<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="SC_EXP_15378_3#48" center_name="The Wellcome Trust Sanger Institute" accession="ERX942051">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942051</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#48</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815475, constructed from sample accession ERS625474 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625474" refname="GPS_MW_1058-sc-2139645" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625474</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1058-sc-2139645</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815475</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#49" center_name="The Wellcome Trust Sanger Institute" accession="ERX942052">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942052</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#49</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815392, constructed from sample accession ERS625475 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625475" refname="GPS_MW_580-sc-2139646" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625475</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_580-sc-2139646</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815392</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#50" center_name="The Wellcome Trust Sanger Institute" accession="ERX942053">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942053</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#50</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815404, constructed from sample accession ERS625476 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625476" refname="GPS_MW_1993-sc-2139647" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625476</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1993-sc-2139647</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815404</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#51" center_name="The Wellcome Trust Sanger Institute" accession="ERX942054">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942054</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#51</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815416, constructed from sample accession ERS625477 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625477" refname="GPS_MW_1742-sc-2139648" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625477</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1742-sc-2139648</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815416</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#52" center_name="The Wellcome Trust Sanger Institute" accession="ERX942055">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942055</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#52</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815428, constructed from sample accession ERS625478 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625478" refname="GPS_MW_2843-sc-2139649" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625478</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2843-sc-2139649</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815428</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#53" center_name="The Wellcome Trust Sanger Institute" accession="ERX942056">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942056</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#53</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815440, constructed from sample accession ERS625479 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625479" refname="GPS_MW_1355-sc-2139650" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625479</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1355-sc-2139650</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815440</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#54" center_name="The Wellcome Trust Sanger Institute" accession="ERX942057">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942057</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#54</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815452, constructed from sample accession ERS625480 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625480" refname="GPS_MW_964-sc-2139652" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625480</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_964-sc-2139652</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815452</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#55" center_name="The Wellcome Trust Sanger Institute" accession="ERX942058">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942058</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#55</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815464, constructed from sample accession ERS625481 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625481" refname="GPS_MW_2399-sc-2139653" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625481</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2399-sc-2139653</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815464</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#56" center_name="The Wellcome Trust Sanger Institute" accession="ERX942059">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942059</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#56</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815476, constructed from sample accession ERS625482 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625482" refname="GPS_MW_784-sc-2139654" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625482</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_784-sc-2139654</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815476</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#57" center_name="The Wellcome Trust Sanger Institute" accession="ERX942060">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942060</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#57</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815393, constructed from sample accession ERS625483 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625483" refname="GPS_MW_1147-sc-2139655" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625483</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1147-sc-2139655</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815393</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#58" center_name="The Wellcome Trust Sanger Institute" accession="ERX942061">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942061</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#58</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815405, constructed from sample accession ERS625484 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625484" refname="GPS_MW_2359-sc-2139656" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625484</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2359-sc-2139656</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815405</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#60" center_name="The Wellcome Trust Sanger Institute" accession="ERX942063">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942063</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#60</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#60</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815429, constructed from sample accession ERS625486 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625486" refname="GPS_MW_1427-sc-2139658" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625486</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1427-sc-2139658</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815429</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#61" center_name="The Wellcome Trust Sanger Institute" accession="ERX942064">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942064</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#61</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815441, constructed from sample accession ERS625487 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625487" refname="GPS_MW_1408-sc-2139659" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625487</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1408-sc-2139659</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815441</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#62" center_name="The Wellcome Trust Sanger Institute" accession="ERX942065">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942065</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#62</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815453, constructed from sample accession ERS625488 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625488" refname="GPS_MW_3027-sc-2139660" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625488</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_3027-sc-2139660</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815453</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#63" center_name="The Wellcome Trust Sanger Institute" accession="ERX942066">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942066</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#63</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#63</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815465, constructed from sample accession ERS625489 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625489" refname="GPS_MW_5576-sc-2139661" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625489</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_5576-sc-2139661</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815465</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#64" center_name="The Wellcome Trust Sanger Institute" accession="ERX942067">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942067</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#64</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#64</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815477, constructed from sample accession ERS625490 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625490" refname="GPS_MW_1641-sc-2139662" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625490</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1641-sc-2139662</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815477</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#65" center_name="The Wellcome Trust Sanger Institute" accession="ERX942068">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942068</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#65</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#65</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815394, constructed from sample accession ERS625493 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625493" refname="GPS_MW_1727-sc-2139665" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625493</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1727-sc-2139665</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815394</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#66" center_name="The Wellcome Trust Sanger Institute" accession="ERX942069">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942069</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#66</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#66</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815406, constructed from sample accession ERS625494 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625494" refname="GPS_MW_2020-sc-2139666" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625494</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2020-sc-2139666</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815406</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#67" center_name="The Wellcome Trust Sanger Institute" accession="ERX942070">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942070</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#67</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815418, constructed from sample accession ERS625495 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625495" refname="GPS_MW_2707-sc-2139667" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625495</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2707-sc-2139667</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815418</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#68" center_name="The Wellcome Trust Sanger Institute" accession="ERX942071">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942071</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#68</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815430, constructed from sample accession ERS625496 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625496" refname="GPS_MW_736-sc-2139668" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625496</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_736-sc-2139668</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815430</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#69" center_name="The Wellcome Trust Sanger Institute" accession="ERX942072">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942072</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#69</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#69</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815442, constructed from sample accession ERS625497 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625497" refname="GPS_MW_1145-sc-2139669" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625497</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1145-sc-2139669</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815442</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#70" center_name="The Wellcome Trust Sanger Institute" accession="ERX942073">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942073</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#70</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#70</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815454, constructed from sample accession ERS625498 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625498" refname="GPS_MW_5372-sc-2139670" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625498</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_5372-sc-2139670</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815454</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#72" center_name="The Wellcome Trust Sanger Institute" accession="ERX942075">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942075</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#72</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#72</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815478, constructed from sample accession ERS625500 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence GACGGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625500" refname="GPS_MW_2565-sc-2139672" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625500</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2565-sc-2139672</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815478</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#73" center_name="The Wellcome Trust Sanger Institute" accession="ERX942076">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942076</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#73</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#73</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815395, constructed from sample accession ERS625501 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625501" refname="GPS_MW_5702-sc-2139673" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625501</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_5702-sc-2139673</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815395</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#74" center_name="The Wellcome Trust Sanger Institute" accession="ERX942077">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942077</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#74</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815407, constructed from sample accession ERS625502 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625502" refname="GPS_MW_2494-sc-2139674" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625502</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2494-sc-2139674</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815407</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#75" center_name="The Wellcome Trust Sanger Institute" accession="ERX942078">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942078</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#75</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815419, constructed from sample accession ERS625503 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence GAATCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625503" refname="GPS_MW_3106-sc-2139675" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625503</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_3106-sc-2139675</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815419</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#76" center_name="The Wellcome Trust Sanger Institute" accession="ERX942079">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942079</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#76</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815431, constructed from sample accession ERS625504 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625504" refname="GPS_MW_2230-sc-2139676" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625504</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2230-sc-2139676</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815431</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#77" center_name="The Wellcome Trust Sanger Institute" accession="ERX942080">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942080</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#77</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815443, constructed from sample accession ERS625505 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625505" refname="GPS_MW_203-sc-2139677" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625505</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_203-sc-2139677</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815443</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#78" center_name="The Wellcome Trust Sanger Institute" accession="ERX942081">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942081</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#78</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#78</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815455, constructed from sample accession ERS625506 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625506" refname="GPS_MW_987-sc-2139678" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625506</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_987-sc-2139678</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815455</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#79" center_name="The Wellcome Trust Sanger Institute" accession="ERX942082">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942082</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#79</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815467, constructed from sample accession ERS625507 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625507" refname="GPS_MW_374-sc-2139679" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625507</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_374-sc-2139679</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815467</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#80" center_name="The Wellcome Trust Sanger Institute" accession="ERX942083">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942083</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#80</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815479, constructed from sample accession ERS625508 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence GTCGCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625508" refname="GPS_MW_2845-sc-2139680" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625508</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2845-sc-2139680</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815479</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#81" center_name="The Wellcome Trust Sanger Institute" accession="ERX942084">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942084</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#81</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815396, constructed from sample accession ERS625509 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625509" refname="GPS_MW_320-sc-2139681" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625509</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_320-sc-2139681</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815396</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#82" center_name="The Wellcome Trust Sanger Institute" accession="ERX942085">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942085</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#82</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#82</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815408, constructed from sample accession ERS625510 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625510" refname="GPS_MW_1413-sc-2139682" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625510</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1413-sc-2139682</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815408</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#83" center_name="The Wellcome Trust Sanger Institute" accession="ERX942086">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942086</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#83</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#83</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815420, constructed from sample accession ERS625511 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence GCTCCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625511" refname="GPS_MW_514-sc-2139683" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625511</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_514-sc-2139683</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815420</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#85" center_name="The Wellcome Trust Sanger Institute" accession="ERX942088">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942088</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#85</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#85</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815444, constructed from sample accession ERS625513 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence GAGGATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625513" refname="GPS_MW_239-sc-2139685" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625513</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_239-sc-2139685</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815444</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#86" center_name="The Wellcome Trust Sanger Institute" accession="ERX942089">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942089</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#86</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815456, constructed from sample accession ERS625514 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence GTTGTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625514" refname="GPS_MW_4159-sc-2139686" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625514</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_4159-sc-2139686</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815456</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#87" center_name="The Wellcome Trust Sanger Institute" accession="ERX942090">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942090</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#87</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815468, constructed from sample accession ERS625515 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence GGATTAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625515" refname="GPS_MW_1967-sc-2139687" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625515</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1967-sc-2139687</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815468</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#88" center_name="The Wellcome Trust Sanger Institute" accession="ERX942091">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942091</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#88</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#88</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815480, constructed from sample accession ERS625516 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence GATAGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625516" refname="GPS_MW_1683-sc-2139688" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625516</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1683-sc-2139688</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815480</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#89" center_name="The Wellcome Trust Sanger Institute" accession="ERX942092">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942092</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#89</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#89</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815397, constructed from sample accession ERS625517 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence GTGTGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625517" refname="GPS_MW_1260-sc-2139689" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625517</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1260-sc-2139689</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815397</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#90" center_name="The Wellcome Trust Sanger Institute" accession="ERX942093">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942093</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#90</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#90</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815409, constructed from sample accession ERS625518 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence GCAATCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625518" refname="GPS_MW_1324-sc-2139690" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625518</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1324-sc-2139690</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815409</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#91" center_name="The Wellcome Trust Sanger Institute" accession="ERX942094">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942094</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#91</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#91</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815421, constructed from sample accession ERS625519 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence GACCTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625519" refname="GPS_MW_2378-sc-2139691" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625519</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2378-sc-2139691</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815421</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#92" center_name="The Wellcome Trust Sanger Institute" accession="ERX942095">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942095</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#92</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#92</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815433, constructed from sample accession ERS625520 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence GCCTGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625520" refname="GPS_MW_1541-sc-2139692" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625520</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1541-sc-2139692</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815433</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#93" center_name="The Wellcome Trust Sanger Institute" accession="ERX942096">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942096</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#93</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#93</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815445, constructed from sample accession ERS625521 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence GCACTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625521" refname="GPS_MW_1019-sc-2139693" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625521</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1019-sc-2139693</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815445</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#94" center_name="The Wellcome Trust Sanger Institute" accession="ERX942097">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942097</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#94</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#94</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815457, constructed from sample accession ERS625522 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence GCTAACTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625522" refname="GPS_MW_4375-sc-2139694" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625522</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_4375-sc-2139694</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815457</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#95" center_name="The Wellcome Trust Sanger Institute" accession="ERX942098">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942098</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#95</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#95</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815469, constructed from sample accession ERS625523 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence GATTCATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625523" refname="GPS_MW_1615-sc-2139695" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625523</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1615-sc-2139695</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815469</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#1" center_name="The Wellcome Trust Sanger Institute" accession="ERX942099">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942099</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826865, constructed from sample accession ERS625524 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625524" refname="GPS_MW_663-sc-2139696" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625524</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_663-sc-2139696</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826865</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#2" center_name="The Wellcome Trust Sanger Institute" accession="ERX942100">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942100</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826877, constructed from sample accession ERS625525 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625525" refname="GPS_MW_883-sc-2139697" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625525</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_883-sc-2139697</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826877</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#3" center_name="The Wellcome Trust Sanger Institute" accession="ERX942101">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942101</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826889, constructed from sample accession ERS625526 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625526" refname="GPS_MW_2770-sc-2139698" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625526</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2770-sc-2139698</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826889</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#4" center_name="The Wellcome Trust Sanger Institute" accession="ERX942102">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942102</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826901, constructed from sample accession ERS625527 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625527" refname="GPS_MW_4702-sc-2139699" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625527</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_4702-sc-2139699</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826901</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#5" center_name="The Wellcome Trust Sanger Institute" accession="ERX942103">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942103</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826913, constructed from sample accession ERS625528 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625528" refname="GPS_MW_95-sc-2139700" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625528</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_95-sc-2139700</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826913</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#6" center_name="The Wellcome Trust Sanger Institute" accession="ERX942104">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942104</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826925, constructed from sample accession ERS625529 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625529" refname="GPS_MW_144-sc-2139701" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625529</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_144-sc-2139701</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826925</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#7" center_name="The Wellcome Trust Sanger Institute" accession="ERX942105">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942105</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826937, constructed from sample accession ERS625530 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625530" refname="GPS_MW_4966-sc-2139702" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625530</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_4966-sc-2139702</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826937</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX942106">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942106</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826949, constructed from sample accession ERS625531 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625531" refname="GPS_MW_606-sc-2139703" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625531</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_606-sc-2139703</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826949</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#9" center_name="The Wellcome Trust Sanger Institute" accession="ERX942107">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942107</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826866, constructed from sample accession ERS625532 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625532" refname="GPS_MW_5500-sc-2139704" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625532</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_5500-sc-2139704</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826866</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#10" center_name="The Wellcome Trust Sanger Institute" accession="ERX942108">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942108</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826878, constructed from sample accession ERS625533 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625533" refname="GPS_MW_4786-sc-2139705" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625533</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_4786-sc-2139705</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826878</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#11" center_name="The Wellcome Trust Sanger Institute" accession="ERX942109">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942109</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826890, constructed from sample accession ERS625534 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625534" refname="GPS_MW_456-sc-2139706" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625534</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_456-sc-2139706</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826890</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#12" center_name="The Wellcome Trust Sanger Institute" accession="ERX942110">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942110</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826902, constructed from sample accession ERS625535 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625535" refname="GPS_MW_5-sc-2139707" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625535</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_5-sc-2139707</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826902</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#13" center_name="The Wellcome Trust Sanger Institute" accession="ERX942111">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942111</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826914, constructed from sample accession ERS625536 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625536" refname="GPS_MW_1199-sc-2139708" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625536</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1199-sc-2139708</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826914</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#14" center_name="The Wellcome Trust Sanger Institute" accession="ERX942112">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942112</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826926, constructed from sample accession ERS625537 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625537" refname="GPS_MW_786-sc-2139709" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625537</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_786-sc-2139709</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826926</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#15" center_name="The Wellcome Trust Sanger Institute" accession="ERX942113">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942113</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826938, constructed from sample accession ERS625538 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625538" refname="GPS_MW_1883-sc-2139710" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625538</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1883-sc-2139710</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826938</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#16" center_name="The Wellcome Trust Sanger Institute" accession="ERX942114">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942114</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826950, constructed from sample accession ERS625539 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625539" refname="GPS_MW_2649-sc-2139711" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625539</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2649-sc-2139711</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826950</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#17" center_name="The Wellcome Trust Sanger Institute" accession="ERX942115">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942115</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826867, constructed from sample accession ERS625540 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625540" refname="GPS_MW_1796-sc-2139712" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625540</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1796-sc-2139712</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826867</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#1" center_name="The Wellcome Trust Sanger Institute" accession="ERX941909">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941909</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810434, constructed from sample accession ERS625387 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625387" refname="GPS_MW_A26988_R1-sc-2139558" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625387</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_A26988_R1-sc-2139558</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810434</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#2" center_name="The Wellcome Trust Sanger Institute" accession="ERX941910">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941910</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810446, constructed from sample accession ERS625388 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625388" refname="GPS_MW_D38253_R1-sc-2139559" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625388</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_D38253_R1-sc-2139559</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810446</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#3" center_name="The Wellcome Trust Sanger Institute" accession="ERX941911">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941911</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810458, constructed from sample accession ERS625390 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625390" refname="GPS_MW_1390-sc-2139561" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625390</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1390-sc-2139561</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810458</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#6" center_name="The Wellcome Trust Sanger Institute" accession="ERX941914">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941914</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810494, constructed from sample accession ERS625396 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625396" refname="GPS_MW_C17415_R1-sc-2139567" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625396</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_C17415_R1-sc-2139567</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810494</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX941916">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941916</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810518, constructed from sample accession ERS625398 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625398" refname="GPS_MW_C13233_R1-sc-2139569" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625398</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_C13233_R1-sc-2139569</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810518</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#9" center_name="The Wellcome Trust Sanger Institute" accession="ERX941917">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941917</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810435, constructed from sample accession ERS625406 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625406" refname="GPS_MW_D39268_R1-sc-2139577" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625406</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_D39268_R1-sc-2139577</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810435</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#10" center_name="The Wellcome Trust Sanger Institute" accession="ERX941918">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941918</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810447, constructed from sample accession ERS625422 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625422" refname="GPS_MW_1449-sc-2139593" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625422</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1449-sc-2139593</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810447</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#11" center_name="The Wellcome Trust Sanger Institute" accession="ERX941919">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941919</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810459, constructed from sample accession ERS625491 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625491" refname="GPS_MW_713-sc-2139663" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625491</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_713-sc-2139663</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810459</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#12" center_name="The Wellcome Trust Sanger Institute" accession="ERX941920">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941920</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810471, constructed from sample accession ERS625492 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625492" refname="GPS_MW_3229-sc-2139664" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625492</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_3229-sc-2139664</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810471</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#18" center_name="The Wellcome Trust Sanger Institute" accession="ERX942116">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942116</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826879, constructed from sample accession ERS625541 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625541" refname="GPS_MW_3622-sc-2139713" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625541</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_3622-sc-2139713</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826879</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#19" center_name="The Wellcome Trust Sanger Institute" accession="ERX942117">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942117</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826891, constructed from sample accession ERS625542 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625542" refname="GPS_MW_1368-sc-2139714" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625542</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1368-sc-2139714</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826891</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#20" center_name="The Wellcome Trust Sanger Institute" accession="ERX942118">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942118</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826903, constructed from sample accession ERS625543 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625543" refname="GPS_MW_958-sc-2139715" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625543</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_958-sc-2139715</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826903</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#21" center_name="The Wellcome Trust Sanger Institute" accession="ERX942119">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942119</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826915, constructed from sample accession ERS625544 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625544" refname="GPS_MW_1090-sc-2139716" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625544</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1090-sc-2139716</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826915</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#22" center_name="The Wellcome Trust Sanger Institute" accession="ERX942120">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942120</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826927, constructed from sample accession ERS625546 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625546" refname="GPS_MW_4854-sc-2139718" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625546</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_4854-sc-2139718</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826927</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#23" center_name="The Wellcome Trust Sanger Institute" accession="ERX942121">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942121</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826939, constructed from sample accession ERS625548 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625548" refname="GPS_MW_BIP1H9-sc-2139720" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625548</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_BIP1H9-sc-2139720</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826939</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#24" center_name="The Wellcome Trust Sanger Institute" accession="ERX942122">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942122</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826951, constructed from sample accession ERS625549 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625549" refname="GPS_MW_BIP1JU-sc-2139721" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625549</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_BIP1JU-sc-2139721</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826951</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#25" center_name="The Wellcome Trust Sanger Institute" accession="ERX942123">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942123</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826868, constructed from sample accession ERS625550 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625550" refname="GPS_MW_BIP1JS-sc-2139722" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625550</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_BIP1JS-sc-2139722</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826868</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#26" center_name="The Wellcome Trust Sanger Institute" accession="ERX942124">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942124</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826880, constructed from sample accession ERS625552 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625552" refname="GPS_MW_BIP1I1-sc-2139724" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625552</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_BIP1I1-sc-2139724</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826880</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#27" center_name="The Wellcome Trust Sanger Institute" accession="ERX942125">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942125</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826892, constructed from sample accession ERS625553 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625553" refname="GPS_MW_BKR2VM-sc-2139725" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625553</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_BKR2VM-sc-2139725</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826892</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#29" center_name="The Wellcome Trust Sanger Institute" accession="ERX942127">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942127</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826916, constructed from sample accession ERS625555 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625555" refname="GPS_MW_1024121-sc-2139727" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625555</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1024121-sc-2139727</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826916</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#30" center_name="The Wellcome Trust Sanger Institute" accession="ERX942128">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942128</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826928, constructed from sample accession ERS625556 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625556" refname="GPS_MW_1037340-sc-2139728" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625556</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1037340-sc-2139728</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826928</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#13" center_name="The Wellcome Trust Sanger Institute" accession="ERX941921">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941921</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810483, constructed from sample accession ERS625545 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625545" refname="GPS_MW_2949-sc-2139717" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625545</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2949-sc-2139717</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810483</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#14" center_name="The Wellcome Trust Sanger Institute" accession="ERX941922">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941922</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810495, constructed from sample accession ERS625547 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625547" refname="GPS_MW_BHA4DN-sc-2139719" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625547</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_BHA4DN-sc-2139719</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810495</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#15" center_name="The Wellcome Trust Sanger Institute" accession="ERX941923">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941923</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810507, constructed from sample accession ERS625551 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625551" refname="GPS_MW_BKQ6YX-sc-2139723" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625551</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_BKQ6YX-sc-2139723</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810507</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#17" center_name="The Wellcome Trust Sanger Institute" accession="ERX941925">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941925</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810436, constructed from sample accession ERS625645 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625645" refname="GPS_MW_155273-sc-2139818" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625645</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_155273-sc-2139818</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810436</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#18" center_name="The Wellcome Trust Sanger Institute" accession="ERX941926">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941926</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810448, constructed from sample accession ERS625651 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625651" refname="GPS_MW_2470-sc-2139824" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625651</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2470-sc-2139824</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810448</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#19" center_name="The Wellcome Trust Sanger Institute" accession="ERX941927">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941927</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810460, constructed from sample accession ERS625657 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625657" refname="GPS_MW_1863-sc-2139830" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625657</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1863-sc-2139830</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810460</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#20" center_name="The Wellcome Trust Sanger Institute" accession="ERX941928">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941928</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810472, constructed from sample accession ERS625667 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625667" refname="GPS_MW_18664-sc-2139840" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625667</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_18664-sc-2139840</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810472</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#21" center_name="The Wellcome Trust Sanger Institute" accession="ERX941929">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941929</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810484, constructed from sample accession ERS625718 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625718" refname="GPS_MW_1958-sc-2139892" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625718</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1958-sc-2139892</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810484</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#22" center_name="The Wellcome Trust Sanger Institute" accession="ERX941930">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941930</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810496, constructed from sample accession ERS625931 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625931" refname="GPS_MW_A60380-sc-2139933" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625931</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_A60380-sc-2139933</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810496</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#23" center_name="The Wellcome Trust Sanger Institute" accession="ERX941931">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941931</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810508, constructed from sample accession ERS626999 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS626999" refname="GPS_GM_0900-sc-2190313" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS626999</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_0900-sc-2190313</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810508</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#24" center_name="The Wellcome Trust Sanger Institute" accession="ERX941932">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941932</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810520, constructed from sample accession ERS627000 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627000" refname="GPS_GM_0901-sc-2190314" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627000</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_0901-sc-2190314</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810520</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX942130">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942130</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826952, constructed from sample accession ERS625558 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625558" refname="GPS_MW_BQN1D8-sc-2139730" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625558</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_BQN1D8-sc-2139730</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826952</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX942131">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942131</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826869, constructed from sample accession ERS625559 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625559" refname="GPS_MW_BQN1DL-sc-2139731" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625559</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_BQN1DL-sc-2139731</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826869</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX942132">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942132</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826881, constructed from sample accession ERS625561 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625561" refname="GPS_MW_BQN1E3-sc-2139733" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625561</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_BQN1E3-sc-2139733</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826881</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX942133">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942133</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826893, constructed from sample accession ERS625562 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625562" refname="GPS_MW_BQN1BP-sc-2139734" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625562</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_BQN1BP-sc-2139734</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826893</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX942134">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942134</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826905, constructed from sample accession ERS625563 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625563" refname="GPS_MW_BQN4MI-sc-2139735" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625563</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_BQN4MI-sc-2139735</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826905</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX942135">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942135</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826917, constructed from sample accession ERS625564 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625564" refname="GPS_MW_BQN1FT-sc-2139736" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625564</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_BQN1FT-sc-2139736</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826917</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX942136">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942136</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826929, constructed from sample accession ERS625565 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625565" refname="GPS_MW_BQN1ET-sc-2139737" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625565</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_BQN1ET-sc-2139737</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826929</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#39" center_name="The Wellcome Trust Sanger Institute" accession="ERX942137">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942137</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#39</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826941, constructed from sample accession ERS625566 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625566" refname="GPS_MW_BQN16G-sc-2139738" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625566</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_BQN16G-sc-2139738</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826941</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#40" center_name="The Wellcome Trust Sanger Institute" accession="ERX942138">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942138</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#40</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826953, constructed from sample accession ERS625567 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625567" refname="GPS_MW_18631-sc-2139739" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625567</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_18631-sc-2139739</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826953</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#41" center_name="The Wellcome Trust Sanger Institute" accession="ERX942139">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942139</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#41</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826870, constructed from sample accession ERS625568 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625568" refname="GPS_MW_18626-sc-2139740" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625568</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_18626-sc-2139740</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826870</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#42" center_name="The Wellcome Trust Sanger Institute" accession="ERX942140">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942140</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#42</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826882, constructed from sample accession ERS625569 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625569" refname="GPS_MW_BQN10M-sc-2139741" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625569</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_BQN10M-sc-2139741</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826882</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#43" center_name="The Wellcome Trust Sanger Institute" accession="ERX942141">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942141</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#43</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826894, constructed from sample accession ERS625570 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625570" refname="GPS_MW_BQN18P-sc-2139742" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625570</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_BQN18P-sc-2139742</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826894</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#26" center_name="The Wellcome Trust Sanger Institute" accession="ERX941934">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941934</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810449, constructed from sample accession ERS627006 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627006" refname="GPS_GM_0905-sc-2190320" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627006</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_0905-sc-2190320</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810449</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#27" center_name="The Wellcome Trust Sanger Institute" accession="ERX941935">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941935</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810461, constructed from sample accession ERS627007 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627007" refname="GPS_GM_0906-sc-2190321" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627007</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_0906-sc-2190321</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810461</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#28" center_name="The Wellcome Trust Sanger Institute" accession="ERX941936">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941936</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810473, constructed from sample accession ERS627008 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627008" refname="GPS_GM_0907-sc-2190322" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627008</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_0907-sc-2190322</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810473</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#29" center_name="The Wellcome Trust Sanger Institute" accession="ERX941937">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941937</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810485, constructed from sample accession ERS627011 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627011" refname="GPS_GM_0909-sc-2190325" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627011</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_0909-sc-2190325</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810485</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#30" center_name="The Wellcome Trust Sanger Institute" accession="ERX941938">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941938</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810497, constructed from sample accession ERS627017 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627017" refname="GPS_GM_0913-sc-2190331" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627017</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_0913-sc-2190331</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810497</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX941939">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941939</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810509, constructed from sample accession ERS627019 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627019" refname="GPS_GM_0914-sc-2190333" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627019</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_0914-sc-2190333</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810509</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX941940">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941940</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810521, constructed from sample accession ERS627025 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627025" refname="GPS_GM_0918-sc-2190339" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627025</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_0918-sc-2190339</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810521</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX941941">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941941</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810438, constructed from sample accession ERS627026 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627026" refname="GPS_GM_0919-sc-2190340" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627026</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_0919-sc-2190340</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810438</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX941942">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941942</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810450, constructed from sample accession ERS627027 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627027" refname="GPS_GM_0920-sc-2190341" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627027</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_0920-sc-2190341</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810450</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX941943">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941943</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810462, constructed from sample accession ERS627033 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627033" refname="GPS_GM_0923-sc-2190347" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627033</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_0923-sc-2190347</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810462</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX941944">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941944</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810474, constructed from sample accession ERS627034 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627034" refname="GPS_GM_0924-sc-2190348" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627034</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_0924-sc-2190348</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810474</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX941945">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941945</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810486, constructed from sample accession ERS627037 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627037" refname="GPS_GM_0926-sc-2190351" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627037</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_0926-sc-2190351</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810486</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX941946">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941946</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810498, constructed from sample accession ERS627038 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627038" refname="GPS_GM_0927-sc-2190352" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627038</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_0927-sc-2190352</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810498</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#44" center_name="The Wellcome Trust Sanger Institute" accession="ERX942142">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942142</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#44</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826906, constructed from sample accession ERS625571 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625571" refname="GPS_MW_18640-sc-2139743" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625571</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_18640-sc-2139743</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826906</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#45" center_name="The Wellcome Trust Sanger Institute" accession="ERX942143">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942143</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#45</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826918, constructed from sample accession ERS625572 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625572" refname="GPS_MW_18743-sc-2139744" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625572</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_18743-sc-2139744</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826918</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#46" center_name="The Wellcome Trust Sanger Institute" accession="ERX942144">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942144</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#46</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826930, constructed from sample accession ERS625573 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625573" refname="GPS_MW_D54465-sc-2139745" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625573</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_D54465-sc-2139745</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826930</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#47" center_name="The Wellcome Trust Sanger Institute" accession="ERX942145">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942145</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#47</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826942, constructed from sample accession ERS625574 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625574" refname="GPS_MW_18821-sc-2139746" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625574</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_18821-sc-2139746</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826942</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#48" center_name="The Wellcome Trust Sanger Institute" accession="ERX942146">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942146</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#48</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826954, constructed from sample accession ERS625575 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625575" refname="GPS_MW_19069-sc-2139748" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625575</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_19069-sc-2139748</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826954</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#49" center_name="The Wellcome Trust Sanger Institute" accession="ERX942147">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942147</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#49</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826871, constructed from sample accession ERS625576 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625576" refname="GPS_MW_1869-sc-2139749" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625576</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1869-sc-2139749</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826871</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#50" center_name="The Wellcome Trust Sanger Institute" accession="ERX942148">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942148</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#50</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826883, constructed from sample accession ERS625577 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625577" refname="GPS_MW_155009-sc-2139750" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625577</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_155009-sc-2139750</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826883</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#51" center_name="The Wellcome Trust Sanger Institute" accession="ERX942149">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942149</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#51</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826895, constructed from sample accession ERS625578 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625578" refname="GPS_MW_18655-sc-2139751" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625578</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_18655-sc-2139751</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826895</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#52" center_name="The Wellcome Trust Sanger Institute" accession="ERX942150">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942150</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#52</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826907, constructed from sample accession ERS625579 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625579" refname="GPS_MW_18922-sc-2139752" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625579</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_18922-sc-2139752</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826907</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#53" center_name="The Wellcome Trust Sanger Institute" accession="ERX942151">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942151</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#53</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826919, constructed from sample accession ERS625580 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625580" refname="GPS_MW_1783-sc-2139753" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625580</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1783-sc-2139753</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826919</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#54" center_name="The Wellcome Trust Sanger Institute" accession="ERX942152">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942152</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#54</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826931, constructed from sample accession ERS625581 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625581" refname="GPS_MW_4515-sc-2139754" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625581</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_4515-sc-2139754</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826931</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#55" center_name="The Wellcome Trust Sanger Institute" accession="ERX942153">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942153</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#55</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826943, constructed from sample accession ERS625582 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625582" refname="GPS_MW_154700-sc-2139755" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625582</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_154700-sc-2139755</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826943</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#56" center_name="The Wellcome Trust Sanger Institute" accession="ERX942154">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942154</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#56</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826955, constructed from sample accession ERS625583 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625583" refname="GPS_MW_155017-sc-2139756" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625583</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_155017-sc-2139756</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826955</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#39" center_name="The Wellcome Trust Sanger Institute" accession="ERX941947">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941947</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#39</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810510, constructed from sample accession ERS627040 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627040" refname="GPS_GM_0928-sc-2190354" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627040</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_0928-sc-2190354</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810510</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#40" center_name="The Wellcome Trust Sanger Institute" accession="ERX941948">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941948</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#40</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810522, constructed from sample accession ERS627043 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627043" refname="GPS_GM_0930-sc-2190357" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627043</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_0930-sc-2190357</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810522</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#41" center_name="The Wellcome Trust Sanger Institute" accession="ERX941949">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941949</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#41</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810439, constructed from sample accession ERS627053 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627053" refname="GPS_GM_0937-sc-2190367" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627053</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_0937-sc-2190367</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810439</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#42" center_name="The Wellcome Trust Sanger Institute" accession="ERX941950">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941950</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#42</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810451, constructed from sample accession ERS627063 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627063" refname="GPS_GM_0946-sc-2190377" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627063</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_0946-sc-2190377</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810451</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#43" center_name="The Wellcome Trust Sanger Institute" accession="ERX941951">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941951</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#43</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810463, constructed from sample accession ERS627066 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627066" refname="GPS_GM_0948-sc-2190380" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627066</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_0948-sc-2190380</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810463</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#44" center_name="The Wellcome Trust Sanger Institute" accession="ERX941952">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941952</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#44</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810475, constructed from sample accession ERS627068 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627068" refname="GPS_GM_0949-sc-2190382" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627068</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_0949-sc-2190382</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810475</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#45" center_name="The Wellcome Trust Sanger Institute" accession="ERX941953">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941953</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#45</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810487, constructed from sample accession ERS627071 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627071" refname="GPS_GM_0951-sc-2190385" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627071</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_0951-sc-2190385</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810487</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#46" center_name="The Wellcome Trust Sanger Institute" accession="ERX941954">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941954</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#46</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810499, constructed from sample accession ERS627079 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627079" refname="GPS_GM_0957-sc-2190393" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627079</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_0957-sc-2190393</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810499</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#47" center_name="The Wellcome Trust Sanger Institute" accession="ERX941955">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941955</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#47</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810511, constructed from sample accession ERS627093 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627093" refname="GPS_GM_0966-sc-2190407" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627093</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_0966-sc-2190407</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810511</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#48" center_name="The Wellcome Trust Sanger Institute" accession="ERX941956">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941956</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#48</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810523, constructed from sample accession ERS627097 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627097" refname="GPS_GM_0969-sc-2190411" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627097</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_0969-sc-2190411</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810523</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#49" center_name="The Wellcome Trust Sanger Institute" accession="ERX941957">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941957</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#49</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810440, constructed from sample accession ERS627104 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627104" refname="GPS_GM_0974-sc-2190418" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627104</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_0974-sc-2190418</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810440</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#50" center_name="The Wellcome Trust Sanger Institute" accession="ERX941958">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941958</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#50</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810452, constructed from sample accession ERS627109 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627109" refname="GPS_GM_0977-sc-2190423" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627109</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_0977-sc-2190423</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810452</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#51" center_name="The Wellcome Trust Sanger Institute" accession="ERX941959">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941959</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#51</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810464, constructed from sample accession ERS627039 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627039" refname="GPS_GM_1005-sc-2190353" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627039</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_1005-sc-2190353</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810464</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#57" center_name="The Wellcome Trust Sanger Institute" accession="ERX942155">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942155</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#57</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826872, constructed from sample accession ERS625584 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625584" refname="GPS_MW_18994-sc-2139757" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625584</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_18994-sc-2139757</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826872</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#58" center_name="The Wellcome Trust Sanger Institute" accession="ERX942156">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942156</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#58</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826884, constructed from sample accession ERS625585 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625585" refname="GPS_MW_18864-sc-2139758" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625585</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_18864-sc-2139758</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826884</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#59" center_name="The Wellcome Trust Sanger Institute" accession="ERX942157">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942157</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#59</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826896, constructed from sample accession ERS625586 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625586" refname="GPS_MW_19082-sc-2139759" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625586</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_19082-sc-2139759</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826896</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#60" center_name="The Wellcome Trust Sanger Institute" accession="ERX942158">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942158</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#60</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#60</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826908, constructed from sample accession ERS625587 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625587" refname="GPS_MW_1610-sc-2139760" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625587</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1610-sc-2139760</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826908</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#61" center_name="The Wellcome Trust Sanger Institute" accession="ERX942159">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942159</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#61</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826920, constructed from sample accession ERS625588 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625588" refname="GPS_MW_2909-sc-2139761" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625588</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2909-sc-2139761</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826920</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#62" center_name="The Wellcome Trust Sanger Institute" accession="ERX942160">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942160</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#62</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826932, constructed from sample accession ERS625589 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625589" refname="GPS_MW_5697-sc-2139762" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625589</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_5697-sc-2139762</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826932</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#63" center_name="The Wellcome Trust Sanger Institute" accession="ERX942161">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942161</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#63</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#63</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826944, constructed from sample accession ERS625590 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625590" refname="GPS_MW_154721-sc-2139763" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625590</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_154721-sc-2139763</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826944</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#64" center_name="The Wellcome Trust Sanger Institute" accession="ERX942162">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942162</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#64</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#64</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826956, constructed from sample accession ERS625591 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625591" refname="GPS_MW_18650-sc-2139764" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625591</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_18650-sc-2139764</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826956</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#65" center_name="The Wellcome Trust Sanger Institute" accession="ERX942163">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942163</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#65</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#65</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826873, constructed from sample accession ERS625592 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625592" refname="GPS_MW_18654-sc-2139765" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625592</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_18654-sc-2139765</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826873</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#66" center_name="The Wellcome Trust Sanger Institute" accession="ERX942164">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942164</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#66</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#66</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826885, constructed from sample accession ERS625593 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625593" refname="GPS_MW_2298-sc-2139766" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625593</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2298-sc-2139766</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826885</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#67" center_name="The Wellcome Trust Sanger Institute" accession="ERX942165">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942165</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#67</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826897, constructed from sample accession ERS625594 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625594" refname="GPS_MW_1715-sc-2139767" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625594</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1715-sc-2139767</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826897</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#68" center_name="The Wellcome Trust Sanger Institute" accession="ERX942166">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942166</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#68</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826909, constructed from sample accession ERS625595 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625595" refname="GPS_MW_5065-sc-2139768" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625595</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_5065-sc-2139768</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826909</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#69" center_name="The Wellcome Trust Sanger Institute" accession="ERX942167">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942167</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#69</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#69</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826921, constructed from sample accession ERS625596 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625596" refname="GPS_MW_938-sc-2139769" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625596</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_938-sc-2139769</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826921</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#52" center_name="The Wellcome Trust Sanger Institute" accession="ERX941960">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941960</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#52</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810476, constructed from sample accession ERS627144 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627144" refname="GPS_GM_1045-sc-2190459" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627144</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_1045-sc-2190459</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810476</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#53" center_name="The Wellcome Trust Sanger Institute" accession="ERX941961">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941961</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#53</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810488, constructed from sample accession ERS627175 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627175" refname="GPS_GM_1076-sc-2190490" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627175</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_1076-sc-2190490</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810488</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#54" center_name="The Wellcome Trust Sanger Institute" accession="ERX941962">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941962</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#54</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810500, constructed from sample accession ERS627179 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627179" refname="GPS_GM_1080-sc-2190494" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627179</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_1080-sc-2190494</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810500</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#55" center_name="The Wellcome Trust Sanger Institute" accession="ERX941963">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941963</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#55</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810512, constructed from sample accession ERS627183 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627183" refname="GPS_GM_1084-sc-2190498" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627183</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_1084-sc-2190498</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810512</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#56" center_name="The Wellcome Trust Sanger Institute" accession="ERX941964">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941964</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#56</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810524, constructed from sample accession ERS627190 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627190" refname="GPS_GM_1091-sc-2190506" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627190</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_1091-sc-2190506</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810524</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#57" center_name="The Wellcome Trust Sanger Institute" accession="ERX941965">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941965</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#57</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810441, constructed from sample accession ERS627191 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627191" refname="GPS_GM_1092-sc-2190507" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627191</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_1092-sc-2190507</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810441</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#58" center_name="The Wellcome Trust Sanger Institute" accession="ERX941966">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941966</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#58</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810453, constructed from sample accession ERS627192 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627192" refname="GPS_GM_1093-sc-2190508" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627192</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_1093-sc-2190508</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810453</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#59" center_name="The Wellcome Trust Sanger Institute" accession="ERX941967">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941967</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#59</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810465, constructed from sample accession ERS627193 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627193" refname="GPS_GM_1094-sc-2190509" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627193</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_1094-sc-2190509</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810465</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#60" center_name="The Wellcome Trust Sanger Institute" accession="ERX941968">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941968</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#60</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#60</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810477, constructed from sample accession ERS627194 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627194" refname="GPS_GM_1095-sc-2190510" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627194</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_1095-sc-2190510</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810477</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#61" center_name="The Wellcome Trust Sanger Institute" accession="ERX941969">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941969</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#61</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810489, constructed from sample accession ERS627195 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627195" refname="GPS_GM_1096-sc-2190511" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627195</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_1096-sc-2190511</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810489</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#62" center_name="The Wellcome Trust Sanger Institute" accession="ERX941970">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941970</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#62</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810501, constructed from sample accession ERS627196 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627196" refname="GPS_GM_1097-sc-2190512" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627196</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_1097-sc-2190512</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810501</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#63" center_name="The Wellcome Trust Sanger Institute" accession="ERX941971">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941971</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#63</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#63</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810513, constructed from sample accession ERS627206 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS627206" refname="GPS_GM_1107-sc-2190522" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS627206</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_GM_1107-sc-2190522</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810513</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#64" center_name="The Wellcome Trust Sanger Institute" accession="ERX941972">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941972</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#64</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#64</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810525, constructed from sample accession ERS625385 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625385" refname="GPS_MW_C13355_R1-sc-2139556" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625385</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_C13355_R1-sc-2139556</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810525</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#70" center_name="The Wellcome Trust Sanger Institute" accession="ERX942168">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942168</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#70</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#70</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826933, constructed from sample accession ERS625597 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625597" refname="GPS_MW_498-sc-2139770" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625597</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_498-sc-2139770</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826933</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#71" center_name="The Wellcome Trust Sanger Institute" accession="ERX942169">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942169</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#71</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#71</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826945, constructed from sample accession ERS625598 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence GTGTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625598" refname="GPS_MW_155271-sc-2139771" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625598</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_155271-sc-2139771</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826945</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#72" center_name="The Wellcome Trust Sanger Institute" accession="ERX942170">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942170</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#72</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#72</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826957, constructed from sample accession ERS625599 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence GACGGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625599" refname="GPS_MW_18847-sc-2139772" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625599</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_18847-sc-2139772</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826957</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#73" center_name="The Wellcome Trust Sanger Institute" accession="ERX942171">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942171</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#73</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#73</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826874, constructed from sample accession ERS625600 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625600" refname="GPS_MW_18788-sc-2139773" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625600</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_18788-sc-2139773</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826874</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#74" center_name="The Wellcome Trust Sanger Institute" accession="ERX942172">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942172</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#74</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826886, constructed from sample accession ERS625601 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625601" refname="GPS_MW_1750-sc-2139774" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625601</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1750-sc-2139774</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826886</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#75" center_name="The Wellcome Trust Sanger Institute" accession="ERX942173">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942173</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#75</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826898, constructed from sample accession ERS625602 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence GAATCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625602" refname="GPS_MW_A59818-sc-2139775" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625602</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_A59818-sc-2139775</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826898</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#76" center_name="The Wellcome Trust Sanger Institute" accession="ERX942174">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942174</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#76</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826910, constructed from sample accession ERS625603 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625603" refname="GPS_MW_19111-sc-2139776" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625603</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_19111-sc-2139776</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826910</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#77" center_name="The Wellcome Trust Sanger Institute" accession="ERX942175">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942175</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#77</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826922, constructed from sample accession ERS625604 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625604" refname="GPS_MW_2358-sc-2139777" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625604</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2358-sc-2139777</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826922</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#78" center_name="The Wellcome Trust Sanger Institute" accession="ERX942176">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942176</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#78</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#78</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826934, constructed from sample accession ERS625605 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625605" refname="GPS_MW_1858-sc-2139778" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625605</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1858-sc-2139778</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826934</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#79" center_name="The Wellcome Trust Sanger Institute" accession="ERX942177">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942177</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#79</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826946, constructed from sample accession ERS625606 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625606" refname="GPS_MW_155016-sc-2139779" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625606</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_155016-sc-2139779</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826946</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#80" center_name="The Wellcome Trust Sanger Institute" accession="ERX942178">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942178</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#80</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826958, constructed from sample accession ERS625607 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence GTCGCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625607" refname="GPS_MW_C23520-sc-2139780" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625607</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_C23520-sc-2139780</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826958</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#81" center_name="The Wellcome Trust Sanger Institute" accession="ERX942179">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942179</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#81</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826875, constructed from sample accession ERS625608 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625608" refname="GPS_MW_18956-sc-2139781" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625608</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_18956-sc-2139781</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826875</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#82" center_name="The Wellcome Trust Sanger Institute" accession="ERX942180">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942180</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#82</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#82</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826887, constructed from sample accession ERS625609 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625609" refname="GPS_MW_2053-sc-2139782" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625609</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2053-sc-2139782</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826887</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#65" center_name="The Wellcome Trust Sanger Institute" accession="ERX941973">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941973</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#65</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#65</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810442, constructed from sample accession ERS625386 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625386" refname="GPS_MW_C14798_R1-sc-2139557" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625386</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_C14798_R1-sc-2139557</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810442</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#66" center_name="The Wellcome Trust Sanger Institute" accession="ERX941974">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941974</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#66</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#66</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810454, constructed from sample accession ERS625389 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625389" refname="GPS_MW_C14650_R1-sc-2139560" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625389</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_C14650_R1-sc-2139560</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810454</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#67" center_name="The Wellcome Trust Sanger Institute" accession="ERX941975">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941975</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#67</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810466, constructed from sample accession ERS625392 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625392" refname="GPS_MW_2168-sc-2139563" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625392</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2168-sc-2139563</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810466</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#68" center_name="The Wellcome Trust Sanger Institute" accession="ERX941976">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941976</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#68</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810478, constructed from sample accession ERS625393 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625393" refname="GPS_MW_927-sc-2139564" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625393</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_927-sc-2139564</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810478</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#69" center_name="The Wellcome Trust Sanger Institute" accession="ERX941977">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941977</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#69</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#69</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810490, constructed from sample accession ERS625394 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625394" refname="GPS_MW_5048-sc-2139565" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625394</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_5048-sc-2139565</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810490</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#70" center_name="The Wellcome Trust Sanger Institute" accession="ERX941978">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941978</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#70</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#70</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810502, constructed from sample accession ERS625399 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625399" refname="GPS_MW_2438-sc-2139570" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625399</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2438-sc-2139570</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810502</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#71" center_name="The Wellcome Trust Sanger Institute" accession="ERX941979">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941979</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#71</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#71</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810514, constructed from sample accession ERS625400 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence GTGTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625400" refname="GPS_MW_2485-sc-2139571" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625400</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2485-sc-2139571</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810514</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#72" center_name="The Wellcome Trust Sanger Institute" accession="ERX941980">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941980</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#72</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#72</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810526, constructed from sample accession ERS625401 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence GACGGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625401" refname="GPS_MW_2444-sc-2139572" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625401</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2444-sc-2139572</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810526</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#73" center_name="The Wellcome Trust Sanger Institute" accession="ERX941981">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941981</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#73</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#73</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810443, constructed from sample accession ERS625402 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625402" refname="GPS_MW_2762-sc-2139573" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625402</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2762-sc-2139573</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810443</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#74" center_name="The Wellcome Trust Sanger Institute" accession="ERX941982">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941982</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#74</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810455, constructed from sample accession ERS625403 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625403" refname="GPS_MW_D7940_R1-sc-2139574" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625403</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_D7940_R1-sc-2139574</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810455</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#76" center_name="The Wellcome Trust Sanger Institute" accession="ERX941984">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941984</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#76</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810479, constructed from sample accession ERS625405 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625405" refname="GPS_MW_2279-sc-2139576" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625405</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2279-sc-2139576</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810479</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#77" center_name="The Wellcome Trust Sanger Institute" accession="ERX941985">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941985</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#77</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810491, constructed from sample accession ERS625407 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625407" refname="GPS_MW_D49723_R1-sc-2139578" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625407</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_D49723_R1-sc-2139578</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810491</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#83" center_name="The Wellcome Trust Sanger Institute" accession="ERX942181">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942181</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#83</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#83</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826899, constructed from sample accession ERS625610 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence GCTCCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625610" refname="GPS_MW_1974-sc-2139783" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625610</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1974-sc-2139783</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826899</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#84" center_name="The Wellcome Trust Sanger Institute" accession="ERX942182">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942182</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#84</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#84</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826911, constructed from sample accession ERS625611 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence GTAAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625611" refname="GPS_MW_2439-sc-2139784" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625611</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2439-sc-2139784</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826911</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#85" center_name="The Wellcome Trust Sanger Institute" accession="ERX942183">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942183</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#85</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#85</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826923, constructed from sample accession ERS625612 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence GAGGATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625612" refname="GPS_MW_2414-sc-2139785" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625612</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2414-sc-2139785</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826923</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#86" center_name="The Wellcome Trust Sanger Institute" accession="ERX942184">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942184</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#86</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826935, constructed from sample accession ERS625613 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence GTTGTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625613" refname="GPS_MW_1788-sc-2139786" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625613</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1788-sc-2139786</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826935</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#87" center_name="The Wellcome Trust Sanger Institute" accession="ERX942185">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942185</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#87</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826947, constructed from sample accession ERS625614 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence GGATTAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625614" refname="GPS_MW_154692-sc-2139787" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625614</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_154692-sc-2139787</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826947</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#88" center_name="The Wellcome Trust Sanger Institute" accession="ERX942186">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942186</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#88</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#88</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826959, constructed from sample accession ERS625615 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence GATAGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625615" refname="GPS_MW_19071-sc-2139788" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625615</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_19071-sc-2139788</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826959</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#89" center_name="The Wellcome Trust Sanger Institute" accession="ERX942187">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942187</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#89</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#89</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826876, constructed from sample accession ERS625616 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence GTGTGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625616" refname="GPS_MW_18863-sc-2139789" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625616</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_18863-sc-2139789</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826876</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#90" center_name="The Wellcome Trust Sanger Institute" accession="ERX942188">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942188</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#90</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#90</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826888, constructed from sample accession ERS625617 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence GCAATCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625617" refname="GPS_MW_7107-sc-2139790" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625617</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_7107-sc-2139790</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826888</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#91" center_name="The Wellcome Trust Sanger Institute" accession="ERX942189">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942189</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#91</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#91</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826900, constructed from sample accession ERS625618 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence GACCTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625618" refname="GPS_MW_19198-sc-2139791" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625618</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_19198-sc-2139791</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826900</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#92" center_name="The Wellcome Trust Sanger Institute" accession="ERX942190">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942190</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#92</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#92</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826912, constructed from sample accession ERS625619 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence GCCTGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625619" refname="GPS_MW_770-sc-2139792" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625619</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_770-sc-2139792</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826912</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#93" center_name="The Wellcome Trust Sanger Institute" accession="ERX942191">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942191</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#93</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#93</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826924, constructed from sample accession ERS625620 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence GCACTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625620" refname="GPS_MW_19120-sc-2139793" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625620</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_19120-sc-2139793</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826924</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#94" center_name="The Wellcome Trust Sanger Institute" accession="ERX942192">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942192</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#94</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#94</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826936, constructed from sample accession ERS625621 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence GCTAACTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625621" refname="GPS_MW_C23697-sc-2139794" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625621</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_C23697-sc-2139794</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826936</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_4#95" center_name="The Wellcome Trust Sanger Institute" accession="ERX942193">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942193</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_4#95</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_4#95</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12826948, constructed from sample accession ERS625622 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_4).  This submission includes reads tagged with the sequence GATTCATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625622" refname="GPS_MW_154984-sc-2139795" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625622</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_154984-sc-2139795</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12826948</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#78" center_name="The Wellcome Trust Sanger Institute" accession="ERX941986">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941986</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#78</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#78</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810503, constructed from sample accession ERS625408 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625408" refname="GPS_MW_D7887_R1-sc-2139579" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625408</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_D7887_R1-sc-2139579</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810503</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#79" center_name="The Wellcome Trust Sanger Institute" accession="ERX941987">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941987</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#79</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810515, constructed from sample accession ERS625409 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625409" refname="GPS_MW_2254-sc-2139580" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625409</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2254-sc-2139580</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810515</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#80" center_name="The Wellcome Trust Sanger Institute" accession="ERX941988">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941988</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#80</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810527, constructed from sample accession ERS625410 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence GTCGCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625410" refname="GPS_MW_2923-sc-2139581" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625410</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2923-sc-2139581</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810527</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#81" center_name="The Wellcome Trust Sanger Institute" accession="ERX941989">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941989</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#81</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810444, constructed from sample accession ERS625411 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625411" refname="GPS_MW_4827-sc-2139582" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625411</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_4827-sc-2139582</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810444</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#82" center_name="The Wellcome Trust Sanger Institute" accession="ERX941990">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941990</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#82</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#82</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810456, constructed from sample accession ERS625412 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625412" refname="GPS_MW_4944-sc-2139583" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625412</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_4944-sc-2139583</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810456</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#83" center_name="The Wellcome Trust Sanger Institute" accession="ERX941991">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941991</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#83</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#83</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810468, constructed from sample accession ERS625413 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence GCTCCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625413" refname="GPS_MW_C15275_R1-sc-2139584" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625413</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_C15275_R1-sc-2139584</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810468</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#84" center_name="The Wellcome Trust Sanger Institute" accession="ERX941992">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941992</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#84</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#84</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810480, constructed from sample accession ERS625414 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence GTAAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625414" refname="GPS_MW_C16950_R1-sc-2139585" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625414</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_C16950_R1-sc-2139585</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810480</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#85" center_name="The Wellcome Trust Sanger Institute" accession="ERX941993">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941993</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#85</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#85</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810492, constructed from sample accession ERS625415 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence GAGGATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625415" refname="GPS_MW_C17600_R1-sc-2139586" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625415</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_C17600_R1-sc-2139586</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810492</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#86" center_name="The Wellcome Trust Sanger Institute" accession="ERX941994">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941994</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#86</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810504, constructed from sample accession ERS625416 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence GTTGTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625416" refname="GPS_MW_C17622_R1-sc-2139587" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625416</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_C17622_R1-sc-2139587</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810504</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#87" center_name="The Wellcome Trust Sanger Institute" accession="ERX941995">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941995</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#87</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810516, constructed from sample accession ERS625417 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence GGATTAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625417" refname="GPS_MW_C7186_R1-sc-2139588" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625417</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_C7186_R1-sc-2139588</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810516</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#88" center_name="The Wellcome Trust Sanger Institute" accession="ERX941996">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941996</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#88</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#88</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810528, constructed from sample accession ERS625418 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence GATAGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625418" refname="GPS_MW_C9864_R1-sc-2139589" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625418</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_C9864_R1-sc-2139589</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810528</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#89" center_name="The Wellcome Trust Sanger Institute" accession="ERX941997">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941997</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#89</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#89</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810445, constructed from sample accession ERS625419 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence GTGTGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625419" refname="GPS_MW_D11449_R1-sc-2139590" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625419</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_D11449_R1-sc-2139590</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810445</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#90" center_name="The Wellcome Trust Sanger Institute" accession="ERX941998">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941998</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#90</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#90</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810457, constructed from sample accession ERS625420 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence GCAATCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625420" refname="GPS_MW_D40036_R1-sc-2139591" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625420</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_D40036_R1-sc-2139591</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810457</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#92" center_name="The Wellcome Trust Sanger Institute" accession="ERX942000">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942000</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#92</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#92</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810481, constructed from sample accession ERS625423 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence GCCTGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625423" refname="GPS_MW_2684-sc-2139594" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625423</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2684-sc-2139594</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810481</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#93" center_name="The Wellcome Trust Sanger Institute" accession="ERX942001">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942001</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#93</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#93</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810493, constructed from sample accession ERS625424 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence GCACTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625424" refname="GPS_MW_5859-sc-2139595" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625424</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_5859-sc-2139595</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810493</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#94" center_name="The Wellcome Trust Sanger Institute" accession="ERX942002">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942002</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#94</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#94</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810505, constructed from sample accession ERS625425 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence GCTAACTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625425" refname="GPS_MW_1396-sc-2139596" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625425</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1396-sc-2139596</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810505</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_2#95" center_name="The Wellcome Trust Sanger Institute" accession="ERX942003">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942003</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_2#95</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_2#95</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12810517, constructed from sample accession ERS625426 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_2).  This submission includes reads tagged with the sequence GATTCATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625426" refname="GPS_MW_5689-sc-2139597" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625426</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_5689-sc-2139597</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12810517</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#1" center_name="The Wellcome Trust Sanger Institute" accession="ERX942004">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942004</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815386, constructed from sample accession ERS625427 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625427" refname="GPS_MW_953-sc-2139598" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625427</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_953-sc-2139598</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815386</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#2" center_name="The Wellcome Trust Sanger Institute" accession="ERX942005">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942005</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815398, constructed from sample accession ERS625428 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625428" refname="GPS_MW_912-sc-2139599" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625428</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_912-sc-2139599</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815398</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#3" center_name="The Wellcome Trust Sanger Institute" accession="ERX942006">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942006</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815410, constructed from sample accession ERS625429 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625429" refname="GPS_MW_1580-sc-2139600" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625429</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1580-sc-2139600</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815410</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#4" center_name="The Wellcome Trust Sanger Institute" accession="ERX942007">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942007</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815422, constructed from sample accession ERS625430 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625430" refname="GPS_MW_1137-sc-2139601" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625430</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1137-sc-2139601</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815422</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#5" center_name="The Wellcome Trust Sanger Institute" accession="ERX942008">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942008</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815434, constructed from sample accession ERS625431 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625431" refname="GPS_MW_2652-sc-2139602" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625431</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2652-sc-2139602</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815434</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#6" center_name="The Wellcome Trust Sanger Institute" accession="ERX942009">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942009</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815446, constructed from sample accession ERS625432 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625432" refname="GPS_MW_140-sc-2139603" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625432</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_140-sc-2139603</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815446</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#7" center_name="The Wellcome Trust Sanger Institute" accession="ERX942010">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942010</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815458, constructed from sample accession ERS625433 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625433" refname="GPS_MW_1784-sc-2139604" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625433</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1784-sc-2139604</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815458</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX942011">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942011</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815470, constructed from sample accession ERS625434 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625434" refname="GPS_MW_3602-sc-2139605" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625434</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_3602-sc-2139605</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815470</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#9" center_name="The Wellcome Trust Sanger Institute" accession="ERX942012">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942012</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815387, constructed from sample accession ERS625435 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625435" refname="GPS_MW_3856-sc-2139606" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625435</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_3856-sc-2139606</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815387</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#10" center_name="The Wellcome Trust Sanger Institute" accession="ERX942013">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942013</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815399, constructed from sample accession ERS625436 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625436" refname="GPS_MW_3407-sc-2139607" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625436</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_3407-sc-2139607</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815399</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#11" center_name="The Wellcome Trust Sanger Institute" accession="ERX942014">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942014</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815411, constructed from sample accession ERS625437 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625437" refname="GPS_MW_3451-sc-2139608" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625437</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_3451-sc-2139608</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815411</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#12" center_name="The Wellcome Trust Sanger Institute" accession="ERX942015">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942015</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815423, constructed from sample accession ERS625438 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625438" refname="GPS_MW_595-sc-2139609" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625438</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_595-sc-2139609</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815423</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#13" center_name="The Wellcome Trust Sanger Institute" accession="ERX942016">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942016</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815435, constructed from sample accession ERS625439 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625439" refname="GPS_MW_2364-sc-2139610" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625439</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2364-sc-2139610</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815435</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#14" center_name="The Wellcome Trust Sanger Institute" accession="ERX942017">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942017</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815447, constructed from sample accession ERS625440 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625440" refname="GPS_MW_2318-sc-2139611" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625440</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2318-sc-2139611</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815447</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#15" center_name="The Wellcome Trust Sanger Institute" accession="ERX942018">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942018</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815459, constructed from sample accession ERS625441 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625441" refname="GPS_MW_1627-sc-2139612" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625441</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1627-sc-2139612</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815459</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#16" center_name="The Wellcome Trust Sanger Institute" accession="ERX942019">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942019</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815471, constructed from sample accession ERS625442 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625442" refname="GPS_MW_1905-sc-2139613" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625442</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1905-sc-2139613</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815471</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#17" center_name="The Wellcome Trust Sanger Institute" accession="ERX942020">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942020</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815388, constructed from sample accession ERS625443 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625443" refname="GPS_MW_3359-sc-2139614" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625443</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_3359-sc-2139614</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815388</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#18" center_name="The Wellcome Trust Sanger Institute" accession="ERX942021">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942021</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815400, constructed from sample accession ERS625444 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625444" refname="GPS_MW_1006-sc-2139615" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625444</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1006-sc-2139615</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815400</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#19" center_name="The Wellcome Trust Sanger Institute" accession="ERX942022">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942022</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815412, constructed from sample accession ERS625445 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625445" refname="GPS_MW_1169-sc-2139616" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625445</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1169-sc-2139616</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815412</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#20" center_name="The Wellcome Trust Sanger Institute" accession="ERX942023">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942023</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815424, constructed from sample accession ERS625446 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625446" refname="GPS_MW_5469-sc-2139617" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625446</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_5469-sc-2139617</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815424</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#21" center_name="The Wellcome Trust Sanger Institute" accession="ERX942024">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942024</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815436, constructed from sample accession ERS625447 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625447" refname="GPS_MW_2940-sc-2139618" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625447</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2940-sc-2139618</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815436</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#22" center_name="The Wellcome Trust Sanger Institute" accession="ERX942025">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942025</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815448, constructed from sample accession ERS625448 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625448" refname="GPS_MW_1339-sc-2139619" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625448</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1339-sc-2139619</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815448</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#23" center_name="The Wellcome Trust Sanger Institute" accession="ERX942026">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942026</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815460, constructed from sample accession ERS625449 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625449" refname="GPS_MW_1467-sc-2139620" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625449</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1467-sc-2139620</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815460</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#24" center_name="The Wellcome Trust Sanger Institute" accession="ERX942027">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942027</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815472, constructed from sample accession ERS625450 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625450" refname="GPS_MW_1360-sc-2139621" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625450</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1360-sc-2139621</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815472</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#25" center_name="The Wellcome Trust Sanger Institute" accession="ERX942028">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942028</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815389, constructed from sample accession ERS625451 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625451" refname="GPS_MW_1832-sc-2139622" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625451</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1832-sc-2139622</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815389</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#26" center_name="The Wellcome Trust Sanger Institute" accession="ERX942029">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942029</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815401, constructed from sample accession ERS625452 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625452" refname="GPS_MW_2409-sc-2139623" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625452</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2409-sc-2139623</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815401</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#27" center_name="The Wellcome Trust Sanger Institute" accession="ERX942030">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942030</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815413, constructed from sample accession ERS625453 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625453" refname="GPS_MW_3169-sc-2139624" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625453</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_3169-sc-2139624</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815413</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#28" center_name="The Wellcome Trust Sanger Institute" accession="ERX942031">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942031</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815425, constructed from sample accession ERS625454 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625454" refname="GPS_MW_4130-sc-2139625" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625454</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_4130-sc-2139625</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815425</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#29" center_name="The Wellcome Trust Sanger Institute" accession="ERX942032">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942032</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815437, constructed from sample accession ERS625455 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625455" refname="GPS_MW_3466-sc-2139626" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625455</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_3466-sc-2139626</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815437</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#30" center_name="The Wellcome Trust Sanger Institute" accession="ERX942033">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942033</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815449, constructed from sample accession ERS625456 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625456" refname="GPS_MW_1732-sc-2139627" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625456</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1732-sc-2139627</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815449</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX942034">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942034</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815461, constructed from sample accession ERS625457 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625457" refname="GPS_MW_3248-sc-2139628" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625457</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_3248-sc-2139628</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815461</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX942035">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942035</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815473, constructed from sample accession ERS625458 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625458" refname="GPS_MW_1867-sc-2139629" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625458</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1867-sc-2139629</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815473</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX942036">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942036</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815390, constructed from sample accession ERS625459 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625459" refname="GPS_MW_6217-sc-2139630" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625459</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_6217-sc-2139630</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815390</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX942037">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942037</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815402, constructed from sample accession ERS625460 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625460" refname="GPS_MW_6240-sc-2139631" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625460</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_6240-sc-2139631</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815402</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX942038">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942038</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815414, constructed from sample accession ERS625461 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625461" refname="GPS_MW_1865-sc-2139632" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625461</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1865-sc-2139632</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815414</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX942039">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942039</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815426, constructed from sample accession ERS625462 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625462" refname="GPS_MW_1558-sc-2139633" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625462</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1558-sc-2139633</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815426</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX942040">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942040</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815438, constructed from sample accession ERS625463 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625463" refname="GPS_MW_1030-sc-2139634" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625463</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1030-sc-2139634</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815438</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX942041">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942041</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815450, constructed from sample accession ERS625464 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625464" refname="GPS_MW_846-sc-2139635" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625464</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_846-sc-2139635</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815450</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#39" center_name="The Wellcome Trust Sanger Institute" accession="ERX942042">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942042</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#39</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815462, constructed from sample accession ERS625465 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625465" refname="GPS_MW_1938-sc-2139636" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625465</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1938-sc-2139636</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815462</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#40" center_name="The Wellcome Trust Sanger Institute" accession="ERX942043">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942043</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#40</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815474, constructed from sample accession ERS625466 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625466" refname="GPS_MW_2022-sc-2139637" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625466</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2022-sc-2139637</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815474</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#41" center_name="The Wellcome Trust Sanger Institute" accession="ERX942044">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942044</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#41</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815391, constructed from sample accession ERS625467 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625467" refname="GPS_MW_3350-sc-2139638" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625467</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_3350-sc-2139638</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815391</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#42" center_name="The Wellcome Trust Sanger Institute" accession="ERX942045">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942045</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#42</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815403, constructed from sample accession ERS625468 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625468" refname="GPS_MW_1625-sc-2139639" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625468</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1625-sc-2139639</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815403</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#43" center_name="The Wellcome Trust Sanger Institute" accession="ERX942046">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942046</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#43</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815415, constructed from sample accession ERS625469 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625469" refname="GPS_MW_2660-sc-2139640" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625469</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2660-sc-2139640</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815415</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#44" center_name="The Wellcome Trust Sanger Institute" accession="ERX942047">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942047</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#44</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815427, constructed from sample accession ERS625470 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625470" refname="GPS_MW_1172-sc-2139641" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625470</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1172-sc-2139641</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815427</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#45" center_name="The Wellcome Trust Sanger Institute" accession="ERX942048">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942048</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#45</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815439, constructed from sample accession ERS625471 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625471" refname="GPS_MW_2870-sc-2139642" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625471</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_2870-sc-2139642</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815439</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#46" center_name="The Wellcome Trust Sanger Institute" accession="ERX942049">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942049</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#46</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815451, constructed from sample accession ERS625472 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625472" refname="GPS_MW_1349-sc-2139643" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625472</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_1349-sc-2139643</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815451</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15378_3#47" center_name="The Wellcome Trust Sanger Institute" accession="ERX942050">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX942050</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15378_3#47</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15378_3#47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP001505" refname="Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP001505</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Global_Pneumococcal_Sequencing__GPS__study_I-sc-2012-06-14T11:10:13Z-2245</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12815463, constructed from sample accession ERS625473 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15378_3).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS625473" refname="GPS_MW_466-sc-2139644" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS625473</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_MW_466-sc-2139644</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12815463</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
