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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="SC_EXP_12054_5#17" center_name="The Wellcome Trust Sanger Institute" accession="ERX450623">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450623</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232116, constructed from sample accession ERS209369 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209369" refname="2240237a-sc-2013-01-29T12:42:05Z-1553450" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209369</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904509</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240237a-sc-2013-01-29T12:42:05Z-1553450</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232116</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#18" center_name="The Wellcome Trust Sanger Institute" accession="ERX450624">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450624</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232128, constructed from sample accession ERS209370 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209370" refname="2240238a-sc-2013-01-29T12:42:06Z-1553451" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209370</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904512</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240238a-sc-2013-01-29T12:42:06Z-1553451</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232128</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#19" center_name="The Wellcome Trust Sanger Institute" accession="ERX450625">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450625</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232140, constructed from sample accession ERS209371 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209371" refname="2240239a-sc-2013-01-29T12:42:07Z-1553452" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209371</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904515</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240239a-sc-2013-01-29T12:42:07Z-1553452</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232140</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#20" center_name="The Wellcome Trust Sanger Institute" accession="ERX450626">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450626</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232152, constructed from sample accession ERS209372 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209372" refname="2240240a-sc-2013-01-29T12:42:08Z-1553453" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209372</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904511</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240240a-sc-2013-01-29T12:42:08Z-1553453</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232152</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#21" center_name="The Wellcome Trust Sanger Institute" accession="ERX450627">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450627</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232164, constructed from sample accession ERS209373 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209373" refname="2240241a-sc-2013-01-29T12:42:09Z-1553454" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209373</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904516</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240241a-sc-2013-01-29T12:42:09Z-1553454</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232164</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#22" center_name="The Wellcome Trust Sanger Institute" accession="ERX450628">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450628</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232176, constructed from sample accession ERS209374 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209374" refname="2240242a-sc-2013-01-29T12:42:10Z-1553455" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209374</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904514</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240242a-sc-2013-01-29T12:42:10Z-1553455</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232176</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#23" center_name="The Wellcome Trust Sanger Institute" accession="ERX450629">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450629</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232188, constructed from sample accession ERS209375 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209375" refname="2240243a-sc-2013-01-29T12:42:11Z-1553456" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209375</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904517</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240243a-sc-2013-01-29T12:42:11Z-1553456</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232188</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#24" center_name="The Wellcome Trust Sanger Institute" accession="ERX450630">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450630</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232200, constructed from sample accession ERS209376 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209376" refname="2240245a-sc-2013-01-29T12:42:12Z-1553457" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209376</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904518</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240245a-sc-2013-01-29T12:42:12Z-1553457</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232200</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#25" center_name="The Wellcome Trust Sanger Institute" accession="ERX450631">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450631</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232117, constructed from sample accession ERS209377 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209377" refname="2240248a-sc-2013-01-29T12:42:13Z-1553458" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209377</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904520</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240248a-sc-2013-01-29T12:42:13Z-1553458</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232117</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#26" center_name="The Wellcome Trust Sanger Institute" accession="ERX450632">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450632</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232129, constructed from sample accession ERS209378 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209378" refname="2240249b-sc-2013-01-29T12:42:14Z-1553459" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209378</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904522</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240249b-sc-2013-01-29T12:42:14Z-1553459</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232129</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#27" center_name="The Wellcome Trust Sanger Institute" accession="ERX450633">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450633</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232141, constructed from sample accession ERS209379 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209379" refname="2240250a-sc-2013-01-29T12:42:15Z-1553460" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209379</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904521</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240250a-sc-2013-01-29T12:42:15Z-1553460</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232141</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#28" center_name="The Wellcome Trust Sanger Institute" accession="ERX450634">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450634</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232153, constructed from sample accession ERS209380 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209380" refname="2240251a-sc-2013-01-29T12:42:16Z-1553461" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209380</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904519</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240251a-sc-2013-01-29T12:42:16Z-1553461</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232153</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#29" center_name="The Wellcome Trust Sanger Institute" accession="ERX450635">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450635</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232165, constructed from sample accession ERS209381 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209381" refname="2240252a-sc-2013-01-29T12:42:16Z-1553462" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209381</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904524</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240252a-sc-2013-01-29T12:42:16Z-1553462</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232165</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#30" center_name="The Wellcome Trust Sanger Institute" accession="ERX450636">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450636</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232177, constructed from sample accession ERS209382 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209382" refname="2240253a-sc-2013-01-29T12:42:17Z-1553463" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209382</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904523</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240253a-sc-2013-01-29T12:42:17Z-1553463</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232177</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX450637">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450637</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232189, constructed from sample accession ERS209383 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209383" refname="2240254a-sc-2013-01-29T12:42:18Z-1553464" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209383</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904527</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240254a-sc-2013-01-29T12:42:18Z-1553464</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232189</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX450638">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450638</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232201, constructed from sample accession ERS209384 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209384" refname="2240255a-sc-2013-01-29T12:42:19Z-1553465" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209384</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904526</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240255a-sc-2013-01-29T12:42:19Z-1553465</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232201</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX450639">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450639</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232118, constructed from sample accession ERS209385 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209385" refname="2240256a-sc-2013-01-29T12:42:20Z-1553466" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209385</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904525</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240256a-sc-2013-01-29T12:42:20Z-1553466</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232118</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX450640">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450640</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232130, constructed from sample accession ERS209386 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209386" refname="2240257a-sc-2013-01-29T12:42:21Z-1553467" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209386</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904529</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240257a-sc-2013-01-29T12:42:21Z-1553467</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232130</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX450641">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450641</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232142, constructed from sample accession ERS209387 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209387" refname="2240259a-sc-2013-01-29T12:42:22Z-1553468" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209387</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904528</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240259a-sc-2013-01-29T12:42:22Z-1553468</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232142</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX450642">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450642</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232154, constructed from sample accession ERS209388 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209388" refname="2240261a-sc-2013-01-29T12:42:23Z-1553469" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209388</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904531</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240261a-sc-2013-01-29T12:42:23Z-1553469</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232154</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX450643">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450643</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232166, constructed from sample accession ERS209389 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209389" refname="2240263a-sc-2013-01-29T12:42:24Z-1553470" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209389</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904530</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240263a-sc-2013-01-29T12:42:24Z-1553470</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232166</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX450644">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450644</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232178, constructed from sample accession ERS209390 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209390" refname="2240264a-sc-2013-01-29T12:42:25Z-1553471" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209390</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904532</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240264a-sc-2013-01-29T12:42:25Z-1553471</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232178</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#39" center_name="The Wellcome Trust Sanger Institute" accession="ERX450645">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450645</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#39</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232190, constructed from sample accession ERS209391 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209391" refname="2240267a-sc-2013-01-29T12:42:26Z-1553472" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209391</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904533</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240267a-sc-2013-01-29T12:42:26Z-1553472</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232190</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#40" center_name="The Wellcome Trust Sanger Institute" accession="ERX450646">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450646</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#40</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232202, constructed from sample accession ERS209392 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209392" refname="2240272a-sc-2013-01-29T12:42:27Z-1553473" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209392</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904534</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240272a-sc-2013-01-29T12:42:27Z-1553473</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232202</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#41" center_name="The Wellcome Trust Sanger Institute" accession="ERX450647">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450647</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#41</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232119, constructed from sample accession ERS209393 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209393" refname="2240273a-sc-2013-01-29T12:42:28Z-1553474" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209393</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904535</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240273a-sc-2013-01-29T12:42:28Z-1553474</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232119</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#42" center_name="The Wellcome Trust Sanger Institute" accession="ERX450648">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450648</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#42</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232131, constructed from sample accession ERS209394 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209394" refname="2240274a-sc-2013-01-29T12:42:29Z-1553475" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209394</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904538</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240274a-sc-2013-01-29T12:42:29Z-1553475</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232131</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#43" center_name="The Wellcome Trust Sanger Institute" accession="ERX450649">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450649</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#43</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232143, constructed from sample accession ERS209395 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209395" refname="2240277a-sc-2013-01-29T12:42:30Z-1553476" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209395</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904536</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240277a-sc-2013-01-29T12:42:30Z-1553476</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232143</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#44" center_name="The Wellcome Trust Sanger Institute" accession="ERX450650">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450650</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#44</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232155, constructed from sample accession ERS209396 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209396" refname="2240284a-sc-2013-01-29T12:42:31Z-1553477" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209396</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904537</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240284a-sc-2013-01-29T12:42:31Z-1553477</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232155</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#45" center_name="The Wellcome Trust Sanger Institute" accession="ERX450651">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450651</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#45</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232167, constructed from sample accession ERS209397 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209397" refname="2240287a-sc-2013-01-29T12:42:32Z-1553478" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209397</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904541</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240287a-sc-2013-01-29T12:42:32Z-1553478</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232167</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#46" center_name="The Wellcome Trust Sanger Institute" accession="ERX450652">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450652</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#46</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232179, constructed from sample accession ERS209398 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209398" refname="2240288a-sc-2013-01-29T12:42:33Z-1553479" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209398</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904539</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240288a-sc-2013-01-29T12:42:33Z-1553479</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232179</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#47" center_name="The Wellcome Trust Sanger Institute" accession="ERX450653">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450653</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#47</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232191, constructed from sample accession ERS209399 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209399" refname="2240289a-sc-2013-01-29T12:42:34Z-1553480" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209399</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904540</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240289a-sc-2013-01-29T12:42:34Z-1553480</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232191</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#48" center_name="The Wellcome Trust Sanger Institute" accession="ERX450654">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450654</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#48</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232203, constructed from sample accession ERS209400 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209400" refname="2240290a-sc-2013-01-29T12:42:35Z-1553482" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209400</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904543</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240290a-sc-2013-01-29T12:42:35Z-1553482</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232203</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#49" center_name="The Wellcome Trust Sanger Institute" accession="ERX450655">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450655</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#49</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232120, constructed from sample accession ERS209401 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209401" refname="2240291a-sc-2013-01-29T12:42:36Z-1553483" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209401</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904542</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240291a-sc-2013-01-29T12:42:36Z-1553483</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232120</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#50" center_name="The Wellcome Trust Sanger Institute" accession="ERX450656">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450656</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#50</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232132, constructed from sample accession ERS209402 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209402" refname="2240293a-sc-2013-01-29T12:42:37Z-1553484" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209402</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904545</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240293a-sc-2013-01-29T12:42:37Z-1553484</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232132</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#51" center_name="The Wellcome Trust Sanger Institute" accession="ERX450657">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450657</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#51</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232144, constructed from sample accession ERS209403 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209403" refname="2240294a-sc-2013-01-29T12:42:38Z-1553485" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209403</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904547</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240294a-sc-2013-01-29T12:42:38Z-1553485</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232144</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#52" center_name="The Wellcome Trust Sanger Institute" accession="ERX450658">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450658</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#52</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232156, constructed from sample accession ERS209404 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209404" refname="2240296a-sc-2013-01-29T12:42:39Z-1553486" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209404</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904544</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240296a-sc-2013-01-29T12:42:39Z-1553486</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232156</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#53" center_name="The Wellcome Trust Sanger Institute" accession="ERX450659">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450659</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#53</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232168, constructed from sample accession ERS209405 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209405" refname="2240299a-sc-2013-01-29T12:42:40Z-1553487" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209405</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904546</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240299a-sc-2013-01-29T12:42:40Z-1553487</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232168</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#54" center_name="The Wellcome Trust Sanger Institute" accession="ERX450660">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450660</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#54</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232180, constructed from sample accession ERS209406 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209406" refname="2240300a-sc-2013-01-29T12:42:41Z-1553488" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209406</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904548</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240300a-sc-2013-01-29T12:42:41Z-1553488</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232180</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#55" center_name="The Wellcome Trust Sanger Institute" accession="ERX450661">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450661</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#55</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232192, constructed from sample accession ERS209407 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209407" refname="2240301a-sc-2013-01-29T12:42:42Z-1553489" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209407</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904553</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240301a-sc-2013-01-29T12:42:42Z-1553489</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232192</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#56" center_name="The Wellcome Trust Sanger Institute" accession="ERX450662">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450662</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#56</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232204, constructed from sample accession ERS209408 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209408" refname="2240302a-sc-2013-01-29T12:42:43Z-1553490" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209408</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904555</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240302a-sc-2013-01-29T12:42:43Z-1553490</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232204</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#57" center_name="The Wellcome Trust Sanger Institute" accession="ERX450663">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450663</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#57</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232121, constructed from sample accession ERS209409 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209409" refname="2240303a-sc-2013-01-29T12:42:44Z-1553491" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209409</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904552</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240303a-sc-2013-01-29T12:42:44Z-1553491</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232121</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#58" center_name="The Wellcome Trust Sanger Institute" accession="ERX450664">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450664</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#58</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232133, constructed from sample accession ERS209410 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209410" refname="2240305a-sc-2013-01-29T12:42:45Z-1553492" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209410</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904554</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240305a-sc-2013-01-29T12:42:45Z-1553492</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232133</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#59" center_name="The Wellcome Trust Sanger Institute" accession="ERX450665">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450665</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#59</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232145, constructed from sample accession ERS209411 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209411" refname="2240306a-sc-2013-01-29T12:42:46Z-1553493" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209411</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904549</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240306a-sc-2013-01-29T12:42:46Z-1553493</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232145</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#60" center_name="The Wellcome Trust Sanger Institute" accession="ERX450666">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450666</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#60</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#60</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232157, constructed from sample accession ERS209412 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209412" refname="2240307a-sc-2013-01-29T12:42:47Z-1553494" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209412</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904550</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240307a-sc-2013-01-29T12:42:47Z-1553494</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232157</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#61" center_name="The Wellcome Trust Sanger Institute" accession="ERX450667">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450667</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#61</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232169, constructed from sample accession ERS209413 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209413" refname="2240308a-sc-2013-01-29T12:42:48Z-1553495" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209413</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904551</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240308a-sc-2013-01-29T12:42:48Z-1553495</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232169</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#62" center_name="The Wellcome Trust Sanger Institute" accession="ERX450668">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450668</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#62</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232181, constructed from sample accession ERS209414 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209414" refname="2240309a-sc-2013-01-29T12:42:49Z-1553496" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209414</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904556</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240309a-sc-2013-01-29T12:42:49Z-1553496</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232181</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#63" center_name="The Wellcome Trust Sanger Institute" accession="ERX450669">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450669</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#63</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#63</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232193, constructed from sample accession ERS209415 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209415" refname="2240310a-sc-2013-01-29T12:42:49Z-1553497" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209415</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904563</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240310a-sc-2013-01-29T12:42:49Z-1553497</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232193</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#64" center_name="The Wellcome Trust Sanger Institute" accession="ERX450670">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450670</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#64</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#64</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232205, constructed from sample accession ERS209416 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209416" refname="2240314a-sc-2013-01-29T12:42:50Z-1553498" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209416</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904559</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240314a-sc-2013-01-29T12:42:50Z-1553498</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232205</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#65" center_name="The Wellcome Trust Sanger Institute" accession="ERX450671">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450671</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#65</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#65</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232122, constructed from sample accession ERS209417 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209417" refname="2240315a-sc-2013-01-29T12:42:51Z-1553499" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209417</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904557</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240315a-sc-2013-01-29T12:42:51Z-1553499</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232122</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#66" center_name="The Wellcome Trust Sanger Institute" accession="ERX450672">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450672</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#66</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#66</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232134, constructed from sample accession ERS209418 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209418" refname="2240317a-sc-2013-01-29T12:42:52Z-1553500" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209418</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904560</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240317a-sc-2013-01-29T12:42:52Z-1553500</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232134</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#67" center_name="The Wellcome Trust Sanger Institute" accession="ERX450673">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450673</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#67</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232146, constructed from sample accession ERS209419 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209419" refname="2240318a-sc-2013-01-29T12:42:53Z-1553501" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209419</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904562</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240318a-sc-2013-01-29T12:42:53Z-1553501</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232146</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#68" center_name="The Wellcome Trust Sanger Institute" accession="ERX450674">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450674</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#68</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232158, constructed from sample accession ERS209420 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209420" refname="2240319a-sc-2013-01-29T12:42:54Z-1553502" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209420</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904561</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240319a-sc-2013-01-29T12:42:54Z-1553502</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232158</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#69" center_name="The Wellcome Trust Sanger Institute" accession="ERX450675">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450675</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#69</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#69</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232170, constructed from sample accession ERS209421 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209421" refname="2240320a-sc-2013-01-29T12:42:55Z-1553503" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209421</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904558</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240320a-sc-2013-01-29T12:42:55Z-1553503</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232170</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#70" center_name="The Wellcome Trust Sanger Institute" accession="ERX450676">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450676</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#70</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#70</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232182, constructed from sample accession ERS209422 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209422" refname="2240321a-sc-2013-01-29T12:42:56Z-1553504" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209422</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904564</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240321a-sc-2013-01-29T12:42:56Z-1553504</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232182</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#71" center_name="The Wellcome Trust Sanger Institute" accession="ERX450677">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450677</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#71</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#71</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232194, constructed from sample accession ERS209423 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence GTGTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209423" refname="2240322a-sc-2013-01-29T12:42:57Z-1553505" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209423</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904565</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240322a-sc-2013-01-29T12:42:57Z-1553505</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232194</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#72" center_name="The Wellcome Trust Sanger Institute" accession="ERX450678">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450678</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#72</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#72</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232206, constructed from sample accession ERS209424 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence GACGGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209424" refname="2240323a-sc-2013-01-29T12:42:58Z-1553506" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209424</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904566</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240323a-sc-2013-01-29T12:42:58Z-1553506</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232206</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#73" center_name="The Wellcome Trust Sanger Institute" accession="ERX450679">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450679</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#73</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#73</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232123, constructed from sample accession ERS209425 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209425" refname="2240324a-sc-2013-01-29T12:42:59Z-1553507" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209425</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904567</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240324a-sc-2013-01-29T12:42:59Z-1553507</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232123</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#74" center_name="The Wellcome Trust Sanger Institute" accession="ERX450680">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450680</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#74</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232135, constructed from sample accession ERS209426 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209426" refname="2240325a-sc-2013-01-29T12:43:00Z-1553508" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209426</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904568</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240325a-sc-2013-01-29T12:43:00Z-1553508</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232135</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#75" center_name="The Wellcome Trust Sanger Institute" accession="ERX450681">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450681</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#75</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232147, constructed from sample accession ERS209427 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence GAATCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209427" refname="2240326a-sc-2013-01-29T12:43:01Z-1553509" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209427</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904569</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240326a-sc-2013-01-29T12:43:01Z-1553509</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232147</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#76" center_name="The Wellcome Trust Sanger Institute" accession="ERX450682">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450682</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#76</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232159, constructed from sample accession ERS209428 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209428" refname="2240328a-sc-2013-01-29T12:43:02Z-1553510" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209428</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904571</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240328a-sc-2013-01-29T12:43:02Z-1553510</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232159</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#77" center_name="The Wellcome Trust Sanger Institute" accession="ERX450683">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450683</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#77</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232171, constructed from sample accession ERS209429 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209429" refname="2240329a-sc-2013-01-29T12:43:03Z-1553511" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209429</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904570</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240329a-sc-2013-01-29T12:43:03Z-1553511</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232171</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#78" center_name="The Wellcome Trust Sanger Institute" accession="ERX450684">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450684</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#78</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#78</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232183, constructed from sample accession ERS209430 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209430" refname="2240330a-sc-2013-01-29T12:43:03Z-1553512" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209430</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904572</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240330a-sc-2013-01-29T12:43:03Z-1553512</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232183</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#79" center_name="The Wellcome Trust Sanger Institute" accession="ERX450685">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450685</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#79</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232195, constructed from sample accession ERS209431 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209431" refname="2240332a-sc-2013-01-29T12:43:04Z-1553513" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209431</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904573</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240332a-sc-2013-01-29T12:43:04Z-1553513</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232195</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#80" center_name="The Wellcome Trust Sanger Institute" accession="ERX450686">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450686</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#80</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232207, constructed from sample accession ERS209432 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence GTCGCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209432" refname="2240333a-sc-2013-01-29T12:43:05Z-1553514" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209432</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904574</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240333a-sc-2013-01-29T12:43:05Z-1553514</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232207</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#81" center_name="The Wellcome Trust Sanger Institute" accession="ERX450687">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450687</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#81</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232124, constructed from sample accession ERS209433 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209433" refname="2240334a-sc-2013-01-29T12:43:06Z-1553515" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209433</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904575</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240334a-sc-2013-01-29T12:43:06Z-1553515</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232124</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#82" center_name="The Wellcome Trust Sanger Institute" accession="ERX450688">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450688</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#82</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#82</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232136, constructed from sample accession ERS209434 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209434" refname="2240335a-sc-2013-01-29T12:43:07Z-1553516" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209434</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904576</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240335a-sc-2013-01-29T12:43:07Z-1553516</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232136</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#83" center_name="The Wellcome Trust Sanger Institute" accession="ERX450689">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450689</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#83</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#83</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232148, constructed from sample accession ERS209435 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence GCTCCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209435" refname="2240641a-sc-2013-01-29T12:43:08Z-1553517" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209435</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904577</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240641a-sc-2013-01-29T12:43:08Z-1553517</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232148</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_4#7" center_name="The Wellcome Trust Sanger Institute" accession="ERX450586">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450586</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_4#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_4#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232283, constructed from sample accession ERS209276 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_4).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209276" refname="2240086a-sc-2013-01-29T12:40:35Z-1553356" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209276</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2049634</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240086a-sc-2013-01-29T12:40:35Z-1553356</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232283</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="234" 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_12054_4#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX450587">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450587</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_4#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_4#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232295, constructed from sample accession ERS209277 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_4).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209277" refname="2240088a-sc-2013-01-29T12:40:36Z-1553357" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209277</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2047676</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240088a-sc-2013-01-29T12:40:36Z-1553357</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232295</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="234" 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_12054_4#9" center_name="The Wellcome Trust Sanger Institute" accession="ERX450588">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450588</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_4#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_4#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232212, constructed from sample accession ERS209278 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_4).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209278" refname="2240090a-sc-2013-01-29T12:40:37Z-1553358" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209278</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2048032</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240090a-sc-2013-01-29T12:40:37Z-1553358</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232212</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="234" 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_12054_4#66" center_name="The Wellcome Trust Sanger Institute" accession="ERX450589">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450589</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_4#66</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_4#66</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232231, constructed from sample accession ERS209335 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_4).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209335" refname="2240181a-sc-2013-01-29T12:41:33Z-1553416" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209335</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2048192</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240181a-sc-2013-01-29T12:41:33Z-1553416</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232231</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="234" 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_12054_4#67" center_name="The Wellcome Trust Sanger Institute" accession="ERX450590">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450590</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_4#67</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_4#67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232243, constructed from sample accession ERS209336 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_4).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209336" refname="2240184b-sc-2013-01-29T12:41:34Z-1553417" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209336</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2049733</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240184b-sc-2013-01-29T12:41:34Z-1553417</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232243</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="234" 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_12054_4#68" center_name="The Wellcome Trust Sanger Institute" accession="ERX450591">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450591</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_4#68</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_4#68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232255, constructed from sample accession ERS209337 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_4).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209337" refname="2240186a-sc-2013-01-29T12:41:35Z-1553418" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209337</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2047836</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240186a-sc-2013-01-29T12:41:35Z-1553418</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232255</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="234" 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_12054_4#69" center_name="The Wellcome Trust Sanger Institute" accession="ERX450592">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450592</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_4#69</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_4#69</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232267, constructed from sample accession ERS209338 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_4).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209338" refname="2240187a-sc-2013-01-29T12:41:36Z-1553419" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209338</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2048193</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240187a-sc-2013-01-29T12:41:36Z-1553419</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232267</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="234" 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_12054_4#70" center_name="The Wellcome Trust Sanger Institute" accession="ERX450593">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450593</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_4#70</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_4#70</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232279, constructed from sample accession ERS209339 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_4).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209339" refname="2240188a-sc-2013-01-29T12:41:37Z-1553420" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209339</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2049734</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240188a-sc-2013-01-29T12:41:37Z-1553420</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232279</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="234" 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_12054_4#71" center_name="The Wellcome Trust Sanger Institute" accession="ERX450594">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450594</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_4#71</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_4#71</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232291, constructed from sample accession ERS209340 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_4).  This submission includes reads tagged with the sequence GTGTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209340" refname="2240191a-sc-2013-01-29T12:41:38Z-1553421" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209340</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2047837</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240191a-sc-2013-01-29T12:41:38Z-1553421</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232291</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="234" 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_12054_4#72" center_name="The Wellcome Trust Sanger Institute" accession="ERX450595">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450595</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_4#72</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_4#72</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232303, constructed from sample accession ERS209341 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_4).  This submission includes reads tagged with the sequence GACGGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209341" refname="2240194a-sc-2013-01-29T12:41:39Z-1553422" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209341</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2048194</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240194a-sc-2013-01-29T12:41:39Z-1553422</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232303</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="234" 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_12054_4#73" center_name="The Wellcome Trust Sanger Institute" accession="ERX450596">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450596</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_4#73</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_4#73</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232220, constructed from sample accession ERS209342 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_4).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209342" refname="2240197a-sc-2013-01-29T12:41:39Z-1553423" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209342</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2049735</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240197a-sc-2013-01-29T12:41:39Z-1553423</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232220</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="234" 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_12054_4#74" center_name="The Wellcome Trust Sanger Institute" accession="ERX450597">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450597</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_4#74</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_4#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232232, constructed from sample accession ERS209343 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_4).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209343" refname="2240200a-sc-2013-01-29T12:41:40Z-1553424" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209343</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2047838</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240200a-sc-2013-01-29T12:41:40Z-1553424</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232232</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="234" 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_12054_4#75" center_name="The Wellcome Trust Sanger Institute" accession="ERX450598">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450598</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_4#75</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_4#75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232244, constructed from sample accession ERS209344 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_4).  This submission includes reads tagged with the sequence GAATCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209344" refname="2240201a-sc-2013-01-29T12:41:41Z-1553425" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209344</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2048195</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240201a-sc-2013-01-29T12:41:41Z-1553425</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232244</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="234" 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_12054_4#76" center_name="The Wellcome Trust Sanger Institute" accession="ERX450599">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450599</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_4#76</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_4#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232256, constructed from sample accession ERS209345 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_4).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209345" refname="2240202a-sc-2013-01-29T12:41:42Z-1553426" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209345</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2049736</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240202a-sc-2013-01-29T12:41:42Z-1553426</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232256</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="234" 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_12054_4#77" center_name="The Wellcome Trust Sanger Institute" accession="ERX450600">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450600</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_4#77</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_4#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232268, constructed from sample accession ERS209346 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_4).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209346" refname="2240203a-sc-2013-01-29T12:41:43Z-1553427" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209346</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2047839</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240203a-sc-2013-01-29T12:41:43Z-1553427</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232268</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="234" 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_12054_4#78" center_name="The Wellcome Trust Sanger Institute" accession="ERX450601">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450601</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_4#78</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_4#78</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232280, constructed from sample accession ERS209347 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_4).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209347" refname="2240205a-sc-2013-01-29T12:41:44Z-1553428" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2048196</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240205a-sc-2013-01-29T12:41:44Z-1553428</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232280</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="234" 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_12054_4#79" center_name="The Wellcome Trust Sanger Institute" accession="ERX450602">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450602</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_4#79</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_4#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232292, constructed from sample accession ERS209348 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_4).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209348" refname="2240206a-sc-2013-01-29T12:41:45Z-1553429" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2049737</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240206a-sc-2013-01-29T12:41:45Z-1553429</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232292</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="234" 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_12054_4#80" center_name="The Wellcome Trust Sanger Institute" accession="ERX450603">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450603</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_4#80</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_4#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232304, constructed from sample accession ERS209349 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_4).  This submission includes reads tagged with the sequence GTCGCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209349" refname="2240207b-sc-2013-01-29T12:41:46Z-1553430" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209349</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2047840</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240207b-sc-2013-01-29T12:41:46Z-1553430</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232304</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="234" 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_12054_4#81" center_name="The Wellcome Trust Sanger Institute" accession="ERX450604">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450604</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_4#81</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_4#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232221, constructed from sample accession ERS209350 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_4).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209350" refname="2240208b-sc-2013-01-29T12:41:47Z-1553431" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209350</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2048197</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240208b-sc-2013-01-29T12:41:47Z-1553431</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232221</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="234" 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_12054_4#82" center_name="The Wellcome Trust Sanger Institute" accession="ERX450605">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450605</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_4#82</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_4#82</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232233, constructed from sample accession ERS209351 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_4).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209351" refname="2240211a-sc-2013-01-29T12:41:48Z-1553432" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1965336</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240211a-sc-2013-01-29T12:41:48Z-1553432</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232233</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="234" 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_12054_4#83" center_name="The Wellcome Trust Sanger Institute" accession="ERX450606">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450606</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_4#83</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_4#83</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232245, constructed from sample accession ERS209352 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_4).  This submission includes reads tagged with the sequence GCTCCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209352" refname="2240213a-sc-2013-01-29T12:41:49Z-1553433" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2047841</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240213a-sc-2013-01-29T12:41:49Z-1553433</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232245</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="234" 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_12054_5#1" center_name="The Wellcome Trust Sanger Institute" accession="ERX450607">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450607</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232114, constructed from sample accession ERS209353 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209353" refname="2240214a-sc-2013-01-29T12:41:50Z-1553434" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209353</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904494</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240214a-sc-2013-01-29T12:41:50Z-1553434</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232114</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#2" center_name="The Wellcome Trust Sanger Institute" accession="ERX450608">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450608</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232126, constructed from sample accession ERS209354 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209354" refname="2240215a-sc-2013-01-29T12:41:51Z-1553435" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209354</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904496</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240215a-sc-2013-01-29T12:41:51Z-1553435</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232126</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#3" center_name="The Wellcome Trust Sanger Institute" accession="ERX450609">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450609</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232138, constructed from sample accession ERS209355 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209355" refname="2240216b-sc-2013-01-29T12:41:52Z-1553436" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209355</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904497</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240216b-sc-2013-01-29T12:41:52Z-1553436</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232138</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#4" center_name="The Wellcome Trust Sanger Institute" accession="ERX450610">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450610</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232150, constructed from sample accession ERS209356 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209356" refname="2240219a-sc-2013-01-29T12:41:53Z-1553437" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209356</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904501</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240219a-sc-2013-01-29T12:41:53Z-1553437</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232150</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#5" center_name="The Wellcome Trust Sanger Institute" accession="ERX450611">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450611</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232162, constructed from sample accession ERS209357 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209357" refname="2240220a-sc-2013-01-29T12:41:54Z-1553438" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209357</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904498</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240220a-sc-2013-01-29T12:41:54Z-1553438</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232162</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#6" center_name="The Wellcome Trust Sanger Institute" accession="ERX450612">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450612</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232174, constructed from sample accession ERS209358 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209358" refname="2240222a-sc-2013-01-29T12:41:55Z-1553439" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209358</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904499</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240222a-sc-2013-01-29T12:41:55Z-1553439</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232174</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#7" center_name="The Wellcome Trust Sanger Institute" accession="ERX450613">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450613</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232186, constructed from sample accession ERS209359 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209359" refname="2240223a-sc-2013-01-29T12:41:56Z-1553440" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209359</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904500</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240223a-sc-2013-01-29T12:41:56Z-1553440</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232186</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX450614">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450614</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232198, constructed from sample accession ERS209360 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209360" refname="2240224a-sc-2013-01-29T12:41:57Z-1553441" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209360</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904502</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240224a-sc-2013-01-29T12:41:57Z-1553441</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232198</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#9" center_name="The Wellcome Trust Sanger Institute" accession="ERX450615">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450615</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232115, constructed from sample accession ERS209361 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209361" refname="2240225a-sc-2013-01-29T12:41:58Z-1553442" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209361</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904503</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240225a-sc-2013-01-29T12:41:58Z-1553442</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232115</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#10" center_name="The Wellcome Trust Sanger Institute" accession="ERX450616">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450616</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232127, constructed from sample accession ERS209362 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209362" refname="2240226a-sc-2013-01-29T12:41:59Z-1553443" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209362</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904506</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240226a-sc-2013-01-29T12:41:59Z-1553443</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232127</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#11" center_name="The Wellcome Trust Sanger Institute" accession="ERX450617">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450617</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232139, constructed from sample accession ERS209363 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209363" refname="2240227a-sc-2013-01-29T12:42:00Z-1553444" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209363</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904504</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240227a-sc-2013-01-29T12:42:00Z-1553444</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232139</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#12" center_name="The Wellcome Trust Sanger Institute" accession="ERX450618">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450618</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232151, constructed from sample accession ERS209364 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209364" refname="2240228a-sc-2013-01-29T12:42:01Z-1553445" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209364</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904505</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240228a-sc-2013-01-29T12:42:01Z-1553445</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232151</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#13" center_name="The Wellcome Trust Sanger Institute" accession="ERX450619">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450619</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232163, constructed from sample accession ERS209365 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209365" refname="2240229a-sc-2013-01-29T12:42:01Z-1553446" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209365</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904508</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240229a-sc-2013-01-29T12:42:01Z-1553446</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232163</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#14" center_name="The Wellcome Trust Sanger Institute" accession="ERX450620">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450620</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232175, constructed from sample accession ERS209366 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209366" refname="2240230a-sc-2013-01-29T12:42:02Z-1553447" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209366</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904507</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240230a-sc-2013-01-29T12:42:02Z-1553447</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232175</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#15" center_name="The Wellcome Trust Sanger Institute" accession="ERX450621">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450621</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232187, constructed from sample accession ERS209367 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209367" refname="2240231a-sc-2013-01-29T12:42:03Z-1553448" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209367</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904510</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240231a-sc-2013-01-29T12:42:03Z-1553448</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232187</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_12054_5#16" center_name="The Wellcome Trust Sanger Institute" accession="ERX450622">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX450622</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_12054_5#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_12054_5#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000951" refname="Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000951</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Neisseria_meningitidis_study-sc-2011-10-17T10:18:46Z-1995</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 9232199, constructed from sample accession ERS209368 for study accession ERP000951.  This is part of an Illumina multiplexed sequencing run (12054_5).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS209368" refname="2240232a-sc-2013-01-29T12:42:04Z-1553449" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS209368</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA1904513</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">2240232a-sc-2013-01-29T12:42:04Z-1553449</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9232199</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230" NOMINAL_SDEV="71"/>
        </LIBRARY_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>
