434650 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13511_2).  This submission includes reads tagged with the sequence TTGGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434650" refname="SC_Ape25766818-sc-1886233" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434650</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464844</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766818-sc-1886233</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262113</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="476" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13511_2#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX589718">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589718</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13511_2#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13511_2#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262125, constructed from sample accession ERS434651 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13511_2).  This submission includes reads tagged with the sequence TGAACTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434651" refname="SC_Ape25766819-sc-1886234" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434651</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464845</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766819-sc-1886234</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262125</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="476" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13511_2#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX589719">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589719</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13511_2#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13511_2#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262137, constructed from sample accession ERS434652 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13511_2).  This submission includes reads tagged with the sequence TACTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434652" refname="SC_Ape25766820-sc-1886235" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434652</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464846</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766820-sc-1886235</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262137</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="476" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13511_2#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX589720">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589720</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13511_2#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13511_2#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262149, constructed from sample accession ERS434653 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13511_2).  This submission includes reads tagged with the sequence TCTCACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434653" refname="SC_Ape25766821-sc-1886236" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434653</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464847</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766821-sc-1886236</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262149</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="476" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13509_1#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX589673">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589673</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13509_1#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13509_1#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262160, constructed from sample accession ERS434646 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13509_1).  This submission includes reads tagged with the sequence TAGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434646" refname="SC_Ape25766814-sc-1886229" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434646</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464840</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766814-sc-1886229</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262160</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="476" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13509_1#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX589674">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589674</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13509_1#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13509_1#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262172, constructed from sample accession ERS434647 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13509_1).  This submission includes reads tagged with the sequence TTCCATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434647" refname="SC_Ape25766815-sc-1886230" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434647</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464841</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766815-sc-1886230</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262172</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="476" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13509_1#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX589675">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589675</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13509_1#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13509_1#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262089, constructed from sample accession ERS434648 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13509_1).  This submission includes reads tagged with the sequence TCGAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434648" refname="SC_Ape25766816-sc-1886231" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434648</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464842</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766816-sc-1886231</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262089</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="476" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13509_1#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX589676">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589676</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13509_1#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13509_1#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262101, constructed from sample accession ERS434649 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13509_1).  This submission includes reads tagged with the sequence TAACGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434649" refname="SC_Ape25766817-sc-1886232" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434649</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464843</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766817-sc-1886232</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262101</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="476" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13509_1#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX589677">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589677</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13509_1#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13509_1#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262113, constructed from sample accession ERS434650 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13509_1).  This submission includes reads tagged with the sequence TTGGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434650" refname="SC_Ape25766818-sc-1886233" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434650</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464844</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766818-sc-1886233</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262113</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="476" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13509_1#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX589678">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589678</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13509_1#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13509_1#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262125, constructed from sample accession ERS434651 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13509_1).  This submission includes reads tagged with the sequence TGAACTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434651" refname="SC_Ape25766819-sc-1886234" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434651</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464845</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766819-sc-1886234</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262125</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="476" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13509_1#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX589679">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589679</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13509_1#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13509_1#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262137, constructed from sample accession ERS434652 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13509_1).  This submission includes reads tagged with the sequence TACTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434652" refname="SC_Ape25766820-sc-1886235" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434652</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464846</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766820-sc-1886235</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262137</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="476" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13509_1#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX589680">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589680</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13509_1#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13509_1#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262149, constructed from sample accession ERS434653 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13509_1).  This submission includes reads tagged with the sequence TCTCACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434653" refname="SC_Ape25766821-sc-1886236" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434653</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464847</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766821-sc-1886236</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262149</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="476" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13509_2#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX589681">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589681</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13509_2#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13509_2#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262160, constructed from sample accession ERS434646 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13509_2).  This submission includes reads tagged with the sequence TAGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434646" refname="SC_Ape25766814-sc-1886229" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434646</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464840</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766814-sc-1886229</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262160</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="477" NOMINAL_SDEV="53"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13509_2#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX589682">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589682</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13509_2#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13509_2#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262172, constructed from sample accession ERS434647 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13509_2).  This submission includes reads tagged with the sequence TTCCATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434647" refname="SC_Ape25766815-sc-1886230" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434647</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464841</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766815-sc-1886230</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262172</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="477" NOMINAL_SDEV="53"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13509_2#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX589683">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589683</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13509_2#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13509_2#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262089, constructed from sample accession ERS434648 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13509_2).  This submission includes reads tagged with the sequence TCGAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434648" refname="SC_Ape25766816-sc-1886231" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434648</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464842</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766816-sc-1886231</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262089</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="477" NOMINAL_SDEV="53"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13509_2#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX589684">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589684</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13509_2#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13509_2#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262101, constructed from sample accession ERS434649 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13509_2).  This submission includes reads tagged with the sequence TAACGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434649" refname="SC_Ape25766817-sc-1886232" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434649</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464843</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766817-sc-1886232</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262101</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="477" NOMINAL_SDEV="53"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13509_2#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX589685">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589685</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13509_2#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13509_2#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262113, constructed from sample accession ERS434650 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13509_2).  This submission includes reads tagged with the sequence TTGGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434650" refname="SC_Ape25766818-sc-1886233" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434650</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464844</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766818-sc-1886233</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262113</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="477" NOMINAL_SDEV="53"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13509_2#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX589686">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589686</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13509_2#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13509_2#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262125, constructed from sample accession ERS434651 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13509_2).  This submission includes reads tagged with the sequence TGAACTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434651" refname="SC_Ape25766819-sc-1886234" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434651</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464845</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766819-sc-1886234</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262125</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="477" NOMINAL_SDEV="53"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13509_2#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX589687">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589687</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13509_2#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13509_2#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262137, constructed from sample accession ERS434652 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13509_2).  This submission includes reads tagged with the sequence TACTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434652" refname="SC_Ape25766820-sc-1886235" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434652</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464846</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766820-sc-1886235</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262137</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="477" NOMINAL_SDEV="53"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13509_2#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX589688">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589688</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13509_2#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13509_2#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262149, constructed from sample accession ERS434653 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13509_2).  This submission includes reads tagged with the sequence TCTCACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434653" refname="SC_Ape25766821-sc-1886236" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434653</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464847</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766821-sc-1886236</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262149</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="477" NOMINAL_SDEV="53"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13510_1#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX589689">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589689</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13510_1#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13510_1#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262160, constructed from sample accession ERS434646 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13510_1).  This submission includes reads tagged with the sequence TAGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434646" refname="SC_Ape25766814-sc-1886229" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434646</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464840</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766814-sc-1886229</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262160</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="475" NOMINAL_SDEV="50"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13510_1#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX589690">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589690</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13510_1#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13510_1#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262172, constructed from sample accession ERS434647 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13510_1).  This submission includes reads tagged with the sequence TTCCATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434647" refname="SC_Ape25766815-sc-1886230" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434647</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464841</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766815-sc-1886230</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262172</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="475" NOMINAL_SDEV="50"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13510_1#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX589691">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589691</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13510_1#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13510_1#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262089, constructed from sample accession ERS434648 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13510_1).  This submission includes reads tagged with the sequence TCGAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434648" refname="SC_Ape25766816-sc-1886231" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434648</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464842</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766816-sc-1886231</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262089</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="475" NOMINAL_SDEV="50"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13510_1#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX589692">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589692</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13510_1#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13510_1#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262101, constructed from sample accession ERS434649 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13510_1).  This submission includes reads tagged with the sequence TAACGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434649" refname="SC_Ape25766817-sc-1886232" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434649</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464843</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766817-sc-1886232</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262101</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="475" NOMINAL_SDEV="50"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13510_1#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX589693">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589693</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13510_1#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13510_1#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262113, constructed from sample accession ERS434650 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13510_1).  This submission includes reads tagged with the sequence TTGGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434650" refname="SC_Ape25766818-sc-1886233" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434650</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464844</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766818-sc-1886233</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262113</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="475" NOMINAL_SDEV="50"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13510_1#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX589694">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589694</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13510_1#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13510_1#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262125, constructed from sample accession ERS434651 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13510_1).  This submission includes reads tagged with the sequence TGAACTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434651" refname="SC_Ape25766819-sc-1886234" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434651</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464845</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766819-sc-1886234</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262125</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="475" NOMINAL_SDEV="50"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13510_1#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX589695">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589695</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13510_1#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13510_1#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262137, constructed from sample accession ERS434652 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13510_1).  This submission includes reads tagged with the sequence TACTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434652" refname="SC_Ape25766820-sc-1886235" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434652</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464846</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766820-sc-1886235</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262137</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="475" NOMINAL_SDEV="50"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13510_1#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX589696">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589696</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13510_1#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13510_1#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262149, constructed from sample accession ERS434653 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13510_1).  This submission includes reads tagged with the sequence TCTCACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434653" refname="SC_Ape25766821-sc-1886236" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434653</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464847</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766821-sc-1886236</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262149</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="475" NOMINAL_SDEV="50"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13510_2#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX589697">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589697</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13510_2#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13510_2#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262160, constructed from sample accession ERS434646 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13510_2).  This submission includes reads tagged with the sequence TAGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434646" refname="SC_Ape25766814-sc-1886229" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434646</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464840</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766814-sc-1886229</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262160</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="475" NOMINAL_SDEV="51"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13510_2#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX589698">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589698</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13510_2#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13510_2#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262172, constructed from sample accession ERS434647 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13510_2).  This submission includes reads tagged with the sequence TTCCATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434647" refname="SC_Ape25766815-sc-1886230" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434647</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464841</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766815-sc-1886230</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262172</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="475" NOMINAL_SDEV="51"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13510_2#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX589699">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589699</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13510_2#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13510_2#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262089, constructed from sample accession ERS434648 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13510_2).  This submission includes reads tagged with the sequence TCGAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434648" refname="SC_Ape25766816-sc-1886231" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434648</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464842</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766816-sc-1886231</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262089</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="475" NOMINAL_SDEV="51"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13510_2#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX589700">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589700</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13510_2#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13510_2#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262101, constructed from sample accession ERS434649 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13510_2).  This submission includes reads tagged with the sequence TAACGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434649" refname="SC_Ape25766817-sc-1886232" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434649</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464843</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766817-sc-1886232</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262101</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="475" NOMINAL_SDEV="51"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13510_2#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX589701">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589701</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13510_2#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13510_2#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262113, constructed from sample accession ERS434650 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13510_2).  This submission includes reads tagged with the sequence TTGGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434650" refname="SC_Ape25766818-sc-1886233" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434650</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464844</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766818-sc-1886233</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262113</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="475" NOMINAL_SDEV="51"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13510_2#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX589702">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX589702</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13510_2#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13510_2#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005359" refname="GreatApeGenomes2-sc-3008" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005359</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">GreatApeGenomes2-sc-3008</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10262125, constructed from sample accession ERS434651 for study accession ERP005359.  This is part of an Illumina multiplexed sequencing run (13510_2).  This submission includes reads tagged with the sequence TGAACTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS434651" refname="SC_Ape25766819-sc-1886234" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS434651</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2464845</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">SC_Ape25766819-sc-1886234</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10262125</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="475" NOMINAL_SDEV="51"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
