<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="SC_EXP_15682_2#3" center_name="The Wellcome Trust Sanger Institute" accession="ERX963799">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963799</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029625, constructed from sample accession ERS629066 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629066" refname="GPS_PL_9332_11-sc-2191177" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629066</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_9332_11-sc-2191177</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029625</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#4" center_name="The Wellcome Trust Sanger Institute" accession="ERX963800">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963800</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_2#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 13029637, constructed from sample accession ERS629067 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629067" refname="GPS_PL_9447_11-sc-2191178" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629067</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_9447_11-sc-2191178</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029637</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#5" center_name="The Wellcome Trust Sanger Institute" accession="ERX963801">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963801</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_2#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 13029649, constructed from sample accession ERS629068 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629068" refname="GPS_PL_9541_11-sc-2191179" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629068</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_9541_11-sc-2191179</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029649</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#6" center_name="The Wellcome Trust Sanger Institute" accession="ERX963802">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963802</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029661, constructed from sample accession ERS629069 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629069" refname="GPS_PL_9840_11-sc-2191180" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629069</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_9840_11-sc-2191180</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029661</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#7" center_name="The Wellcome Trust Sanger Institute" accession="ERX963803">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963803</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_2#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 13029673, constructed from sample accession ERS629070 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629070" refname="GPS_PL_9862_11-sc-2191181" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629070</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_9862_11-sc-2191181</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029673</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX963804">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963804</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029685, constructed from sample accession ERS629071 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629071" refname="GPS_PL_9896_11-sc-2191182" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629071</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_9896_11-sc-2191182</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029685</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#9" center_name="The Wellcome Trust Sanger Institute" accession="ERX963805">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963805</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029602, constructed from sample accession ERS629072 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629072" refname="GPS_PL_10636_11-sc-2191183" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629072</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_10636_11-sc-2191183</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029602</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#10" center_name="The Wellcome Trust Sanger Institute" accession="ERX963806">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963806</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029614, constructed from sample accession ERS629073 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629073" refname="GPS_PL_10826_11-sc-2191184" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629073</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_10826_11-sc-2191184</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029614</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#11" center_name="The Wellcome Trust Sanger Institute" accession="ERX963807">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963807</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029626, constructed from sample accession ERS629074 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629074" refname="GPS_PL_10965_11-sc-2191185" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629074</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_10965_11-sc-2191185</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029626</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#12" center_name="The Wellcome Trust Sanger Institute" accession="ERX963808">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963808</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029638, constructed from sample accession ERS629075 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629075" refname="GPS_PL_10990_11-sc-2191186" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629075</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_10990_11-sc-2191186</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029638</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#13" center_name="The Wellcome Trust Sanger Institute" accession="ERX963809">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963809</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029650, constructed from sample accession ERS629076 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629076" refname="GPS_PL_145_12-sc-2191187" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629076</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_145_12-sc-2191187</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029650</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#14" center_name="The Wellcome Trust Sanger Institute" accession="ERX963810">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963810</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029662, constructed from sample accession ERS629077 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629077" refname="GPS_PL_193_12-sc-2191188" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629077</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_193_12-sc-2191188</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029662</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#15" center_name="The Wellcome Trust Sanger Institute" accession="ERX963811">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963811</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029674, constructed from sample accession ERS629078 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629078" refname="GPS_PL_258_12-sc-2191189" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629078</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_258_12-sc-2191189</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029674</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#41" center_name="The Wellcome Trust Sanger Institute" accession="ERX964007">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964007</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#41</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032750, constructed from sample accession ERS634700 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634700" refname="GPS_TH_BK_0565-sc-2191404" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634700</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0565-sc-2191404</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032750</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#42" center_name="The Wellcome Trust Sanger Institute" accession="ERX964008">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964008</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#42</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032762, constructed from sample accession ERS634701 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634701" refname="GPS_TH_BK_0568-sc-2191405" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634701</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0568-sc-2191405</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032762</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#43" center_name="The Wellcome Trust Sanger Institute" accession="ERX964009">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964009</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#43</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032774, constructed from sample accession ERS634702 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634702" refname="GPS_TH_BK_0569-sc-2191406" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634702</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0569-sc-2191406</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032774</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#44" center_name="The Wellcome Trust Sanger Institute" accession="ERX964010">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964010</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#44</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032787, constructed from sample accession ERS634703 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634703" refname="GPS_TH_BK_0572-sc-2191407" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634703</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0572-sc-2191407</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032787</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#45" center_name="The Wellcome Trust Sanger Institute" accession="ERX964011">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964011</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#45</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032809, constructed from sample accession ERS634704 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634704" refname="GPS_TH_BK_0578-sc-2191408" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634704</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0578-sc-2191408</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032809</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#46" center_name="The Wellcome Trust Sanger Institute" accession="ERX964012">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964012</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#46</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032831, constructed from sample accession ERS634705 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634705" refname="GPS_TH_BK_0581-sc-2191409" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634705</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0581-sc-2191409</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032831</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#47" center_name="The Wellcome Trust Sanger Institute" accession="ERX964013">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964013</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#47</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032853, constructed from sample accession ERS634706 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634706" refname="GPS_TH_BK_0586-sc-2191410" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634706</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0586-sc-2191410</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032853</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#48" center_name="The Wellcome Trust Sanger Institute" accession="ERX964014">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964014</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#48</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032882, constructed from sample accession ERS634707 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634707" refname="GPS_TH_BK_0587-sc-2191411" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634707</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0587-sc-2191411</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032882</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#49" center_name="The Wellcome Trust Sanger Institute" accession="ERX964015">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964015</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#49</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032751, constructed from sample accession ERS634708 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634708" refname="GPS_TH_BK_0588-sc-2191412" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634708</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0588-sc-2191412</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032751</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#50" center_name="The Wellcome Trust Sanger Institute" accession="ERX964016">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964016</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#50</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032763, constructed from sample accession ERS634709 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634709" refname="GPS_TH_BK_0590-sc-2191413" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634709</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0590-sc-2191413</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032763</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#51" center_name="The Wellcome Trust Sanger Institute" accession="ERX964017">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964017</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#51</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032775, constructed from sample accession ERS634710 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634710" refname="GPS_TH_BK_0591-sc-2191414" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634710</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0591-sc-2191414</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032775</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#52" center_name="The Wellcome Trust Sanger Institute" accession="ERX964018">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964018</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#52</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032788, constructed from sample accession ERS634711 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634711" refname="GPS_TH_BK_0593-sc-2191415" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634711</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0593-sc-2191415</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032788</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#53" center_name="The Wellcome Trust Sanger Institute" accession="ERX964019">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964019</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#53</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032811, constructed from sample accession ERS634712 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634712" refname="GPS_TH_BK_0594-sc-2191416" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634712</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0594-sc-2191416</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032811</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#16" center_name="The Wellcome Trust Sanger Institute" accession="ERX963812">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963812</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_2#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 13029686, constructed from sample accession ERS629079 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629079" refname="GPS_PL_440_12-sc-2191190" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629079</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_440_12-sc-2191190</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029686</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#17" center_name="The Wellcome Trust Sanger Institute" accession="ERX963813">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963813</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029603, constructed from sample accession ERS629080 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629080" refname="GPS_PL_503_12-sc-2191191" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629080</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_503_12-sc-2191191</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029603</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#18" center_name="The Wellcome Trust Sanger Institute" accession="ERX963814">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963814</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029615, constructed from sample accession ERS629081 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629081" refname="GPS_PL_587_12-sc-2191192" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629081</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_587_12-sc-2191192</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029615</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#19" center_name="The Wellcome Trust Sanger Institute" accession="ERX963815">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963815</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029627, constructed from sample accession ERS629082 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629082" refname="GPS_PL_2766_12-sc-2191193" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629082</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_2766_12-sc-2191193</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029627</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#20" center_name="The Wellcome Trust Sanger Institute" accession="ERX963816">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963816</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029639, constructed from sample accession ERS629083 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629083" refname="GPS_PL_3151_12-sc-2191194" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629083</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_3151_12-sc-2191194</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029639</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#21" center_name="The Wellcome Trust Sanger Institute" accession="ERX963817">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963817</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029651, constructed from sample accession ERS629084 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629084" refname="GPS_PL_3424_12-sc-2191195" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629084</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_3424_12-sc-2191195</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029651</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#22" center_name="The Wellcome Trust Sanger Institute" accession="ERX963818">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963818</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029663, constructed from sample accession ERS629085 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629085" refname="GPS_PL_3546_12-sc-2191196" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629085</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_3546_12-sc-2191196</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029663</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#23" center_name="The Wellcome Trust Sanger Institute" accession="ERX963819">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963819</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029675, constructed from sample accession ERS629086 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629086" refname="GPS_PL_4060_12-sc-2191197" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629086</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_4060_12-sc-2191197</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029675</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#24" center_name="The Wellcome Trust Sanger Institute" accession="ERX963820">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963820</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029687, constructed from sample accession ERS629087 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629087" refname="GPS_PL_4094_12-sc-2191198" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629087</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_4094_12-sc-2191198</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029687</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#25" center_name="The Wellcome Trust Sanger Institute" accession="ERX963821">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963821</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_2#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 13029604, constructed from sample accession ERS629088 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629088" refname="GPS_PL_4340_12-sc-2191199" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629088</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_4340_12-sc-2191199</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029604</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#26" center_name="The Wellcome Trust Sanger Institute" accession="ERX963822">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963822</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029616, constructed from sample accession ERS629089 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629089" refname="GPS_PL_4430_12-sc-2191200" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629089</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_4430_12-sc-2191200</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029616</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#27" center_name="The Wellcome Trust Sanger Institute" accession="ERX963823">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963823</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029628, constructed from sample accession ERS629090 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629090" refname="GPS_PL_4628_12-sc-2191201" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629090</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_4628_12-sc-2191201</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029628</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#28" center_name="The Wellcome Trust Sanger Institute" accession="ERX963824">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963824</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029640, constructed from sample accession ERS629091 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629091" refname="GPS_PL_5096_12-sc-2191202" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629091</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_5096_12-sc-2191202</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029640</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#54" center_name="The Wellcome Trust Sanger Institute" accession="ERX964020">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964020</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#54</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032832, constructed from sample accession ERS634713 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634713" refname="GPS_TH_BK_0595-sc-2191417" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634713</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0595-sc-2191417</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032832</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#55" center_name="The Wellcome Trust Sanger Institute" accession="ERX964021">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964021</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#55</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032854, constructed from sample accession ERS634714 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634714" refname="GPS_TH_BK_0597-sc-2191418" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634714</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0597-sc-2191418</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032854</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#56" center_name="The Wellcome Trust Sanger Institute" accession="ERX964022">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964022</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#56</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032884, constructed from sample accession ERS634715 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634715" refname="GPS_TH_BK_0598-sc-2191419" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634715</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0598-sc-2191419</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032884</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#57" center_name="The Wellcome Trust Sanger Institute" accession="ERX964023">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964023</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#57</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032752, constructed from sample accession ERS634716 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634716" refname="GPS_TH_BK_0601-sc-2191421" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634716</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0601-sc-2191421</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032752</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#58" center_name="The Wellcome Trust Sanger Institute" accession="ERX964024">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964024</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#58</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032764, constructed from sample accession ERS634717 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634717" refname="GPS_TH_BK_0603-sc-2191422" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634717</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0603-sc-2191422</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032764</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#59" center_name="The Wellcome Trust Sanger Institute" accession="ERX964025">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964025</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#59</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032776, constructed from sample accession ERS634718 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634718" refname="GPS_TH_BK_0604-sc-2191423" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634718</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0604-sc-2191423</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032776</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#60" center_name="The Wellcome Trust Sanger Institute" accession="ERX964026">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964026</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#60</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032789, constructed from sample accession ERS634719 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634719" refname="GPS_TH_BK_0605-sc-2191424" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634719</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0605-sc-2191424</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032789</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#61" center_name="The Wellcome Trust Sanger Institute" accession="ERX964027">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964027</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#61</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032813, constructed from sample accession ERS634720 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634720" refname="GPS_TH_BK_0606-sc-2191425" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634720</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0606-sc-2191425</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032813</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#62" center_name="The Wellcome Trust Sanger Institute" accession="ERX964028">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964028</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#62</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032834, constructed from sample accession ERS634721 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634721" refname="GPS_TH_BK_0611-sc-2191426" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634721</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0611-sc-2191426</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032834</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#63" center_name="The Wellcome Trust Sanger Institute" accession="ERX964029">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964029</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#63</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032856, constructed from sample accession ERS634722 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634722" refname="GPS_TH_BK_0613-sc-2191427" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634722</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0613-sc-2191427</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032856</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#64" center_name="The Wellcome Trust Sanger Institute" accession="ERX964030">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964030</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#64</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032886, constructed from sample accession ERS634723 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634723" refname="GPS_TH_BK_0619-sc-2191428" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634723</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0619-sc-2191428</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032886</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#65" center_name="The Wellcome Trust Sanger Institute" accession="ERX964031">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964031</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#65</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032753, constructed from sample accession ERS634724 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634724" refname="GPS_TH_BK_0620-sc-2191429" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634724</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0620-sc-2191429</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032753</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#66" center_name="The Wellcome Trust Sanger Institute" accession="ERX964032">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964032</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#66</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032765, constructed from sample accession ERS634725 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634725" refname="GPS_TH_BK_0626-sc-2191430" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634725</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0626-sc-2191430</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032765</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#29" center_name="The Wellcome Trust Sanger Institute" accession="ERX963825">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963825</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029652, constructed from sample accession ERS629092 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629092" refname="GPS_PL_5167_12-sc-2191203" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629092</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_5167_12-sc-2191203</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029652</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#30" center_name="The Wellcome Trust Sanger Institute" accession="ERX963826">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963826</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029664, constructed from sample accession ERS629093 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629093" refname="GPS_PL_5736_12-sc-2191204" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629093</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_5736_12-sc-2191204</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029664</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX963827">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963827</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029676, constructed from sample accession ERS629094 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629094" refname="GPS_PL_5955_12-sc-2191205" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629094</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_5955_12-sc-2191205</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029676</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX963828">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963828</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029688, constructed from sample accession ERS629095 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629095" refname="GPS_PL_6027_12-sc-2191206" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629095</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_6027_12-sc-2191206</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029688</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX963829">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963829</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029605, constructed from sample accession ERS629096 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629096" refname="GPS_PL_6051_12-sc-2191207" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629096</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_6051_12-sc-2191207</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029605</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX963830">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963830</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029617, constructed from sample accession ERS629097 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629097" refname="GPS_PL_6084_12-sc-2191208" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629097</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_6084_12-sc-2191208</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029617</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX963831">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963831</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029629, constructed from sample accession ERS629098 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629098" refname="GPS_PL_6090_12-sc-2191209" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629098</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_6090_12-sc-2191209</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029629</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX963832">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963832</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029641, constructed from sample accession ERS629099 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629099" refname="GPS_PL_6120_12-sc-2191210" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629099</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_6120_12-sc-2191210</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029641</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX963833">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963833</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029653, constructed from sample accession ERS629100 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629100" refname="GPS_PL_6157_12-sc-2191211" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629100</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_6157_12-sc-2191211</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029653</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX963834">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963834</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029665, constructed from sample accession ERS629101 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629101" refname="GPS_PL_6199_12-sc-2191212" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629101</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_6199_12-sc-2191212</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029665</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#39" center_name="The Wellcome Trust Sanger Institute" accession="ERX963835">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963835</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#39</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029677, constructed from sample accession ERS629102 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629102" refname="GPS_PL_6275_12-sc-2191213" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629102</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_6275_12-sc-2191213</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029677</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#40" center_name="The Wellcome Trust Sanger Institute" accession="ERX963836">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963836</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#40</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029689, constructed from sample accession ERS629103 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629103" refname="GPS_PL_6281_12-sc-2191214" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629103</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_6281_12-sc-2191214</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029689</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#41" center_name="The Wellcome Trust Sanger Institute" accession="ERX963837">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963837</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#41</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029606, constructed from sample accession ERS629104 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629104" refname="GPS_PL_6335_12-sc-2191215" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629104</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_6335_12-sc-2191215</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029606</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#67" center_name="The Wellcome Trust Sanger Institute" accession="ERX964033">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964033</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#67</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032777, constructed from sample accession ERS634726 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634726" refname="GPS_TH_BK_0630-sc-2191431" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634726</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0630-sc-2191431</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032777</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#68" center_name="The Wellcome Trust Sanger Institute" accession="ERX964034">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964034</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#68</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032790, constructed from sample accession ERS634727 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634727" refname="GPS_TH_BK_0631-sc-2191432" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634727</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0631-sc-2191432</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032790</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#69" center_name="The Wellcome Trust Sanger Institute" accession="ERX964035">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964035</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#69</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032814, constructed from sample accession ERS634728 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634728" refname="GPS_TH_BK_0633-sc-2191433" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634728</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0633-sc-2191433</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032814</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#70" center_name="The Wellcome Trust Sanger Institute" accession="ERX964036">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964036</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#70</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032836, constructed from sample accession ERS634729 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634729" refname="GPS_TH_BK_0635-sc-2191434" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634729</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0635-sc-2191434</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032836</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#71" center_name="The Wellcome Trust Sanger Institute" accession="ERX964037">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964037</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#71</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032858, constructed from sample accession ERS634730 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence GTGTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634730" refname="GPS_TH_BK_0636-sc-2191435" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634730</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0636-sc-2191435</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032858</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#72" center_name="The Wellcome Trust Sanger Institute" accession="ERX964038">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964038</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#72</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032889, constructed from sample accession ERS634731 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence GACGGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634731" refname="GPS_TH_BK_0637-sc-2191436" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634731</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0637-sc-2191436</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032889</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#73" center_name="The Wellcome Trust Sanger Institute" accession="ERX964039">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964039</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#73</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032754, constructed from sample accession ERS634732 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634732" refname="GPS_TH_BK_0638-sc-2191437" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634732</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0638-sc-2191437</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032754</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#74" center_name="The Wellcome Trust Sanger Institute" accession="ERX964040">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964040</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#74</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032766, constructed from sample accession ERS634733 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634733" refname="GPS_TH_BK_0639-sc-2191438" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634733</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0639-sc-2191438</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032766</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#75" center_name="The Wellcome Trust Sanger Institute" accession="ERX964041">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964041</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#75</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032778, constructed from sample accession ERS634734 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence GAATCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634734" refname="GPS_TH_BK_0640-sc-2191439" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634734</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0640-sc-2191439</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032778</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#76" center_name="The Wellcome Trust Sanger Institute" accession="ERX964042">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964042</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#76</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032791, constructed from sample accession ERS634735 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634735" refname="GPS_TH_BK_0641-sc-2191440" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634735</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0641-sc-2191440</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032791</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#78" center_name="The Wellcome Trust Sanger Institute" accession="ERX964044">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964044</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#78</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032839, constructed from sample accession ERS634737 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634737" refname="GPS_TH_BK_0648-sc-2191443" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634737</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0648-sc-2191443</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032839</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#79" center_name="The Wellcome Trust Sanger Institute" accession="ERX964045">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964045</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#79</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032860, constructed from sample accession ERS634738 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634738" refname="GPS_TH_BK_0651-sc-2191444" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634738</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0651-sc-2191444</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032860</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#42" center_name="The Wellcome Trust Sanger Institute" accession="ERX963838">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963838</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#42</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029618, constructed from sample accession ERS629105 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629105" refname="GPS_PL_6594_12-sc-2191216" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629105</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_6594_12-sc-2191216</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029618</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#43" center_name="The Wellcome Trust Sanger Institute" accession="ERX963839">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963839</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#43</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029630, constructed from sample accession ERS629106 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629106" refname="GPS_PL_6617_12-sc-2191217" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629106</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_6617_12-sc-2191217</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029630</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#44" center_name="The Wellcome Trust Sanger Institute" accession="ERX963840">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963840</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#44</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029642, constructed from sample accession ERS629107 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629107" refname="GPS_PL_6831_12-sc-2191218" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629107</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_6831_12-sc-2191218</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029642</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#45" center_name="The Wellcome Trust Sanger Institute" accession="ERX963841">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963841</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#45</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029654, constructed from sample accession ERS629108 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629108" refname="GPS_PL_7017_12-sc-2191219" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629108</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_7017_12-sc-2191219</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029654</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#46" center_name="The Wellcome Trust Sanger Institute" accession="ERX963842">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963842</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#46</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029666, constructed from sample accession ERS629109 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629109" refname="GPS_PL_7038_12-sc-2191220" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629109</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_7038_12-sc-2191220</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029666</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#47" center_name="The Wellcome Trust Sanger Institute" accession="ERX963843">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963843</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#47</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029678, constructed from sample accession ERS629110 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629110" refname="GPS_PL_7527_12-sc-2191221" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629110</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_7527_12-sc-2191221</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029678</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#48" center_name="The Wellcome Trust Sanger Institute" accession="ERX963844">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963844</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#48</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029690, constructed from sample accession ERS629111 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629111" refname="GPS_PL_7714_12-sc-2191222" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629111</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_7714_12-sc-2191222</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029690</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#49" center_name="The Wellcome Trust Sanger Institute" accession="ERX963845">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963845</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#49</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029607, constructed from sample accession ERS629112 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629112" refname="GPS_PL_115_13-sc-2191223" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629112</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_115_13-sc-2191223</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029607</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#50" center_name="The Wellcome Trust Sanger Institute" accession="ERX963846">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963846</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#50</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029619, constructed from sample accession ERS629113 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629113" refname="GPS_PL_449_13-sc-2191224" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629113</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_449_13-sc-2191224</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029619</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#51" center_name="The Wellcome Trust Sanger Institute" accession="ERX963847">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963847</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#51</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029631, constructed from sample accession ERS629114 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629114" refname="GPS_PL_611_13-sc-2191225" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629114</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_611_13-sc-2191225</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029631</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#52" center_name="The Wellcome Trust Sanger Institute" accession="ERX963848">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963848</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#52</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029643, constructed from sample accession ERS629115 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629115" refname="GPS_PL_830_13-sc-2191226" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629115</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_830_13-sc-2191226</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029643</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#53" center_name="The Wellcome Trust Sanger Institute" accession="ERX963849">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963849</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#53</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029655, constructed from sample accession ERS629116 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629116" refname="GPS_PL_1278_13-sc-2191227" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629116</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_1278_13-sc-2191227</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029655</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#54" center_name="The Wellcome Trust Sanger Institute" accession="ERX963850">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963850</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#54</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029667, constructed from sample accession ERS629117 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629117" refname="GPS_PL_1502_13-sc-2191228" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629117</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_1502_13-sc-2191228</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029667</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#80" center_name="The Wellcome Trust Sanger Institute" accession="ERX964046">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964046</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#80</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032891, constructed from sample accession ERS634739 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence GTCGCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634739" refname="GPS_TH_BK_0654-sc-2191445" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634739</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0654-sc-2191445</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032891</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#81" center_name="The Wellcome Trust Sanger Institute" accession="ERX964047">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964047</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#81</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032755, constructed from sample accession ERS634740 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634740" refname="GPS_TH_BK_0655-sc-2191446" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634740</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0655-sc-2191446</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032755</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#82" center_name="The Wellcome Trust Sanger Institute" accession="ERX964048">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964048</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#82</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032767, constructed from sample accession ERS634741 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634741" refname="GPS_TH_BK_0656-sc-2191447" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634741</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0656-sc-2191447</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032767</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#83" center_name="The Wellcome Trust Sanger Institute" accession="ERX964049">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964049</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#83</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032779, constructed from sample accession ERS634742 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence GCTCCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634742" refname="GPS_TH_BK_0657-sc-2191448" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634742</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0657-sc-2191448</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032779</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#84" center_name="The Wellcome Trust Sanger Institute" accession="ERX964050">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964050</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#84</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032794, constructed from sample accession ERS634743 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence GTAAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634743" refname="GPS_TH_BK_0658-sc-2191449" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634743</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0658-sc-2191449</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032794</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#85" center_name="The Wellcome Trust Sanger Institute" accession="ERX964051">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964051</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#85</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032818, constructed from sample accession ERS634744 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence GAGGATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634744" refname="GPS_TH_BK_0660-sc-2191450" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634744</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0660-sc-2191450</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032818</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#86" center_name="The Wellcome Trust Sanger Institute" accession="ERX964052">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964052</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#86</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032840, constructed from sample accession ERS634745 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence GTTGTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634745" refname="GPS_TH_BK_0661-sc-2191451" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634745</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0661-sc-2191451</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032840</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#87" center_name="The Wellcome Trust Sanger Institute" accession="ERX964053">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964053</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#87</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032862, constructed from sample accession ERS634746 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence GGATTAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634746" refname="GPS_TH_BK_0662-sc-2191452" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634746</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0662-sc-2191452</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032862</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#88" center_name="The Wellcome Trust Sanger Institute" accession="ERX964054">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964054</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#88</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032893, constructed from sample accession ERS634748 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence GATAGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634748" refname="GPS_TH_BK_0663-sc-2191454" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634748</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0663-sc-2191454</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032893</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#89" center_name="The Wellcome Trust Sanger Institute" accession="ERX964055">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964055</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#89</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032756, constructed from sample accession ERS634751 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence GTGTGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634751" refname="GPS_TH_BK_0667-sc-2191457" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634751</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0667-sc-2191457</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032756</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#90" center_name="The Wellcome Trust Sanger Institute" accession="ERX964056">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964056</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#90</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032768, constructed from sample accession ERS634754 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence GCAATCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634754" refname="GPS_TH_BK_0668-sc-2191460" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634754</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0668-sc-2191460</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032768</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#91" center_name="The Wellcome Trust Sanger Institute" accession="ERX964057">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964057</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#91</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032780, constructed from sample accession ERS634757 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence GACCTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634757" refname="GPS_TH_BK_0669-sc-2191463" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634757</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0669-sc-2191463</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032780</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#1" center_name="The Wellcome Trust Sanger Institute" accession="ERX964058">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964058</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041551, constructed from sample accession ERS634761 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634761" refname="GPS_TH_BK_0670-sc-2191467" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634761</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0670-sc-2191467</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041551</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#55" center_name="The Wellcome Trust Sanger Institute" accession="ERX963851">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963851</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#55</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029679, constructed from sample accession ERS629118 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629118" refname="GPS_PL_1695_13-sc-2191229" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629118</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_1695_13-sc-2191229</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029679</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#56" center_name="The Wellcome Trust Sanger Institute" accession="ERX963852">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963852</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#56</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029691, constructed from sample accession ERS629119 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629119" refname="GPS_PL_1718_13-sc-2191230" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629119</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_1718_13-sc-2191230</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029691</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#57" center_name="The Wellcome Trust Sanger Institute" accession="ERX963853">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963853</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#57</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029608, constructed from sample accession ERS629120 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629120" refname="GPS_PL_1921_13-sc-2191231" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629120</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_1921_13-sc-2191231</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029608</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#58" center_name="The Wellcome Trust Sanger Institute" accession="ERX963854">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963854</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#58</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029620, constructed from sample accession ERS629121 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629121" refname="GPS_PL_2231_13-sc-2191232" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629121</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_2231_13-sc-2191232</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029620</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#59" center_name="The Wellcome Trust Sanger Institute" accession="ERX963855">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963855</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#59</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029632, constructed from sample accession ERS629122 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629122" refname="GPS_PL_2370_13-sc-2191233" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629122</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_2370_13-sc-2191233</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029632</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#60" center_name="The Wellcome Trust Sanger Institute" accession="ERX963856">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963856</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#60</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029644, constructed from sample accession ERS629123 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629123" refname="GPS_PL_2693_13-sc-2191234" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629123</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_2693_13-sc-2191234</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029644</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#61" center_name="The Wellcome Trust Sanger Institute" accession="ERX963857">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963857</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#61</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029656, constructed from sample accession ERS629124 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629124" refname="GPS_PL_2820_13-sc-2191235" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629124</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_2820_13-sc-2191235</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029656</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#62" center_name="The Wellcome Trust Sanger Institute" accession="ERX963858">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963858</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#62</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029668, constructed from sample accession ERS629125 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629125" refname="GPS_PL_2825_13-sc-2191236" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629125</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_2825_13-sc-2191236</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029668</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#63" center_name="The Wellcome Trust Sanger Institute" accession="ERX963859">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963859</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#63</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029680, constructed from sample accession ERS629126 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629126" refname="GPS_PL_3095_13-sc-2191237" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629126</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_3095_13-sc-2191237</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029680</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#64" center_name="The Wellcome Trust Sanger Institute" accession="ERX963860">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963860</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#64</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029692, constructed from sample accession ERS629127 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629127" refname="GPS_PL_3257_13-sc-2191238" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629127</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_3257_13-sc-2191238</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029692</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#65" center_name="The Wellcome Trust Sanger Institute" accession="ERX963861">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963861</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#65</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029609, constructed from sample accession ERS629128 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629128" refname="GPS_PL_4205_13-sc-2191239" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629128</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_4205_13-sc-2191239</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029609</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#66" center_name="The Wellcome Trust Sanger Institute" accession="ERX963862">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963862</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#66</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029621, constructed from sample accession ERS629129 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629129" refname="GPS_PL_4367_13-sc-2191240" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629129</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_4367_13-sc-2191240</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029621</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#67" center_name="The Wellcome Trust Sanger Institute" accession="ERX963863">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963863</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#67</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029633, constructed from sample accession ERS629130 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629130" refname="GPS_PL_4382_13-sc-2191241" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629130</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_4382_13-sc-2191241</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029633</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#2" center_name="The Wellcome Trust Sanger Institute" accession="ERX964059">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964059</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041563, constructed from sample accession ERS634764 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634764" refname="GPS_TH_BK_0672-sc-2191470" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634764</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0672-sc-2191470</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041563</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#3" center_name="The Wellcome Trust Sanger Institute" accession="ERX964060">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964060</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041575, constructed from sample accession ERS634768 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634768" refname="GPS_TH_BK_0673-sc-2191474" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634768</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0673-sc-2191474</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041575</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#4" center_name="The Wellcome Trust Sanger Institute" accession="ERX964061">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964061</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041587, constructed from sample accession ERS634771 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634771" refname="GPS_TH_BK_0674-sc-2191477" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634771</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0674-sc-2191477</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041587</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#5" center_name="The Wellcome Trust Sanger Institute" accession="ERX964062">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964062</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041599, constructed from sample accession ERS634778 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634778" refname="GPS_TH_BK_0675-sc-2191484" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634778</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0675-sc-2191484</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041599</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#6" center_name="The Wellcome Trust Sanger Institute" accession="ERX964063">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964063</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041611, constructed from sample accession ERS634747 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634747" refname="GPS_TH_BK_0676-sc-2191453" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634747</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0676-sc-2191453</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041611</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#7" center_name="The Wellcome Trust Sanger Institute" accession="ERX964064">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964064</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041623, constructed from sample accession ERS634749 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634749" refname="GPS_TH_BK_0677-sc-2191455" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634749</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0677-sc-2191455</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041623</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX964065">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964065</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041635, constructed from sample accession ERS634750 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634750" refname="GPS_TH_BK_0679-sc-2191456" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634750</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0679-sc-2191456</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041635</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#9" center_name="The Wellcome Trust Sanger Institute" accession="ERX964066">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964066</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041552, constructed from sample accession ERS634752 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634752" refname="GPS_TH_BK_0680-sc-2191458" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634752</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0680-sc-2191458</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041552</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#10" center_name="The Wellcome Trust Sanger Institute" accession="ERX964067">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964067</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041564, constructed from sample accession ERS634753 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634753" refname="GPS_TH_BK_0682-sc-2191459" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634753</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0682-sc-2191459</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041564</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#11" center_name="The Wellcome Trust Sanger Institute" accession="ERX964068">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964068</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041576, constructed from sample accession ERS634755 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634755" refname="GPS_TH_BK_0684-sc-2191461" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634755</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0684-sc-2191461</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041576</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#12" center_name="The Wellcome Trust Sanger Institute" accession="ERX964069">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964069</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041588, constructed from sample accession ERS634756 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634756" refname="GPS_TH_BK_0686-sc-2191462" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634756</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0686-sc-2191462</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041588</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#13" center_name="The Wellcome Trust Sanger Institute" accession="ERX964070">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964070</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041600, constructed from sample accession ERS634758 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634758" refname="GPS_TH_BK_0689-sc-2191464" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634758</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0689-sc-2191464</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041600</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#14" center_name="The Wellcome Trust Sanger Institute" accession="ERX964071">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964071</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041612, constructed from sample accession ERS634759 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634759" refname="GPS_TH_BK_0692-sc-2191465" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634759</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0692-sc-2191465</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041612</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#68" center_name="The Wellcome Trust Sanger Institute" accession="ERX963864">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963864</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#68</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029645, constructed from sample accession ERS629131 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629131" refname="GPS_PL_4384_13-sc-2191242" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629131</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_4384_13-sc-2191242</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029645</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#69" center_name="The Wellcome Trust Sanger Institute" accession="ERX963865">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963865</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#69</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029657, constructed from sample accession ERS629132 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629132" refname="GPS_PL_4661_13-sc-2191243" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629132</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_4661_13-sc-2191243</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029657</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#70" center_name="The Wellcome Trust Sanger Institute" accession="ERX963866">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963866</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#70</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029669, constructed from sample accession ERS629133 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629133" refname="GPS_PL_4733_13-sc-2191244" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629133</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_4733_13-sc-2191244</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029669</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#71" center_name="The Wellcome Trust Sanger Institute" accession="ERX963867">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963867</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#71</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029681, constructed from sample accession ERS629134 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence GTGTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629134" refname="GPS_PL_4829_13-sc-2191245" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629134</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_4829_13-sc-2191245</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029681</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#72" center_name="The Wellcome Trust Sanger Institute" accession="ERX963868">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963868</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#72</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029693, constructed from sample accession ERS629135 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence GACGGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629135" refname="GPS_PL_4904_13-sc-2191246" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629135</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_4904_13-sc-2191246</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029693</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#73" center_name="The Wellcome Trust Sanger Institute" accession="ERX963869">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963869</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#73</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029610, constructed from sample accession ERS629136 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629136" refname="GPS_PL_5127_13-sc-2191247" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629136</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_5127_13-sc-2191247</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029610</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#74" center_name="The Wellcome Trust Sanger Institute" accession="ERX963870">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963870</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#74</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029622, constructed from sample accession ERS629137 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629137" refname="GPS_PL_5413_13-sc-2191248" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629137</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_5413_13-sc-2191248</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029622</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#75" center_name="The Wellcome Trust Sanger Institute" accession="ERX963871">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963871</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#75</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_2#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 13029634, constructed from sample accession ERS629138 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence GAATCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629138" refname="GPS_PL_5557_13-sc-2191249" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629138</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_5557_13-sc-2191249</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029634</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#76" center_name="The Wellcome Trust Sanger Institute" accession="ERX963872">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963872</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#76</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029646, constructed from sample accession ERS629139 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629139" refname="GPS_PL_5721_13-sc-2191250" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629139</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_5721_13-sc-2191250</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029646</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#77" center_name="The Wellcome Trust Sanger Institute" accession="ERX963873">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963873</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#77</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029658, constructed from sample accession ERS629140 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629140" refname="GPS_PL_5831_13-sc-2191251" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629140</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_5831_13-sc-2191251</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029658</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#78" center_name="The Wellcome Trust Sanger Institute" accession="ERX963874">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963874</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#78</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029670, constructed from sample accession ERS629141 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629141" refname="GPS_PL_5917_13-sc-2191252" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629141</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_5917_13-sc-2191252</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029670</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#79" center_name="The Wellcome Trust Sanger Institute" accession="ERX963875">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963875</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#79</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029682, constructed from sample accession ERS629142 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629142" refname="GPS_PL_25_14-sc-2191253" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629142</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_25_14-sc-2191253</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029682</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_3#1" center_name="The Wellcome Trust Sanger Institute" accession="ERX963876">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963876</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032454, constructed from sample accession ERS634569 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634569" refname="GPS_TH_BK_0235-sc-2191271" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634569</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0235-sc-2191271</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032454</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_5#15" center_name="The Wellcome Trust Sanger Institute" accession="ERX964072">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964072</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041624, constructed from sample accession ERS634760 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634760" refname="GPS_TH_BK_0693-sc-2191466" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634760</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0693-sc-2191466</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041624</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#16" center_name="The Wellcome Trust Sanger Institute" accession="ERX964073">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964073</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041636, constructed from sample accession ERS634762 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634762" refname="GPS_TH_BK_0696-sc-2191468" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634762</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0696-sc-2191468</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041636</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#17" center_name="The Wellcome Trust Sanger Institute" accession="ERX964074">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964074</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041553, constructed from sample accession ERS634763 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634763" refname="GPS_TH_BK_0697-sc-2191469" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634763</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0697-sc-2191469</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041553</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#18" center_name="The Wellcome Trust Sanger Institute" accession="ERX964075">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964075</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041565, constructed from sample accession ERS634765 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634765" refname="GPS_TH_BK_0701-sc-2191471" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634765</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0701-sc-2191471</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041565</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#19" center_name="The Wellcome Trust Sanger Institute" accession="ERX964076">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964076</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041577, constructed from sample accession ERS634766 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634766" refname="GPS_TH_BK_0702-sc-2191472" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634766</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0702-sc-2191472</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041577</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#20" center_name="The Wellcome Trust Sanger Institute" accession="ERX964077">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964077</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041589, constructed from sample accession ERS634767 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634767" refname="GPS_TH_BK_0704-sc-2191473" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634767</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0704-sc-2191473</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041589</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#21" center_name="The Wellcome Trust Sanger Institute" accession="ERX964078">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964078</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041601, constructed from sample accession ERS634769 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634769" refname="GPS_TH_BK_0706-sc-2191475" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634769</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0706-sc-2191475</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041601</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#22" center_name="The Wellcome Trust Sanger Institute" accession="ERX964079">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964079</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041613, constructed from sample accession ERS634770 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634770" refname="GPS_TH_BK_0707-sc-2191476" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634770</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0707-sc-2191476</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041613</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#23" center_name="The Wellcome Trust Sanger Institute" accession="ERX964080">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964080</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041625, constructed from sample accession ERS634772 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634772" refname="GPS_TH_BK_0708-sc-2191478" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634772</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0708-sc-2191478</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041625</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#24" center_name="The Wellcome Trust Sanger Institute" accession="ERX964081">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964081</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041637, constructed from sample accession ERS634773 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634773" refname="GPS_TH_BK_0709-sc-2191479" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634773</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0709-sc-2191479</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041637</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#25" center_name="The Wellcome Trust Sanger Institute" accession="ERX964082">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964082</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041554, constructed from sample accession ERS634774 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634774" refname="GPS_TH_BK_0710-sc-2191480" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634774</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0710-sc-2191480</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041554</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#26" center_name="The Wellcome Trust Sanger Institute" accession="ERX964083">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964083</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041566, constructed from sample accession ERS634775 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634775" refname="GPS_TH_BK_0712-sc-2191481" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634775</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0712-sc-2191481</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041566</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#27" center_name="The Wellcome Trust Sanger Institute" accession="ERX964084">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964084</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041578, constructed from sample accession ERS634776 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634776" refname="GPS_TH_BK_0713-sc-2191482" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634776</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0713-sc-2191482</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041578</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_3#2" center_name="The Wellcome Trust Sanger Institute" accession="ERX963877">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963877</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032466, constructed from sample accession ERS634570 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634570" refname="GPS_TH_BK_0236-sc-2191272" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634570</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0236-sc-2191272</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032466</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#3" center_name="The Wellcome Trust Sanger Institute" accession="ERX963878">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963878</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032478, constructed from sample accession ERS634571 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634571" refname="GPS_TH_BK_0239-sc-2191273" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634571</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0239-sc-2191273</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032478</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#4" center_name="The Wellcome Trust Sanger Institute" accession="ERX963879">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963879</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032490, constructed from sample accession ERS634572 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634572" refname="GPS_TH_BK_0250-sc-2191274" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634572</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0250-sc-2191274</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032490</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#5" center_name="The Wellcome Trust Sanger Institute" accession="ERX963880">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963880</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032502, constructed from sample accession ERS634573 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634573" refname="GPS_TH_BK_0253-sc-2191275" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634573</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0253-sc-2191275</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032502</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#6" center_name="The Wellcome Trust Sanger Institute" accession="ERX963881">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963881</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032514, constructed from sample accession ERS634574 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634574" refname="GPS_TH_BK_0254-sc-2191276" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634574</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0254-sc-2191276</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032514</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#7" center_name="The Wellcome Trust Sanger Institute" accession="ERX963882">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963882</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032526, constructed from sample accession ERS634575 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634575" refname="GPS_TH_BK_0256-sc-2191277" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634575</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0256-sc-2191277</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032526</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX963883">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963883</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032538, constructed from sample accession ERS634576 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634576" refname="GPS_TH_BK_0261-sc-2191278" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634576</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0261-sc-2191278</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032538</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#9" center_name="The Wellcome Trust Sanger Institute" accession="ERX963884">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963884</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032455, constructed from sample accession ERS634577 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634577" refname="GPS_TH_BK_0273-sc-2191279" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634577</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0273-sc-2191279</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032455</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#10" center_name="The Wellcome Trust Sanger Institute" accession="ERX963885">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963885</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032467, constructed from sample accession ERS634578 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634578" refname="GPS_TH_BK_0276-sc-2191280" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634578</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0276-sc-2191280</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032467</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#11" center_name="The Wellcome Trust Sanger Institute" accession="ERX963886">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963886</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032479, constructed from sample accession ERS634579 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634579" refname="GPS_TH_BK_0278-sc-2191281" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634579</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0278-sc-2191281</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032479</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#12" center_name="The Wellcome Trust Sanger Institute" accession="ERX963887">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963887</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032491, constructed from sample accession ERS634580 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634580" refname="GPS_TH_BK_0281-sc-2191282" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634580</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0281-sc-2191282</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032491</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#13" center_name="The Wellcome Trust Sanger Institute" accession="ERX963888">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963888</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032503, constructed from sample accession ERS634581 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634581" refname="GPS_TH_BK_0283-sc-2191283" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634581</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0283-sc-2191283</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032503</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#14" center_name="The Wellcome Trust Sanger Institute" accession="ERX963889">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963889</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032515, constructed from sample accession ERS634583 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634583" refname="GPS_TH_BK_0284-sc-2191285" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634583</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0284-sc-2191285</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032515</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_5#28" center_name="The Wellcome Trust Sanger Institute" accession="ERX964085">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964085</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041590, constructed from sample accession ERS634777 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634777" refname="GPS_TH_BK_0714-sc-2191483" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634777</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0714-sc-2191483</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041590</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#29" center_name="The Wellcome Trust Sanger Institute" accession="ERX964086">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964086</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041602, constructed from sample accession ERS634779 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634779" refname="GPS_TH_BK_0715-sc-2191485" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634779</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0715-sc-2191485</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041602</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#30" center_name="The Wellcome Trust Sanger Institute" accession="ERX964087">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964087</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041614, constructed from sample accession ERS634780 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634780" refname="GPS_TH_BK_0716-sc-2191486" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634780</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0716-sc-2191486</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041614</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX964088">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964088</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041626, constructed from sample accession ERS634781 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634781" refname="GPS_TH_BK_0717-sc-2191487" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634781</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0717-sc-2191487</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041626</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX964089">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964089</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041638, constructed from sample accession ERS634782 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634782" refname="GPS_TH_BK_0719-sc-2191489" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634782</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0719-sc-2191489</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041638</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX964090">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964090</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041555, constructed from sample accession ERS634783 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634783" refname="GPS_TH_BK_0720-sc-2191490" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634783</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0720-sc-2191490</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041555</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX964091">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964091</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041567, constructed from sample accession ERS634784 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634784" refname="GPS_TH_BK_0722-sc-2191491" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634784</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0722-sc-2191491</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041567</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX964092">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964092</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041579, constructed from sample accession ERS634785 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634785" refname="GPS_TH_BK_0723-sc-2191492" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634785</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0723-sc-2191492</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041579</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX964093">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964093</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041591, constructed from sample accession ERS634786 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634786" refname="GPS_TH_BK_0724-sc-2191493" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634786</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0724-sc-2191493</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041591</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX964094">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964094</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041603, constructed from sample accession ERS634787 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634787" refname="GPS_TH_BK_0725-sc-2191494" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634787</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0725-sc-2191494</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041603</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX964095">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964095</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041615, constructed from sample accession ERS634788 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634788" refname="GPS_TH_BK_0728-sc-2191495" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634788</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0728-sc-2191495</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041615</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#39" center_name="The Wellcome Trust Sanger Institute" accession="ERX964096">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964096</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#39</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041627, constructed from sample accession ERS634789 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634789" refname="GPS_TH_BK_0731-sc-2191496" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634789</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0731-sc-2191496</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041627</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#41" center_name="The Wellcome Trust Sanger Institute" accession="ERX964097">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964097</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#41</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041556, constructed from sample accession ERS634791 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634791" refname="GPS_TH_BK_0737-sc-2191498" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634791</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0737-sc-2191498</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041556</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_3#15" center_name="The Wellcome Trust Sanger Institute" accession="ERX963890">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963890</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032527, constructed from sample accession ERS634584 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634584" refname="GPS_TH_BK_0288-sc-2191286" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634584</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0288-sc-2191286</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032527</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#16" center_name="The Wellcome Trust Sanger Institute" accession="ERX963891">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963891</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032539, constructed from sample accession ERS634586 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634586" refname="GPS_TH_BK_0290-sc-2191288" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634586</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0290-sc-2191288</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032539</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#17" center_name="The Wellcome Trust Sanger Institute" accession="ERX963892">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963892</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032456, constructed from sample accession ERS634587 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634587" refname="GPS_TH_BK_0295-sc-2191289" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634587</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0295-sc-2191289</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032456</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#18" center_name="The Wellcome Trust Sanger Institute" accession="ERX963893">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963893</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032468, constructed from sample accession ERS634588 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634588" refname="GPS_TH_BK_0300-sc-2191290" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634588</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0300-sc-2191290</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032468</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#19" center_name="The Wellcome Trust Sanger Institute" accession="ERX963894">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963894</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032480, constructed from sample accession ERS634590 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634590" refname="GPS_TH_BK_0302-sc-2191292" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634590</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0302-sc-2191292</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032480</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#20" center_name="The Wellcome Trust Sanger Institute" accession="ERX963895">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963895</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032492, constructed from sample accession ERS634591 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634591" refname="GPS_TH_BK_0306-sc-2191293" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634591</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0306-sc-2191293</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032492</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#21" center_name="The Wellcome Trust Sanger Institute" accession="ERX963896">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963896</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032504, constructed from sample accession ERS634593 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634593" refname="GPS_TH_BK_0313-sc-2191295" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634593</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0313-sc-2191295</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032504</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#22" center_name="The Wellcome Trust Sanger Institute" accession="ERX963897">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963897</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032516, constructed from sample accession ERS634594 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634594" refname="GPS_TH_BK_0317-sc-2191296" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634594</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0317-sc-2191296</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032516</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#23" center_name="The Wellcome Trust Sanger Institute" accession="ERX963898">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963898</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032528, constructed from sample accession ERS634596 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634596" refname="GPS_TH_BK_0318-sc-2191298" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634596</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0318-sc-2191298</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032528</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#24" center_name="The Wellcome Trust Sanger Institute" accession="ERX963899">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963899</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032540, constructed from sample accession ERS634597 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634597" refname="GPS_TH_BK_0319-sc-2191299" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634597</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0319-sc-2191299</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032540</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#25" center_name="The Wellcome Trust Sanger Institute" accession="ERX963900">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963900</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032457, constructed from sample accession ERS634599 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634599" refname="GPS_TH_BK_0321-sc-2191301" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634599</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0321-sc-2191301</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032457</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#26" center_name="The Wellcome Trust Sanger Institute" accession="ERX963901">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963901</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032469, constructed from sample accession ERS634600 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634600" refname="GPS_TH_BK_0322-sc-2191302" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634600</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0322-sc-2191302</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032469</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#27" center_name="The Wellcome Trust Sanger Institute" accession="ERX963902">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963902</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032481, constructed from sample accession ERS634602 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634602" refname="GPS_TH_BK_0326-sc-2191304" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634602</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0326-sc-2191304</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032481</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_5#42" center_name="The Wellcome Trust Sanger Institute" accession="ERX964098">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964098</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#42</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041568, constructed from sample accession ERS634792 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634792" refname="GPS_TH_BK_0738-sc-2191499" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634792</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0738-sc-2191499</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041568</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#43" center_name="The Wellcome Trust Sanger Institute" accession="ERX964099">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964099</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#43</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#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 13041580, constructed from sample accession ERS634793 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634793" refname="GPS_TH_BK_0739-sc-2191500" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634793</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0739-sc-2191500</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041580</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_1#1" center_name="The Wellcome Trust Sanger Institute" accession="ERX963702">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963702</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029504, constructed from sample accession ERS628920 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628920" refname="GPS_PL_2798_08-sc-2191029" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628920</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_2798_08-sc-2191029</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029504</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#2" center_name="The Wellcome Trust Sanger Institute" accession="ERX963703">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963703</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029516, constructed from sample accession ERS628922 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628922" refname="GPS_PL_3594_08-sc-2191031" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628922</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_3594_08-sc-2191031</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029516</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#3" center_name="The Wellcome Trust Sanger Institute" accession="ERX963704">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963704</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029528, constructed from sample accession ERS628923 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628923" refname="GPS_PL_3635_08-sc-2191032" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628923</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_3635_08-sc-2191032</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029528</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#4" center_name="The Wellcome Trust Sanger Institute" accession="ERX963705">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963705</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029540, constructed from sample accession ERS628924 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628924" refname="GPS_PL_3791_08-sc-2191033" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628924</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_3791_08-sc-2191033</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029540</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#5" center_name="The Wellcome Trust Sanger Institute" accession="ERX963706">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963706</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029552, constructed from sample accession ERS628926 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628926" refname="GPS_PL_3949_08-sc-2191035" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628926</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_3949_08-sc-2191035</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029552</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#6" center_name="The Wellcome Trust Sanger Institute" accession="ERX963707">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963707</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029564, constructed from sample accession ERS628927 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628927" refname="GPS_PL_4036_08-sc-2191036" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628927</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_4036_08-sc-2191036</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029564</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_3#28" center_name="The Wellcome Trust Sanger Institute" accession="ERX963903">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963903</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032493, constructed from sample accession ERS634603 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634603" refname="GPS_TH_BK_0333-sc-2191305" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634603</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0333-sc-2191305</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032493</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#29" center_name="The Wellcome Trust Sanger Institute" accession="ERX963904">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963904</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032505, constructed from sample accession ERS634604 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634604" refname="GPS_TH_BK_0334-sc-2191306" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634604</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0334-sc-2191306</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032505</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#30" center_name="The Wellcome Trust Sanger Institute" accession="ERX963905">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963905</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032517, constructed from sample accession ERS634606 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634606" refname="GPS_TH_BK_0337-sc-2191308" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634606</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0337-sc-2191308</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032517</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX963906">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963906</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032529, constructed from sample accession ERS634607 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634607" refname="GPS_TH_BK_0338-sc-2191309" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634607</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0338-sc-2191309</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032529</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX963907">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963907</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032541, constructed from sample accession ERS634608 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634608" refname="GPS_TH_BK_0340-sc-2191310" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634608</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0340-sc-2191310</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032541</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX963908">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963908</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032458, constructed from sample accession ERS634610 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634610" refname="GPS_TH_BK_0344-sc-2191312" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634610</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0344-sc-2191312</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032458</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX963910">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963910</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032482, constructed from sample accession ERS634613 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634613" refname="GPS_TH_BK_0346-sc-2191315" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634613</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0346-sc-2191315</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032482</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX963911">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963911</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032494, constructed from sample accession ERS634614 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634614" refname="GPS_TH_BK_0350-sc-2191316" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634614</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0350-sc-2191316</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032494</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX963912">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963912</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032506, constructed from sample accession ERS634616 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634616" refname="GPS_TH_BK_0351-sc-2191318" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634616</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0351-sc-2191318</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032506</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX963913">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963913</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032518, constructed from sample accession ERS634617 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634617" refname="GPS_TH_BK_0353-sc-2191319" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634617</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0353-sc-2191319</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032518</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#39" center_name="The Wellcome Trust Sanger Institute" accession="ERX963914">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963914</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#39</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032530, constructed from sample accession ERS634619 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634619" refname="GPS_TH_BK_0355-sc-2191321" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634619</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0355-sc-2191321</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032530</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#40" center_name="The Wellcome Trust Sanger Institute" accession="ERX963915">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963915</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#40</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032542, constructed from sample accession ERS634620 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634620" refname="GPS_TH_BK_0361-sc-2191322" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634620</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0361-sc-2191322</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032542</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_1#7" center_name="The Wellcome Trust Sanger Institute" accession="ERX963708">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963708</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029576, constructed from sample accession ERS628929 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628929" refname="GPS_PL_4042_08-sc-2191038" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628929</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_4042_08-sc-2191038</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029576</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX963709">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963709</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029588, constructed from sample accession ERS628930 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628930" refname="GPS_PL_4238_08-sc-2191039" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628930</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_4238_08-sc-2191039</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029588</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#9" center_name="The Wellcome Trust Sanger Institute" accession="ERX963710">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963710</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029505, constructed from sample accession ERS628932 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628932" refname="GPS_PL_4428_08-sc-2191041" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628932</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_4428_08-sc-2191041</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029505</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#10" center_name="The Wellcome Trust Sanger Institute" accession="ERX963711">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963711</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029517, constructed from sample accession ERS628933 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628933" refname="GPS_PL_4466_08-sc-2191042" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628933</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_4466_08-sc-2191042</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029517</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#11" center_name="The Wellcome Trust Sanger Institute" accession="ERX963712">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963712</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029529, constructed from sample accession ERS628934 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628934" refname="GPS_PL_4726_08-sc-2191043" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628934</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_4726_08-sc-2191043</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029529</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#12" center_name="The Wellcome Trust Sanger Institute" accession="ERX963713">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963713</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029541, constructed from sample accession ERS628935 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628935" refname="GPS_PL_4962_08-sc-2191044" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628935</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_4962_08-sc-2191044</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029541</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#13" center_name="The Wellcome Trust Sanger Institute" accession="ERX963714">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963714</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029553, constructed from sample accession ERS628936 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628936" refname="GPS_PL_5008_08-sc-2191045" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628936</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_5008_08-sc-2191045</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029553</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#14" center_name="The Wellcome Trust Sanger Institute" accession="ERX963715">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963715</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029565, constructed from sample accession ERS628937 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628937" refname="GPS_PL_5205_08-sc-2191046" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628937</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_5205_08-sc-2191046</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029565</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#15" center_name="The Wellcome Trust Sanger Institute" accession="ERX963716">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963716</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029577, constructed from sample accession ERS628938 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628938" refname="GPS_PL_104_09-sc-2191047" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628938</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_104_09-sc-2191047</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029577</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#16" center_name="The Wellcome Trust Sanger Institute" accession="ERX963717">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963717</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029589, constructed from sample accession ERS628939 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628939" refname="GPS_PL_184_09-sc-2191048" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628939</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_184_09-sc-2191048</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029589</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#17" center_name="The Wellcome Trust Sanger Institute" accession="ERX963718">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963718</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029506, constructed from sample accession ERS628941 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628941" refname="GPS_PL_457_09-sc-2191050" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628941</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_457_09-sc-2191050</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029506</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#18" center_name="The Wellcome Trust Sanger Institute" accession="ERX963719">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963719</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029518, constructed from sample accession ERS628942 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628942" refname="GPS_PL_494_09-sc-2191051" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628942</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_494_09-sc-2191051</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029518</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#19" center_name="The Wellcome Trust Sanger Institute" accession="ERX963720">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963720</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029530, constructed from sample accession ERS628944 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628944" refname="GPS_PL_504_09-sc-2191053" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628944</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_504_09-sc-2191053</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029530</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_3#41" center_name="The Wellcome Trust Sanger Institute" accession="ERX963916">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963916</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#41</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032459, constructed from sample accession ERS634621 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634621" refname="GPS_TH_BK_0363-sc-2191323" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634621</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0363-sc-2191323</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032459</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#42" center_name="The Wellcome Trust Sanger Institute" accession="ERX963917">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963917</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#42</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032471, constructed from sample accession ERS634623 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634623" refname="GPS_TH_BK_0364-sc-2191325" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634623</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0364-sc-2191325</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032471</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#43" center_name="The Wellcome Trust Sanger Institute" accession="ERX963918">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963918</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#43</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032483, constructed from sample accession ERS634624 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634624" refname="GPS_TH_BK_0365-sc-2191326" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634624</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0365-sc-2191326</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032483</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#44" center_name="The Wellcome Trust Sanger Institute" accession="ERX963919">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963919</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#44</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032495, constructed from sample accession ERS634626 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634626" refname="GPS_TH_BK_0366-sc-2191328" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634626</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0366-sc-2191328</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032495</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#45" center_name="The Wellcome Trust Sanger Institute" accession="ERX963920">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963920</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#45</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032507, constructed from sample accession ERS634627 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634627" refname="GPS_TH_BK_0371-sc-2191329" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634627</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0371-sc-2191329</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032507</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#46" center_name="The Wellcome Trust Sanger Institute" accession="ERX963921">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963921</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#46</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032519, constructed from sample accession ERS634628 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634628" refname="GPS_TH_BK_0375-sc-2191330" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634628</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0375-sc-2191330</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032519</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#47" center_name="The Wellcome Trust Sanger Institute" accession="ERX963922">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963922</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#47</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032531, constructed from sample accession ERS634630 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634630" refname="GPS_TH_BK_0378-sc-2191332" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634630</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0378-sc-2191332</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032531</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#48" center_name="The Wellcome Trust Sanger Institute" accession="ERX963923">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963923</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#48</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032543, constructed from sample accession ERS634631 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634631" refname="GPS_TH_BK_0379-sc-2191333" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634631</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0379-sc-2191333</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032543</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#49" center_name="The Wellcome Trust Sanger Institute" accession="ERX963924">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963924</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#49</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032460, constructed from sample accession ERS634633 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634633" refname="GPS_TH_BK_0380-sc-2191335" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634633</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0380-sc-2191335</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032460</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#50" center_name="The Wellcome Trust Sanger Institute" accession="ERX963925">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963925</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#50</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032472, constructed from sample accession ERS634634 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634634" refname="GPS_TH_BK_0383-sc-2191336" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634634</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0383-sc-2191336</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032472</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#51" center_name="The Wellcome Trust Sanger Institute" accession="ERX963926">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963926</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#51</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032484, constructed from sample accession ERS634635 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634635" refname="GPS_TH_BK_0387-sc-2191337" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634635</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0387-sc-2191337</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032484</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#52" center_name="The Wellcome Trust Sanger Institute" accession="ERX963927">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963927</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#52</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032496, constructed from sample accession ERS634637 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634637" refname="GPS_TH_BK_0389-sc-2191339" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634637</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0389-sc-2191339</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032496</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#53" center_name="The Wellcome Trust Sanger Institute" accession="ERX963928">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963928</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#53</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032508, constructed from sample accession ERS634638 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634638" refname="GPS_TH_BK_0396-sc-2191340" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634638</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0396-sc-2191340</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032508</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_1#20" center_name="The Wellcome Trust Sanger Institute" accession="ERX963721">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963721</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029542, constructed from sample accession ERS628945 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628945" refname="GPS_PL_555_09-sc-2191054" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628945</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_555_09-sc-2191054</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029542</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#21" center_name="The Wellcome Trust Sanger Institute" accession="ERX963722">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963722</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029554, constructed from sample accession ERS628946 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628946" refname="GPS_PL_790_09-sc-2191055" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628946</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_790_09-sc-2191055</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029554</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#23" center_name="The Wellcome Trust Sanger Institute" accession="ERX963724">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963724</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029578, constructed from sample accession ERS628949 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628949" refname="GPS_PL_1775_09-sc-2191058" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628949</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_1775_09-sc-2191058</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029578</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#24" center_name="The Wellcome Trust Sanger Institute" accession="ERX963725">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963725</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029590, constructed from sample accession ERS628951 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628951" refname="GPS_PL_2089_09-sc-2191060" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628951</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_2089_09-sc-2191060</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029590</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#25" center_name="The Wellcome Trust Sanger Institute" accession="ERX963726">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963726</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029507, constructed from sample accession ERS628952 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628952" refname="GPS_PL_2314_09-sc-2191061" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628952</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_2314_09-sc-2191061</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029507</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#26" center_name="The Wellcome Trust Sanger Institute" accession="ERX963727">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963727</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029519, constructed from sample accession ERS628953 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628953" refname="GPS_PL_2916_09-sc-2191062" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628953</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_2916_09-sc-2191062</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029519</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#27" center_name="The Wellcome Trust Sanger Institute" accession="ERX963728">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963728</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029531, constructed from sample accession ERS628955 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628955" refname="GPS_PL_3328_09-sc-2191064" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628955</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_3328_09-sc-2191064</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029531</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#28" center_name="The Wellcome Trust Sanger Institute" accession="ERX963729">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963729</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029543, constructed from sample accession ERS628956 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628956" refname="GPS_PL_3543_09-sc-2191065" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628956</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_3543_09-sc-2191065</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029543</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#29" center_name="The Wellcome Trust Sanger Institute" accession="ERX963730">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963730</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029555, constructed from sample accession ERS628958 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628958" refname="GPS_PL_3680_09-sc-2191067" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628958</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_3680_09-sc-2191067</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029555</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#30" center_name="The Wellcome Trust Sanger Institute" accession="ERX963731">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963731</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029567, constructed from sample accession ERS628959 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628959" refname="GPS_PL_3700_09-sc-2191068" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628959</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_3700_09-sc-2191068</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029567</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX963732">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963732</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029579, constructed from sample accession ERS628960 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628960" refname="GPS_PL_4056_09-sc-2191069" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628960</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_4056_09-sc-2191069</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029579</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX963733">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963733</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029591, constructed from sample accession ERS628962 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628962" refname="GPS_PL_4980_09-sc-2191071" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628962</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_4980_09-sc-2191071</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029591</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_3#54" center_name="The Wellcome Trust Sanger Institute" accession="ERX963929">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963929</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#54</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032520, constructed from sample accession ERS634639 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634639" refname="GPS_TH_BK_0397-sc-2191341" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634639</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0397-sc-2191341</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032520</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#55" center_name="The Wellcome Trust Sanger Institute" accession="ERX963930">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963930</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#55</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032532, constructed from sample accession ERS634641 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634641" refname="GPS_TH_BK_0402-sc-2191343" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634641</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0402-sc-2191343</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032532</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#56" center_name="The Wellcome Trust Sanger Institute" accession="ERX963931">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963931</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#56</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032544, constructed from sample accession ERS634642 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634642" refname="GPS_TH_BK_0403-sc-2191344" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634642</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0403-sc-2191344</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032544</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#57" center_name="The Wellcome Trust Sanger Institute" accession="ERX963932">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963932</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#57</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032461, constructed from sample accession ERS634643 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634643" refname="GPS_TH_BK_0406-sc-2191345" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634643</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0406-sc-2191345</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032461</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#58" center_name="The Wellcome Trust Sanger Institute" accession="ERX963933">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963933</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#58</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032473, constructed from sample accession ERS634645 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634645" refname="GPS_TH_BK_0407-sc-2191347" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634645</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0407-sc-2191347</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032473</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#59" center_name="The Wellcome Trust Sanger Institute" accession="ERX963934">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963934</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#59</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_3#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 13032485, constructed from sample accession ERS634646 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634646" refname="GPS_TH_BK_0410-sc-2191348" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634646</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0410-sc-2191348</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032485</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#60" center_name="The Wellcome Trust Sanger Institute" accession="ERX963935">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963935</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#60</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032497, constructed from sample accession ERS634647 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634647" refname="GPS_TH_BK_0413-sc-2191349" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634647</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0413-sc-2191349</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032497</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#61" center_name="The Wellcome Trust Sanger Institute" accession="ERX963936">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963936</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#61</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032509, constructed from sample accession ERS634649 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634649" refname="GPS_TH_BK_0415-sc-2191351" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634649</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0415-sc-2191351</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032509</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#62" center_name="The Wellcome Trust Sanger Institute" accession="ERX963937">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963937</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#62</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032521, constructed from sample accession ERS634650 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634650" refname="GPS_TH_BK_0417-sc-2191352" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634650</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0417-sc-2191352</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032521</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#63" center_name="The Wellcome Trust Sanger Institute" accession="ERX963938">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963938</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#63</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032533, constructed from sample accession ERS634652 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634652" refname="GPS_TH_BK_0427-sc-2191354" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634652</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0427-sc-2191354</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032533</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#64" center_name="The Wellcome Trust Sanger Institute" accession="ERX963939">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963939</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#64</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032545, constructed from sample accession ERS634653 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634653" refname="GPS_TH_BK_0428-sc-2191355" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634653</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0428-sc-2191355</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032545</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#65" center_name="The Wellcome Trust Sanger Institute" accession="ERX963940">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963940</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#65</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032462, constructed from sample accession ERS634655 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634655" refname="GPS_TH_BK_0434-sc-2191357" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634655</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0434-sc-2191357</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032462</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#66" center_name="The Wellcome Trust Sanger Institute" accession="ERX963941">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963941</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#66</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032474, constructed from sample accession ERS634656 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634656" refname="GPS_TH_BK_0436-sc-2191358" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634656</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0436-sc-2191358</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032474</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_1#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX963734">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963734</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029508, constructed from sample accession ERS628963 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628963" refname="GPS_PL_5016_09-sc-2191072" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628963</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_5016_09-sc-2191072</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029508</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX963735">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963735</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029520, constructed from sample accession ERS628965 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628965" refname="GPS_PL_5073_09-sc-2191074" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628965</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_5073_09-sc-2191074</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029520</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX963736">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963736</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029532, constructed from sample accession ERS628966 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628966" refname="GPS_PL_5099_09-sc-2191075" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628966</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_5099_09-sc-2191075</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029532</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX963737">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963737</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029544, constructed from sample accession ERS628968 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628968" refname="GPS_PL_5697_09-sc-2191077" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628968</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_5697_09-sc-2191077</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029544</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX963738">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963738</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029556, constructed from sample accession ERS628969 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628969" refname="GPS_PL_5910_09-sc-2191078" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628969</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_5910_09-sc-2191078</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029556</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX963739">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963739</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029568, constructed from sample accession ERS628970 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628970" refname="GPS_PL_6002_09-sc-2191079" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628970</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_6002_09-sc-2191079</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029568</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#39" center_name="The Wellcome Trust Sanger Institute" accession="ERX963740">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963740</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#39</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029580, constructed from sample accession ERS628972 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628972" refname="GPS_PL_6349_09-sc-2191081" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628972</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_6349_09-sc-2191081</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029580</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#40" center_name="The Wellcome Trust Sanger Institute" accession="ERX963741">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963741</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#40</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029592, constructed from sample accession ERS628973 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628973" refname="GPS_PL_6361_09-sc-2191082" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628973</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_6361_09-sc-2191082</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029592</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#41" center_name="The Wellcome Trust Sanger Institute" accession="ERX963742">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963742</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#41</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029509, constructed from sample accession ERS628975 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628975" refname="GPS_PL_6403_09-sc-2191084" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628975</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_6403_09-sc-2191084</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029509</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#42" center_name="The Wellcome Trust Sanger Institute" accession="ERX963743">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963743</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#42</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029521, constructed from sample accession ERS628976 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628976" refname="GPS_PL_6524_09-sc-2191085" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628976</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_6524_09-sc-2191085</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029521</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#43" center_name="The Wellcome Trust Sanger Institute" accession="ERX963744">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963744</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#43</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029533, constructed from sample accession ERS628978 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628978" refname="GPS_PL_6534_09-sc-2191087" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628978</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_6534_09-sc-2191087</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029533</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#44" center_name="The Wellcome Trust Sanger Institute" accession="ERX963745">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963745</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#44</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029545, constructed from sample accession ERS628979 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628979" refname="GPS_PL_6579_09-sc-2191088" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628979</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_6579_09-sc-2191088</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029545</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#45" center_name="The Wellcome Trust Sanger Institute" accession="ERX963746">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963746</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#45</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029557, constructed from sample accession ERS628981 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628981" refname="GPS_PL_543_10-sc-2191090" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628981</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_543_10-sc-2191090</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029557</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_3#67" center_name="The Wellcome Trust Sanger Institute" accession="ERX963942">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963942</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#67</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032486, constructed from sample accession ERS634657 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634657" refname="GPS_TH_BK_0437-sc-2191359" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634657</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0437-sc-2191359</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032486</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#68" center_name="The Wellcome Trust Sanger Institute" accession="ERX963943">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963943</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#68</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032498, constructed from sample accession ERS634659 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634659" refname="GPS_TH_BK_0442-sc-2191361" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634659</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0442-sc-2191361</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032498</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#69" center_name="The Wellcome Trust Sanger Institute" accession="ERX963944">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963944</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#69</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032510, constructed from sample accession ERS634660 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634660" refname="GPS_TH_BK_0455-sc-2191362" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634660</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0455-sc-2191362</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032510</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#70" center_name="The Wellcome Trust Sanger Institute" accession="ERX963945">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963945</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#70</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032522, constructed from sample accession ERS634662 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634662" refname="GPS_TH_BK_0456-sc-2191364" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634662</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0456-sc-2191364</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032522</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#71" center_name="The Wellcome Trust Sanger Institute" accession="ERX963946">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963946</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#71</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_3#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 13032534, constructed from sample accession ERS634663 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence GTGTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634663" refname="GPS_TH_BK_0461-sc-2191365" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634663</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0461-sc-2191365</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032534</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#72" center_name="The Wellcome Trust Sanger Institute" accession="ERX963947">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963947</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#72</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032546, constructed from sample accession ERS634664 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence GACGGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634664" refname="GPS_TH_BK_0464-sc-2191366" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634664</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0464-sc-2191366</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032546</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#73" center_name="The Wellcome Trust Sanger Institute" accession="ERX963948">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963948</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#73</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032463, constructed from sample accession ERS634666 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634666" refname="GPS_TH_BK_0466-sc-2191368" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634666</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0466-sc-2191368</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032463</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#74" center_name="The Wellcome Trust Sanger Institute" accession="ERX963949">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963949</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#74</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032475, constructed from sample accession ERS634667 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634667" refname="GPS_TH_BK_0467-sc-2191369" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634667</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0467-sc-2191369</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032475</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#75" center_name="The Wellcome Trust Sanger Institute" accession="ERX963950">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963950</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#75</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032487, constructed from sample accession ERS634669 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence GAATCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634669" refname="GPS_TH_BK_0468-sc-2191371" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634669</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0468-sc-2191371</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032487</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#76" center_name="The Wellcome Trust Sanger Institute" accession="ERX963951">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963951</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#76</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032499, constructed from sample accession ERS634670 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634670" refname="GPS_TH_BK_0469-sc-2191372" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634670</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0469-sc-2191372</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032499</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#77" center_name="The Wellcome Trust Sanger Institute" accession="ERX963952">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963952</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#77</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032511, constructed from sample accession ERS634671 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634671" refname="GPS_TH_BK_0470-sc-2191373" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634671</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0470-sc-2191373</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032511</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#78" center_name="The Wellcome Trust Sanger Institute" accession="ERX963953">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963953</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#78</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032523, constructed from sample accession ERS634673 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634673" refname="GPS_TH_BK_0475-sc-2191375" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634673</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0475-sc-2191375</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032523</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#79" center_name="The Wellcome Trust Sanger Institute" accession="ERX963954">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963954</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#79</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032535, constructed from sample accession ERS634674 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634674" refname="GPS_TH_BK_0477-sc-2191376" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634674</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0477-sc-2191376</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032535</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_1#46" center_name="The Wellcome Trust Sanger Institute" accession="ERX963747">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963747</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#46</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029569, constructed from sample accession ERS628982 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628982" refname="GPS_PL_648_10-sc-2191091" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628982</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_648_10-sc-2191091</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029569</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#47" center_name="The Wellcome Trust Sanger Institute" accession="ERX963748">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963748</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#47</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029581, constructed from sample accession ERS628984 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628984" refname="GPS_PL_717_10-sc-2191093" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628984</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_717_10-sc-2191093</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029581</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#48" center_name="The Wellcome Trust Sanger Institute" accession="ERX963749">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963749</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#48</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029593, constructed from sample accession ERS628985 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628985" refname="GPS_PL_781_10-sc-2191094" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628985</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_781_10-sc-2191094</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029593</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#49" center_name="The Wellcome Trust Sanger Institute" accession="ERX963750">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963750</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#49</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029510, constructed from sample accession ERS628987 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628987" refname="GPS_PL_782_10-sc-2191096" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628987</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_782_10-sc-2191096</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029510</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#50" center_name="The Wellcome Trust Sanger Institute" accession="ERX963751">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963751</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#50</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029522, constructed from sample accession ERS628988 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628988" refname="GPS_PL_1322_10-sc-2191097" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628988</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_1322_10-sc-2191097</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029522</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#51" center_name="The Wellcome Trust Sanger Institute" accession="ERX963752">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963752</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#51</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029534, constructed from sample accession ERS628989 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628989" refname="GPS_PL_1355_10-sc-2191098" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628989</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_1355_10-sc-2191098</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029534</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#52" center_name="The Wellcome Trust Sanger Institute" accession="ERX963753">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963753</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#52</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029546, constructed from sample accession ERS628991 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628991" refname="GPS_PL_1444_10-sc-2191100" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628991</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_1444_10-sc-2191100</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029546</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#53" center_name="The Wellcome Trust Sanger Institute" accession="ERX963754">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963754</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#53</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029558, constructed from sample accession ERS628992 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628992" refname="GPS_PL_1532_10-sc-2191101" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628992</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_1532_10-sc-2191101</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029558</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#54" center_name="The Wellcome Trust Sanger Institute" accession="ERX963755">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963755</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#54</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029570, constructed from sample accession ERS628994 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628994" refname="GPS_PL_1533_10-sc-2191103" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628994</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_1533_10-sc-2191103</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029570</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#55" center_name="The Wellcome Trust Sanger Institute" accession="ERX963756">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963756</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#55</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029582, constructed from sample accession ERS628995 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628995" refname="GPS_PL_1609_10-sc-2191104" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628995</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_1609_10-sc-2191104</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029582</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#56" center_name="The Wellcome Trust Sanger Institute" accession="ERX963757">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963757</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#56</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029594, constructed from sample accession ERS628996 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628996" refname="GPS_PL_1710_10-sc-2191105" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628996</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_1710_10-sc-2191105</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029594</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#57" center_name="The Wellcome Trust Sanger Institute" accession="ERX963758">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963758</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#57</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029511, constructed from sample accession ERS628998 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628998" refname="GPS_PL_1736_10-sc-2191107" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628998</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_1736_10-sc-2191107</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029511</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#58" center_name="The Wellcome Trust Sanger Institute" accession="ERX963759">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963759</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#58</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029523, constructed from sample accession ERS628999 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS628999" refname="GPS_PL_1884_10-sc-2191108" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS628999</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_1884_10-sc-2191108</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029523</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_3#80" center_name="The Wellcome Trust Sanger Institute" accession="ERX963955">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963955</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#80</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032547, constructed from sample accession ERS634675 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence GTCGCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634675" refname="GPS_TH_BK_0478-sc-2191377" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634675</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0478-sc-2191377</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032547</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#81" center_name="The Wellcome Trust Sanger Institute" accession="ERX963956">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963956</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#81</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032464, constructed from sample accession ERS634676 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634676" refname="GPS_TH_BK_0482-sc-2191378" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634676</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0482-sc-2191378</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032464</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#82" center_name="The Wellcome Trust Sanger Institute" accession="ERX963957">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963957</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#82</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032476, constructed from sample accession ERS634677 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634677" refname="GPS_TH_BK_0484-sc-2191379" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634677</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0484-sc-2191379</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032476</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#83" center_name="The Wellcome Trust Sanger Institute" accession="ERX963958">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963958</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#83</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032488, constructed from sample accession ERS634678 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence GCTCCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634678" refname="GPS_TH_BK_0486-sc-2191380" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634678</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0486-sc-2191380</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032488</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#84" center_name="The Wellcome Trust Sanger Institute" accession="ERX963959">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963959</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#84</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_3#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 13032500, constructed from sample accession ERS634679 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence GTAAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634679" refname="GPS_TH_BK_0487-sc-2191381" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634679</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0487-sc-2191381</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032500</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#85" center_name="The Wellcome Trust Sanger Institute" accession="ERX963960">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963960</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#85</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032512, constructed from sample accession ERS634681 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence GAGGATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634681" refname="GPS_TH_BK_0489-sc-2191383" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634681</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0489-sc-2191383</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032512</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#86" center_name="The Wellcome Trust Sanger Institute" accession="ERX963961">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963961</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#86</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032524, constructed from sample accession ERS634682 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence GTTGTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634682" refname="GPS_TH_BK_0491-sc-2191384" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634682</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0491-sc-2191384</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032524</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#87" center_name="The Wellcome Trust Sanger Institute" accession="ERX963962">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963962</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#87</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032536, constructed from sample accession ERS634684 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence GGATTAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634684" refname="GPS_TH_BK_0492-sc-2191386" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634684</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0492-sc-2191386</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032536</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#88" center_name="The Wellcome Trust Sanger Institute" accession="ERX963963">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963963</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#88</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032548, constructed from sample accession ERS634685 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence GATAGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634685" refname="GPS_TH_BK_0497-sc-2191387" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634685</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0497-sc-2191387</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032548</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#89" center_name="The Wellcome Trust Sanger Institute" accession="ERX963964">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963964</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#89</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032465, constructed from sample accession ERS634687 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence GTGTGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634687" refname="GPS_TH_BK_0499-sc-2191389" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634687</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0499-sc-2191389</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032465</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#90" center_name="The Wellcome Trust Sanger Institute" accession="ERX963965">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963965</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#90</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032477, constructed from sample accession ERS634688 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence GCAATCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634688" refname="GPS_TH_BK_0503-sc-2191390" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634688</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0503-sc-2191390</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032477</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_3#91" center_name="The Wellcome Trust Sanger Institute" accession="ERX963966">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963966</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_3#91</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032489, constructed from sample accession ERS634690 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_3).  This submission includes reads tagged with the sequence GACCTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634690" refname="GPS_TH_BK_0504-sc-2191392" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634690</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0504-sc-2191392</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032489</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" 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_15682_4#1" center_name="The Wellcome Trust Sanger Institute" accession="ERX963967">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963967</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032745, constructed from sample accession ERS634691 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634691" refname="GPS_TH_BK_0505-sc-2191393" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634691</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0505-sc-2191393</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032745</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_1#59" center_name="The Wellcome Trust Sanger Institute" accession="ERX963760">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963760</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#59</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029535, constructed from sample accession ERS629001 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629001" refname="GPS_PL_2009_10-sc-2191110" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629001</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_2009_10-sc-2191110</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029535</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#60" center_name="The Wellcome Trust Sanger Institute" accession="ERX963761">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963761</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#60</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029547, constructed from sample accession ERS629002 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629002" refname="GPS_PL_2133_10-sc-2191111" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629002</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_2133_10-sc-2191111</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029547</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#61" center_name="The Wellcome Trust Sanger Institute" accession="ERX963762">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963762</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#61</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029559, constructed from sample accession ERS629003 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629003" refname="GPS_PL_2333_10-sc-2191112" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629003</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_2333_10-sc-2191112</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029559</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#62" center_name="The Wellcome Trust Sanger Institute" accession="ERX963763">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963763</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#62</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029571, constructed from sample accession ERS629005 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629005" refname="GPS_PL_2349_10-sc-2191114" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629005</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_2349_10-sc-2191114</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029571</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#63" center_name="The Wellcome Trust Sanger Institute" accession="ERX963764">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963764</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#63</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029583, constructed from sample accession ERS629006 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629006" refname="GPS_PL_3682_10-sc-2191115" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629006</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_3682_10-sc-2191115</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029583</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#64" center_name="The Wellcome Trust Sanger Institute" accession="ERX963765">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963765</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#64</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029595, constructed from sample accession ERS629008 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629008" refname="GPS_PL_3775_10-sc-2191117" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629008</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_3775_10-sc-2191117</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029595</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#65" center_name="The Wellcome Trust Sanger Institute" accession="ERX963766">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963766</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#65</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029512, constructed from sample accession ERS629009 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629009" refname="GPS_PL_4142_10-sc-2191118" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629009</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_4142_10-sc-2191118</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029512</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#66" center_name="The Wellcome Trust Sanger Institute" accession="ERX963767">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963767</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#66</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029524, constructed from sample accession ERS629011 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629011" refname="GPS_PL_5992_10-sc-2191120" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629011</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_5992_10-sc-2191120</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029524</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#67" center_name="The Wellcome Trust Sanger Institute" accession="ERX963768">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963768</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#67</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029536, constructed from sample accession ERS629012 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629012" refname="GPS_PL_6439_10-sc-2191121" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629012</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_6439_10-sc-2191121</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029536</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#68" center_name="The Wellcome Trust Sanger Institute" accession="ERX963769">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963769</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#68</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029548, constructed from sample accession ERS629014 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629014" refname="GPS_PL_7912_10-sc-2191123" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629014</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_7912_10-sc-2191123</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029548</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#69" center_name="The Wellcome Trust Sanger Institute" accession="ERX963770">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963770</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#69</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029560, constructed from sample accession ERS629015 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629015" refname="GPS_PL_7973_10-sc-2191124" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629015</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_7973_10-sc-2191124</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029560</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#70" center_name="The Wellcome Trust Sanger Institute" accession="ERX963771">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963771</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#70</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029572, constructed from sample accession ERS629016 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629016" refname="GPS_PL_8030_10-sc-2191125" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629016</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_8030_10-sc-2191125</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029572</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#71" center_name="The Wellcome Trust Sanger Institute" accession="ERX963772">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963772</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#71</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029584, constructed from sample accession ERS629018 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence GTGTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629018" refname="GPS_PL_8047_10-sc-2191127" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629018</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_8047_10-sc-2191127</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029584</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_4#2" center_name="The Wellcome Trust Sanger Institute" accession="ERX963968">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963968</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032757, constructed from sample accession ERS634692 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634692" refname="GPS_TH_BK_0506-sc-2191394" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634692</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0506-sc-2191394</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032757</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#3" center_name="The Wellcome Trust Sanger Institute" accession="ERX963969">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963969</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032769, constructed from sample accession ERS634694 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634694" refname="GPS_TH_BK_0507-sc-2191396" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634694</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0507-sc-2191396</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032769</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#4" center_name="The Wellcome Trust Sanger Institute" accession="ERX963970">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963970</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032781, constructed from sample accession ERS634582 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634582" refname="GPS_TH_BK_0508-sc-2191284" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634582</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0508-sc-2191284</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032781</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#5" center_name="The Wellcome Trust Sanger Institute" accession="ERX963971">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963971</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032799, constructed from sample accession ERS634585 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634585" refname="GPS_TH_BK_0509-sc-2191287" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634585</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0509-sc-2191287</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032799</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#6" center_name="The Wellcome Trust Sanger Institute" accession="ERX963972">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963972</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032822, constructed from sample accession ERS634589 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634589" refname="GPS_TH_BK_0510-sc-2191291" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634589</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0510-sc-2191291</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032822</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#7" center_name="The Wellcome Trust Sanger Institute" accession="ERX963973">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963973</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032843, constructed from sample accession ERS634592 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634592" refname="GPS_TH_BK_0511-sc-2191294" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634592</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0511-sc-2191294</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032843</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX963974">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963974</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032866, constructed from sample accession ERS634595 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634595" refname="GPS_TH_BK_0515-sc-2191297" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634595</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0515-sc-2191297</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032866</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#9" center_name="The Wellcome Trust Sanger Institute" accession="ERX963975">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963975</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032746, constructed from sample accession ERS634598 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634598" refname="GPS_TH_BK_0516-sc-2191300" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634598</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0516-sc-2191300</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032746</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#10" center_name="The Wellcome Trust Sanger Institute" accession="ERX963976">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963976</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032758, constructed from sample accession ERS634601 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634601" refname="GPS_TH_BK_0517-sc-2191303" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634601</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0517-sc-2191303</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032758</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#11" center_name="The Wellcome Trust Sanger Institute" accession="ERX963977">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963977</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032770, constructed from sample accession ERS634605 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634605" refname="GPS_TH_BK_0518-sc-2191307" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634605</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0518-sc-2191307</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032770</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#12" center_name="The Wellcome Trust Sanger Institute" accession="ERX963978">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963978</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032782, constructed from sample accession ERS634609 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634609" refname="GPS_TH_BK_0519-sc-2191311" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634609</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0519-sc-2191311</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032782</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#13" center_name="The Wellcome Trust Sanger Institute" accession="ERX963979">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963979</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032801, constructed from sample accession ERS634612 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634612" refname="GPS_TH_BK_0520-sc-2191314" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634612</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0520-sc-2191314</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032801</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#14" center_name="The Wellcome Trust Sanger Institute" accession="ERX963980">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963980</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032824, constructed from sample accession ERS634615 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634615" refname="GPS_TH_BK_0521-sc-2191317" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634615</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0521-sc-2191317</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032824</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_1#72" center_name="The Wellcome Trust Sanger Institute" accession="ERX963773">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963773</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#72</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029596, constructed from sample accession ERS629019 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence GACGGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629019" refname="GPS_PL_8598_10-sc-2191128" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629019</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_8598_10-sc-2191128</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029596</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#73" center_name="The Wellcome Trust Sanger Institute" accession="ERX963774">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963774</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#73</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029513, constructed from sample accession ERS629021 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629021" refname="GPS_PL_8668_10-sc-2191130" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629021</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_8668_10-sc-2191130</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029513</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#74" center_name="The Wellcome Trust Sanger Institute" accession="ERX963775">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963775</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#74</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029525, constructed from sample accession ERS629022 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629022" refname="GPS_PL_9257_10-sc-2191131" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629022</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_9257_10-sc-2191131</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029525</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#75" center_name="The Wellcome Trust Sanger Institute" accession="ERX963776">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963776</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#75</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029537, constructed from sample accession ERS629023 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence GAATCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629023" refname="GPS_PL_210_11-sc-2191132" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629023</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_210_11-sc-2191132</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029537</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#76" center_name="The Wellcome Trust Sanger Institute" accession="ERX963777">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963777</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#76</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029549, constructed from sample accession ERS629025 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629025" refname="GPS_PL_430_11-sc-2191134" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629025</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_430_11-sc-2191134</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029549</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#77" center_name="The Wellcome Trust Sanger Institute" accession="ERX963778">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963778</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#77</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029561, constructed from sample accession ERS629026 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629026" refname="GPS_PL_702_11-sc-2191135" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629026</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_702_11-sc-2191135</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029561</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#78" center_name="The Wellcome Trust Sanger Institute" accession="ERX963779">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963779</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#78</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029573, constructed from sample accession ERS629028 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629028" refname="GPS_PL_708_11-sc-2191137" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629028</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_708_11-sc-2191137</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029573</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#79" center_name="The Wellcome Trust Sanger Institute" accession="ERX963780">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963780</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#79</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029585, constructed from sample accession ERS629029 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629029" refname="GPS_PL_727_11-sc-2191138" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629029</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_727_11-sc-2191138</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029585</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#80" center_name="The Wellcome Trust Sanger Institute" accession="ERX963781">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963781</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#80</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029597, constructed from sample accession ERS629030 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence GTCGCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629030" refname="GPS_PL_807_11-sc-2191139" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629030</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_807_11-sc-2191139</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029597</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#81" center_name="The Wellcome Trust Sanger Institute" accession="ERX963782">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963782</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#81</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029514, constructed from sample accession ERS629032 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629032" refname="GPS_PL_951_11-sc-2191141" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629032</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_951_11-sc-2191141</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029514</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#82" center_name="The Wellcome Trust Sanger Institute" accession="ERX963783">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963783</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#82</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029526, constructed from sample accession ERS629033 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629033" refname="GPS_PL_1011_11-sc-2191142" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629033</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_1011_11-sc-2191142</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029526</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#83" center_name="The Wellcome Trust Sanger Institute" accession="ERX963784">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963784</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#83</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029538, constructed from sample accession ERS629035 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence GCTCCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629035" refname="GPS_PL_1126_11-sc-2191144" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629035</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_1126_11-sc-2191144</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029538</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#84" center_name="The Wellcome Trust Sanger Institute" accession="ERX963785">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963785</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#84</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029550, constructed from sample accession ERS629036 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence GTAAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629036" refname="GPS_PL_1236_11-sc-2191145" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629036</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_1236_11-sc-2191145</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029550</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_4#15" center_name="The Wellcome Trust Sanger Institute" accession="ERX963981">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963981</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032845, constructed from sample accession ERS634618 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634618" refname="GPS_TH_BK_0522-sc-2191320" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634618</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0522-sc-2191320</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032845</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#16" center_name="The Wellcome Trust Sanger Institute" accession="ERX963982">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963982</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032868, constructed from sample accession ERS634622 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634622" refname="GPS_TH_BK_0524-sc-2191324" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634622</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0524-sc-2191324</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032868</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#17" center_name="The Wellcome Trust Sanger Institute" accession="ERX963983">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963983</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032747, constructed from sample accession ERS634625 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634625" refname="GPS_TH_BK_0525-sc-2191327" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634625</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0525-sc-2191327</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032747</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#18" center_name="The Wellcome Trust Sanger Institute" accession="ERX963984">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963984</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032759, constructed from sample accession ERS634629 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634629" refname="GPS_TH_BK_0526-sc-2191331" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634629</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0526-sc-2191331</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032759</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#19" center_name="The Wellcome Trust Sanger Institute" accession="ERX963985">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963985</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032771, constructed from sample accession ERS634632 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634632" refname="GPS_TH_BK_0528-sc-2191334" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634632</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0528-sc-2191334</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032771</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#20" center_name="The Wellcome Trust Sanger Institute" accession="ERX963986">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963986</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032783, constructed from sample accession ERS634636 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634636" refname="GPS_TH_BK_0529-sc-2191338" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634636</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0529-sc-2191338</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032783</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#21" center_name="The Wellcome Trust Sanger Institute" accession="ERX963987">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963987</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032803, constructed from sample accession ERS634640 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634640" refname="GPS_TH_BK_0530-sc-2191342" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634640</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0530-sc-2191342</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032803</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#22" center_name="The Wellcome Trust Sanger Institute" accession="ERX963988">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963988</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032825, constructed from sample accession ERS634644 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634644" refname="GPS_TH_BK_0532-sc-2191346" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634644</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0532-sc-2191346</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032825</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#23" center_name="The Wellcome Trust Sanger Institute" accession="ERX963989">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963989</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032847, constructed from sample accession ERS634648 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634648" refname="GPS_TH_BK_0533-sc-2191350" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634648</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0533-sc-2191350</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032847</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#24" center_name="The Wellcome Trust Sanger Institute" accession="ERX963990">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963990</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032870, constructed from sample accession ERS634651 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634651" refname="GPS_TH_BK_0534-sc-2191353" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634651</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0534-sc-2191353</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032870</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#26" center_name="The Wellcome Trust Sanger Institute" accession="ERX963992">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963992</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032760, constructed from sample accession ERS634658 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634658" refname="GPS_TH_BK_0539-sc-2191360" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634658</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0539-sc-2191360</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032760</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#27" center_name="The Wellcome Trust Sanger Institute" accession="ERX963993">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963993</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032772, constructed from sample accession ERS634661 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634661" refname="GPS_TH_BK_0540-sc-2191363" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634661</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0540-sc-2191363</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032772</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_1#85" center_name="The Wellcome Trust Sanger Institute" accession="ERX963786">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963786</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#85</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029562, constructed from sample accession ERS629038 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence GAGGATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629038" refname="GPS_PL_1322_11-sc-2191147" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629038</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_1322_11-sc-2191147</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029562</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#86" center_name="The Wellcome Trust Sanger Institute" accession="ERX963787">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963787</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#86</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029574, constructed from sample accession ERS629039 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence GTTGTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629039" refname="GPS_PL_1336_11-sc-2191148" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629039</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_1336_11-sc-2191148</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029574</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#87" center_name="The Wellcome Trust Sanger Institute" accession="ERX963788">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963788</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#87</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029586, constructed from sample accession ERS629040 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence GGATTAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629040" refname="GPS_PL_1655_11-sc-2191149" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629040</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_1655_11-sc-2191149</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029586</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#88" center_name="The Wellcome Trust Sanger Institute" accession="ERX963789">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963789</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#88</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029598, constructed from sample accession ERS629042 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence GATAGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629042" refname="GPS_PL_1729_11-sc-2191151" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629042</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_1729_11-sc-2191151</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029598</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#89" center_name="The Wellcome Trust Sanger Institute" accession="ERX963790">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963790</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#89</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029515, constructed from sample accession ERS629043 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence GTGTGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629043" refname="GPS_PL_1736_11-sc-2191152" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629043</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_1736_11-sc-2191152</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029515</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#90" center_name="The Wellcome Trust Sanger Institute" accession="ERX963791">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963791</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#90</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029527, constructed from sample accession ERS629045 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence GCAATCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629045" refname="GPS_PL_1749_11-sc-2191154" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629045</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_1749_11-sc-2191154</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029527</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#91" center_name="The Wellcome Trust Sanger Institute" accession="ERX963792">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963792</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#91</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029539, constructed from sample accession ERS629046 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence GACCTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629046" refname="GPS_PL_4220_11-sc-2191155" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629046</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_4220_11-sc-2191155</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029539</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#92" center_name="The Wellcome Trust Sanger Institute" accession="ERX963793">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963793</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#92</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029551, constructed from sample accession ERS629048 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence GCCTGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629048" refname="GPS_PL_4588_11-sc-2191157" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629048</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_4588_11-sc-2191157</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029551</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#93" center_name="The Wellcome Trust Sanger Institute" accession="ERX963794">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963794</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#93</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029563, constructed from sample accession ERS629049 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence GCACTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629049" refname="GPS_PL_4608_11-sc-2191158" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629049</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_4608_11-sc-2191158</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029563</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#94" center_name="The Wellcome Trust Sanger Institute" accession="ERX963795">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963795</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#94</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029575, constructed from sample accession ERS629051 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence GCTAACTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629051" refname="GPS_PL_5540_11-sc-2191160" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629051</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_5540_11-sc-2191160</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029575</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_1#95" center_name="The Wellcome Trust Sanger Institute" accession="ERX963796">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963796</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_1#95</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_1#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 13029587, constructed from sample accession ERS629052 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_1).  This submission includes reads tagged with the sequence GATTCATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629052" refname="GPS_PL_8909_11-sc-2191161" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629052</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_8909_11-sc-2191161</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029587</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" 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_15682_2#1" center_name="The Wellcome Trust Sanger Institute" accession="ERX963797">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963797</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029601, constructed from sample accession ERS629064 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629064" refname="GPS_PL_9065_11-sc-2191175" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629064</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_9065_11-sc-2191175</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029601</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_2#2" center_name="The Wellcome Trust Sanger Institute" accession="ERX963798">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963798</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13029613, constructed from sample accession ERS629065 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_2).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS629065" refname="GPS_PL_9264_11-sc-2191176" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS629065</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_PL_9264_11-sc-2191176</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13029613</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#28" center_name="The Wellcome Trust Sanger Institute" accession="ERX963994">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963994</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_4#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 13032784, constructed from sample accession ERS634665 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634665" refname="GPS_TH_BK_0541-sc-2191367" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634665</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0541-sc-2191367</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032784</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#29" center_name="The Wellcome Trust Sanger Institute" accession="ERX963995">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963995</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032806, constructed from sample accession ERS634668 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634668" refname="GPS_TH_BK_0542-sc-2191370" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634668</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0542-sc-2191370</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032806</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#30" center_name="The Wellcome Trust Sanger Institute" accession="ERX963996">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963996</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032827, constructed from sample accession ERS634672 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634672" refname="GPS_TH_BK_0546-sc-2191374" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634672</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0546-sc-2191374</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032827</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX963997">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963997</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_4#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 13032849, constructed from sample accession ERS634680 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634680" refname="GPS_TH_BK_0547-sc-2191382" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634680</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0547-sc-2191382</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032849</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX963998">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963998</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032879, constructed from sample accession ERS634683 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634683" refname="GPS_TH_BK_0548-sc-2191385" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634683</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0548-sc-2191385</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032879</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX963999">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX963999</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032749, constructed from sample accession ERS634686 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634686" refname="GPS_TH_BK_0549-sc-2191388" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634686</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0549-sc-2191388</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032749</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX964000">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964000</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032761, constructed from sample accession ERS634689 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634689" refname="GPS_TH_BK_0551-sc-2191391" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634689</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0551-sc-2191391</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032761</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX964001">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964001</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032773, constructed from sample accession ERS634693 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634693" refname="GPS_TH_BK_0553-sc-2191395" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634693</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0553-sc-2191395</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032773</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX964002">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964002</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032786, constructed from sample accession ERS634695 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634695" refname="GPS_TH_BK_0554-sc-2191398" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634695</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0554-sc-2191398</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032786</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX964003">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964003</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032807, constructed from sample accession ERS634696 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634696" refname="GPS_TH_BK_0555-sc-2191400" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634696</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0555-sc-2191400</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032807</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX964004">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964004</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032829, constructed from sample accession ERS634697 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634697" refname="GPS_TH_BK_0557-sc-2191401" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634697</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0557-sc-2191401</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032829</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#39" center_name="The Wellcome Trust Sanger Institute" accession="ERX964005">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964005</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#39</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032851, constructed from sample accession ERS634698 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634698" refname="GPS_TH_BK_0561-sc-2191402" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634698</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0561-sc-2191402</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032851</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_4#40" center_name="The Wellcome Trust Sanger Institute" accession="ERX964006">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964006</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_4#40</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_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 13032881, constructed from sample accession ERS634699 for study accession ERP001505.  This is part of an Illumina multiplexed sequencing run (15682_4).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS634699" refname="GPS_TH_BK_0562-sc-2191403" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS634699</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">GPS_TH_BK_0562-sc-2191403</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13032881</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="68"/>
        </LIBRARY_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>
