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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
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      <PRIMARY_ID>ERX553470</PRIMARY_ID>
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      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13296_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>
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      </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 (13296_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>
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      </LIBRARY_DESCRIPTOR>
    </DESIGN>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13296_2#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX553471">
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      <PRIMARY_ID>ERX553471</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13296_2#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13296_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>
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      </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 (13296_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>
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          <PAIRED NOMINAL_LENGTH="476" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13296_2#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX553472">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553472</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13296_2#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13296_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 (13296_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_13296_2#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX553473">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553473</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13296_2#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13296_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 (13296_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_13296_2#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX553474">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553474</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13296_2#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13296_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 (13296_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_13296_2#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX553475">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553475</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13296_2#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13296_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 (13296_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_13295_1#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX553446">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553446</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13295_1#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13295_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 (13295_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="51"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
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      <PRIMARY_ID>ERX553447</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13295_1#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13295_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 (13295_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>
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        <LIBRARY_NAME>10262089</LIBRARY_NAME>
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        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="476" NOMINAL_SDEV="51"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
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      <PRIMARY_ID>ERX553448</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13295_1#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13295_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>
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    <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 (13295_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>
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        <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="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_13295_1#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX553449">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553449</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13295_1#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13295_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 (13295_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="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_13295_1#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX553450">
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      <PRIMARY_ID>ERX553450</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13295_1#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13295_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 (13295_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="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_13295_1#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX553451">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553451</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13295_1#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13295_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 (13295_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="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_13295_1#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX553452">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553452</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13295_1#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13295_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 (13295_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="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_13295_2#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX553453">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553453</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13295_2#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13295_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 (13295_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="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_13295_2#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX553454">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553454</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13295_2#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13295_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 (13295_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="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_13295_2#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX553455">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553455</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13295_2#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13295_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 (13295_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="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_13295_2#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX553456">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553456</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13295_2#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13295_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 (13295_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="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_13295_2#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX553457">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553457</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13295_2#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13295_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 (13295_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="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_13295_2#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX553458">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553458</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13295_2#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13295_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 (13295_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="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_13295_2#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX553459">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553459</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13295_2#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13295_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 (13295_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="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_13295_2#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX553460">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553460</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13295_2#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13295_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 (13295_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="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_13296_1#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX553461">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553461</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13296_1#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13296_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 (13296_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="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_13296_1#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX553462">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553462</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13296_1#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13296_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 (13296_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="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_13296_1#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX553463">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553463</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13296_1#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13296_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 (13296_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="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_13296_1#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX553464">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553464</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13296_1#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13296_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 (13296_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="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_13296_1#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX553465">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553465</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13296_1#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13296_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 (13296_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="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_13296_1#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX553466">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553466</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13296_1#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13296_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 (13296_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="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_13296_1#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX553467">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553467</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13296_1#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13296_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 (13296_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="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_13296_1#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX553468">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553468</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13296_1#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13296_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 (13296_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="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_13296_2#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX553469">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553469</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13296_2#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13296_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 (13296_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_13296_2#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX553476">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553476</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13296_2#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13296_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 (13296_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_13300_1#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX553477">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553477</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13300_1#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13300_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 (13300_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="474" 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_13300_1#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX553478">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553478</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13300_1#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13300_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 (13300_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="474" 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_13300_1#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX553479">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553479</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13300_1#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13300_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 (13300_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="474" 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_13300_1#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX553480">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553480</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13300_1#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13300_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 (13300_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="474" 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_13300_1#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX553481">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553481</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13300_1#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13300_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 (13300_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="474" 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_13300_1#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX553482">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553482</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13300_1#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13300_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 (13300_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="474" 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_13300_1#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX553483">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553483</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13300_1#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13300_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 (13300_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="474" 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_13300_1#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX553484">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553484</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13300_1#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13300_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 (13300_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="474" 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_13300_2#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX553485">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553485</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13300_2#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13300_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 (13300_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="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_13300_2#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX553486">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553486</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13300_2#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13300_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 (13300_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="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_13300_2#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX553487">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553487</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13300_2#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13300_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 (13300_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="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_13300_2#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX553488">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553488</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13300_2#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13300_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 (13300_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="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_13300_2#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX553489">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553489</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13300_2#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13300_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 (13300_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="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_13300_2#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX553490">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553490</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13300_2#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13300_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 (13300_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="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_13300_2#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX553491">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553491</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13300_2#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13300_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 (13300_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="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_13300_2#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX553492">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553492</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13300_2#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13300_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 (13300_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="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_13301_1#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX553493">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553493</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13301_1#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13301_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 (13301_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="474" 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_13301_1#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX553494">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553494</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13301_1#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13301_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 (13301_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="474" 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_13301_1#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX553495">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553495</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13301_1#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13301_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 (13301_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="474" 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_13301_1#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX553496">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553496</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13301_1#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13301_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 (13301_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="474" 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_13301_1#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX553497">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553497</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13301_1#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13301_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 (13301_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="474" 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_13301_1#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX553498">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553498</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13301_1#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13301_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 (13301_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="474" 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_13301_1#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX553499">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553499</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13301_1#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13301_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 (13301_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="474" 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_13301_1#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX553500">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553500</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13301_1#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13301_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 (13301_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="474" 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_13301_2#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX553501">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553501</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13301_2#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13301_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 (13301_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="474" 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_13301_2#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX553502">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553502</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13301_2#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13301_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 (13301_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="474" 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_13301_2#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX553503">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553503</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13301_2#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13301_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 (13301_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="474" 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_13301_2#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX553504">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553504</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13301_2#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13301_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 (13301_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="474" 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_13301_2#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX553505">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553505</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13301_2#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13301_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 (13301_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="474" 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_13301_2#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX553506">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553506</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13301_2#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13301_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 (13301_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="474" 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_13301_2#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX553507">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553507</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13301_2#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13301_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 (13301_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="474" 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_13301_2#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX553508">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553508</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13301_2#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13301_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 (13301_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="474" 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_13312_1#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX553509">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553509</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13312_1#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13312_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 (13312_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_13312_1#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX553510">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553510</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13312_1#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13312_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 (13312_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_13312_1#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX553511">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553511</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13312_1#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13312_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 (13312_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_13312_1#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX553512">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553512</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13312_1#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13312_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 (13312_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_13312_1#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX553513">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553513</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13312_1#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13312_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 (13312_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_13312_1#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX553514">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553514</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13312_1#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13312_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 (13312_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_13312_1#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX553515">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553515</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13312_1#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13312_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 (13312_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_13312_1#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX553516">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553516</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13312_1#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13312_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 (13312_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_13312_2#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX553517">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553517</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13312_2#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13312_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 (13312_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="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_13312_2#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX553518">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553518</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13312_2#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13312_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 (13312_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="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_13312_2#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX553519">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553519</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13312_2#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13312_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 (13312_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="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_13312_2#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX553520">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553520</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13312_2#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13312_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 (13312_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="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_13312_2#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX553521">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553521</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13312_2#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13312_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 (13312_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="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_13312_2#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX553522">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553522</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13312_2#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13312_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 (13312_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="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_13312_2#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX553523">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553523</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13312_2#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13312_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 (13312_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="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_13312_2#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX553524">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553524</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13312_2#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13312_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 (13312_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="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_13313_1#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX553525">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553525</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13313_1#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13313_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 (13313_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="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_13313_1#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX553526">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553526</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13313_1#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13313_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 (13313_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="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_13313_1#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX553527">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553527</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13313_1#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13313_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 (13313_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="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_13313_1#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX553528">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553528</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13313_1#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13313_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 (13313_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="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_13313_1#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX553529">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553529</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13313_1#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13313_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 (13313_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="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_13313_1#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX553530">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553530</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13313_1#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13313_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 (13313_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="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_13313_1#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX553531">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553531</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13313_1#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13313_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 (13313_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="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_13313_1#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX553532">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553532</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13313_1#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13313_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 (13313_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="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_13313_2#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX553533">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553533</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13313_2#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13313_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 (13313_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="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_13313_2#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX553534">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553534</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13313_2#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13313_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 (13313_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="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_13313_2#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX553535">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553535</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13313_2#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13313_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 (13313_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="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_13313_2#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX553536">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553536</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13313_2#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13313_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 (13313_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="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_13313_2#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX553537">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553537</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13313_2#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13313_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 (13313_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="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_13313_2#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX553538">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553538</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13313_2#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13313_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 (13313_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="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_13313_2#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX553539">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553539</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13313_2#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13313_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 (13313_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="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_13313_2#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX553540">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553540</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13313_2#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13313_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 (13313_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="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_13251_1#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX553397">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553397</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13251_1#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13251_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 (13251_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="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_13251_1#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX553398">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553398</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13251_1#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13251_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 (13251_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="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_13251_1#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX553399">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553399</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13251_1#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13251_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 (13251_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="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_13251_1#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX553400">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553400</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13251_1#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13251_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 (13251_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="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_13251_1#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX553401">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553401</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13251_1#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13251_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 (13251_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="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_13251_1#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX553402">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553402</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13251_1#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13251_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 (13251_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="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_13251_1#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX553403">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553403</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13251_1#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13251_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 (13251_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="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_13251_1#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX553404">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553404</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13251_1#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13251_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 (13251_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="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_13251_2#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX553405">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553405</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13251_2#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13251_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 (13251_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="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_13251_2#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX553406">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553406</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13251_2#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13251_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 (13251_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="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_13251_2#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX553407">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553407</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13251_2#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13251_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 (13251_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="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_13251_2#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX553408">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553408</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13251_2#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13251_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 (13251_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="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_13251_2#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX553409">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553409</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13251_2#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13251_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 (13251_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="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_13251_2#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX553410">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553410</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13251_2#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13251_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 (13251_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="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_13251_2#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX553411">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553411</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13251_2#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13251_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 (13251_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="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_13251_2#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX553412">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553412</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13251_2#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13251_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 (13251_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="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_13280_1#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX553413">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553413</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13280_1#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13280_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 (13280_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="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_13280_1#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX553414">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553414</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13280_1#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13280_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 (13280_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="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_13280_1#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX553415">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553415</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13280_1#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13280_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 (13280_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="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_13280_1#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX553416">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553416</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13280_1#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13280_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 (13280_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="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_13280_1#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX553417">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553417</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13280_1#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13280_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 (13280_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="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_13280_1#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX553418">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553418</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13280_1#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13280_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 (13280_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="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_13280_1#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX553419">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553419</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13280_1#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13280_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 (13280_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="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_13280_1#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX553420">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553420</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13280_1#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13280_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 (13280_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="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_13280_2#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX553421">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553421</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13280_2#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13280_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 (13280_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="474" 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_13280_2#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX553422">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553422</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13280_2#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13280_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 (13280_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="474" 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_13280_2#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX553423">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553423</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13280_2#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13280_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 (13280_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="474" 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_13280_2#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX553424">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553424</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13280_2#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13280_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 (13280_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="474" 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_13280_2#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX553425">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553425</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13280_2#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13280_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 (13280_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="474" 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_13280_2#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX553426">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553426</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13280_2#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13280_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 (13280_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="474" 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_13280_2#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX553427">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553427</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13280_2#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13280_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 (13280_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="474" 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_13280_2#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX553428">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553428</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13280_2#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13280_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 (13280_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="474" 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_13281_1#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX553429">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553429</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13281_1#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13281_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 (13281_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_13281_1#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX553430">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553430</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13281_1#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13281_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 (13281_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_13281_1#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX553431">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553431</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13281_1#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13281_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 (13281_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_13281_1#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX553432">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553432</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13281_1#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13281_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 (13281_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_13281_1#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX553433">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553433</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13281_1#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13281_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 (13281_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_13281_1#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX553434">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553434</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13281_1#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13281_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 (13281_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_13281_1#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX553435">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553435</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13281_1#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13281_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 (13281_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_13281_1#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX553436">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553436</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13281_1#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13281_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 (13281_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_13281_2#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX553437">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553437</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13281_2#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13281_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 (13281_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="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_13281_2#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX553438">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553438</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13281_2#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13281_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 (13281_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="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_13281_2#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX553439">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553439</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13281_2#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13281_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 (13281_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="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_13281_2#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX553440">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553440</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13281_2#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13281_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 (13281_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="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_13281_2#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX553441">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553441</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13281_2#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13281_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 (13281_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="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_13281_2#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX553442">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553442</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13281_2#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13281_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 (13281_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="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_13281_2#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX553443">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553443</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13281_2#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13281_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 (13281_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="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_13281_2#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX553444">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553444</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13281_2#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13281_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 (13281_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="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_13295_1#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX553445">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX553445</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13295_1#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13295_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 (13295_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="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>
