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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="SC_EXP_15682_6#68" center_name="The Wellcome Trust Sanger Institute" accession="ERX964236">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964236</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#68</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053264, constructed from sample accession ERS633494 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633494" refname="UOS_IPD_167-sc-2201325" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633494</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_167-sc-2201325</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053264</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#69" center_name="The Wellcome Trust Sanger Institute" accession="ERX964237">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964237</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#69</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#69</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053276, constructed from sample accession ERS633495 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633495" refname="UOS_IPD_168-sc-2201326" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633495</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_168-sc-2201326</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053276</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#70" center_name="The Wellcome Trust Sanger Institute" accession="ERX964238">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964238</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#70</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#70</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053288, constructed from sample accession ERS633496 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633496" refname="UOS_IPD_169-sc-2201327" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633496</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_169-sc-2201327</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053288</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#71" center_name="The Wellcome Trust Sanger Institute" accession="ERX964239">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964239</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#71</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#71</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053300, constructed from sample accession ERS633497 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence GTGTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633497" refname="UOS_IPD_176-sc-2201328" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633497</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_176-sc-2201328</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053300</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#72" center_name="The Wellcome Trust Sanger Institute" accession="ERX964240">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964240</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#72</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#72</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053312, constructed from sample accession ERS633498 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence GACGGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633498" refname="UOS_IPD_177-sc-2201329" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633498</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_177-sc-2201329</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053312</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#73" center_name="The Wellcome Trust Sanger Institute" accession="ERX964241">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964241</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#73</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#73</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053229, constructed from sample accession ERS633499 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633499" refname="UOS_IPD_178-sc-2201330" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633499</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_178-sc-2201330</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053229</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#74" center_name="The Wellcome Trust Sanger Institute" accession="ERX964242">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964242</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#74</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053241, constructed from sample accession ERS633500 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633500" refname="UOS_IPD_179-sc-2201331" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633500</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_179-sc-2201331</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053241</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#75" center_name="The Wellcome Trust Sanger Institute" accession="ERX964243">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964243</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#75</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053253, constructed from sample accession ERS633501 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence GAATCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633501" refname="UOS_IPD_182-sc-2201332" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633501</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_182-sc-2201332</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053253</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#76" center_name="The Wellcome Trust Sanger Institute" accession="ERX964244">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964244</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#76</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053265, constructed from sample accession ERS633502 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633502" refname="UOS_IPD_183-sc-2201333" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633502</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_183-sc-2201333</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053265</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#77" center_name="The Wellcome Trust Sanger Institute" accession="ERX964245">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964245</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#77</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053277, constructed from sample accession ERS633503 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633503" refname="UOS_IPD_184-sc-2201334" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633503</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_184-sc-2201334</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053277</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#78" center_name="The Wellcome Trust Sanger Institute" accession="ERX964246">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964246</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#78</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#78</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053289, constructed from sample accession ERS633504 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633504" refname="UOS_IPD_185-sc-2201335" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633504</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_185-sc-2201335</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053289</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#79" center_name="The Wellcome Trust Sanger Institute" accession="ERX964247">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964247</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#79</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053301, constructed from sample accession ERS633505 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633505" refname="UOS_IPD_186-sc-2201336" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633505</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_186-sc-2201336</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053301</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#80" center_name="The Wellcome Trust Sanger Institute" accession="ERX964248">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964248</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#80</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053313, constructed from sample accession ERS633506 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence GTCGCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633506" refname="UOS_IPD_187-sc-2201337" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633506</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_187-sc-2201337</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053313</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#81" center_name="The Wellcome Trust Sanger Institute" accession="ERX964249">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964249</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#81</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053230, constructed from sample accession ERS633507 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633507" refname="UOS_IPD_188-sc-2201338" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633507</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_188-sc-2201338</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053230</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#82" center_name="The Wellcome Trust Sanger Institute" accession="ERX964250">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964250</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#82</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#82</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053242, constructed from sample accession ERS633508 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633508" refname="UOS_IPD_189-sc-2201339" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633508</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_189-sc-2201339</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053242</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#83" center_name="The Wellcome Trust Sanger Institute" accession="ERX964251">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964251</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#83</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#83</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053254, constructed from sample accession ERS633510 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence GCTCCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633510" refname="UOS_IPD_190-sc-2201340" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633510</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_190-sc-2201340</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053254</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#84" center_name="The Wellcome Trust Sanger Institute" accession="ERX964252">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964252</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#84</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#84</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053266, constructed from sample accession ERS633511 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence GTAAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633511" refname="UOS_IPD_191-sc-2201341" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633511</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_191-sc-2201341</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053266</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#85" center_name="The Wellcome Trust Sanger Institute" accession="ERX964253">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964253</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#85</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#85</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053278, constructed from sample accession ERS633512 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence GAGGATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633512" refname="UOS_IPD_192-sc-2201342" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633512</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_192-sc-2201342</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053278</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#86" center_name="The Wellcome Trust Sanger Institute" accession="ERX964254">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964254</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#86</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053290, constructed from sample accession ERS633513 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence GTTGTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633513" refname="UOS_IPD_193-sc-2201343" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633513</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_193-sc-2201343</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053290</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#87" center_name="The Wellcome Trust Sanger Institute" accession="ERX964255">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964255</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#87</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053302, constructed from sample accession ERS633514 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence GGATTAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633514" refname="UOS_IPD_194-sc-2201344" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633514</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_194-sc-2201344</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053302</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#88" center_name="The Wellcome Trust Sanger Institute" accession="ERX964256">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964256</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#88</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#88</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053314, constructed from sample accession ERS633515 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence GATAGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633515" refname="UOS_IPD_196-sc-2201345" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633515</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_196-sc-2201345</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053314</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#89" center_name="The Wellcome Trust Sanger Institute" accession="ERX964257">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964257</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#89</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#89</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053231, constructed from sample accession ERS633516 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence GTGTGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633516" refname="UOS_IPD_198-sc-2201346" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633516</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_198-sc-2201346</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053231</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#90" center_name="The Wellcome Trust Sanger Institute" accession="ERX964258">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964258</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#90</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#90</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053243, constructed from sample accession ERS633517 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence GCAATCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633517" refname="UOS_IPD_203-sc-2201347" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633517</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_203-sc-2201347</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053243</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#91" center_name="The Wellcome Trust Sanger Institute" accession="ERX964259">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964259</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#91</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#91</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053255, constructed from sample accession ERS633518 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence GACCTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633518" refname="UOS_IPD_204-sc-2201348" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633518</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_204-sc-2201348</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053255</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_7#2" center_name="The Wellcome Trust Sanger Institute" accession="ERX964260">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964260</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053329, constructed from sample accession ERS633520 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633520" refname="UOS_IPD_206-sc-2201350" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633520</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_206-sc-2201350</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053329</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#3" center_name="The Wellcome Trust Sanger Institute" accession="ERX964261">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964261</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053341, constructed from sample accession ERS633521 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633521" refname="UOS_IPD_207-sc-2201351" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633521</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_207-sc-2201351</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053341</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#4" center_name="The Wellcome Trust Sanger Institute" accession="ERX964262">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964262</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053353, constructed from sample accession ERS633522 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633522" refname="UOS_IPD_208-sc-2201352" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633522</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_208-sc-2201352</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053353</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#5" center_name="The Wellcome Trust Sanger Institute" accession="ERX964263">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964263</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053365, constructed from sample accession ERS633523 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633523" refname="UOS_IPD_209-sc-2201353" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633523</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_209-sc-2201353</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053365</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#6" center_name="The Wellcome Trust Sanger Institute" accession="ERX964264">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964264</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053377, constructed from sample accession ERS633524 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633524" refname="UOS_IPD_210-sc-2201354" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633524</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_210-sc-2201354</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053377</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX964265">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964265</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053401, constructed from sample accession ERS633526 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633526" refname="UOS_IPD_212-sc-2201356" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633526</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_212-sc-2201356</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053401</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#9" center_name="The Wellcome Trust Sanger Institute" accession="ERX964266">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964266</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053318, constructed from sample accession ERS633527 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633527" refname="UOS_IPD_213-sc-2201357" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633527</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_213-sc-2201357</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053318</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#10" center_name="The Wellcome Trust Sanger Institute" accession="ERX964267">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964267</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053330, constructed from sample accession ERS633528 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633528" refname="UOS_IPD_214-sc-2201358" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633528</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_214-sc-2201358</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053330</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#11" center_name="The Wellcome Trust Sanger Institute" accession="ERX964268">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964268</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053342, constructed from sample accession ERS633529 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633529" refname="UOS_IPD_215-sc-2201359" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633529</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_215-sc-2201359</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053342</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#12" center_name="The Wellcome Trust Sanger Institute" accession="ERX964269">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964269</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053354, constructed from sample accession ERS633530 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633530" refname="UOS_IPD_216-sc-2201360" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633530</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_216-sc-2201360</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053354</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#13" center_name="The Wellcome Trust Sanger Institute" accession="ERX964270">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964270</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053366, constructed from sample accession ERS633531 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633531" refname="UOS_IPD_217-sc-2201361" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633531</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_217-sc-2201361</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053366</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#14" center_name="The Wellcome Trust Sanger Institute" accession="ERX964271">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964271</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053378, constructed from sample accession ERS633532 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633532" refname="UOS_IPD_218-sc-2201362" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633532</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_218-sc-2201362</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053378</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#15" center_name="The Wellcome Trust Sanger Institute" accession="ERX964272">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964272</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053390, constructed from sample accession ERS633533 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633533" refname="UOS_IPD_219-sc-2201363" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633533</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_219-sc-2201363</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053390</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#16" center_name="The Wellcome Trust Sanger Institute" accession="ERX964273">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964273</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053402, constructed from sample accession ERS633534 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633534" refname="UOS_IPD_220-sc-2201364" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633534</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_220-sc-2201364</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053402</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#17" center_name="The Wellcome Trust Sanger Institute" accession="ERX964274">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964274</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053319, constructed from sample accession ERS633535 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633535" refname="UOS_IPD_221-sc-2201365" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633535</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_221-sc-2201365</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053319</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#18" center_name="The Wellcome Trust Sanger Institute" accession="ERX964275">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964275</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053331, constructed from sample accession ERS633536 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633536" refname="UOS_IPD_222-sc-2201366" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633536</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_222-sc-2201366</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053331</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#19" center_name="The Wellcome Trust Sanger Institute" accession="ERX964276">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964276</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053343, constructed from sample accession ERS633537 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633537" refname="UOS_IPD_223-sc-2201367" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633537</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_223-sc-2201367</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053343</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#20" center_name="The Wellcome Trust Sanger Institute" accession="ERX964277">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964277</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053355, constructed from sample accession ERS633538 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633538" refname="UOS_IPD_224-sc-2201368" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633538</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_224-sc-2201368</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053355</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#21" center_name="The Wellcome Trust Sanger Institute" accession="ERX964278">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964278</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053367, constructed from sample accession ERS633539 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633539" refname="UOS_IPD_225-sc-2201369" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633539</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_225-sc-2201369</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053367</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#22" center_name="The Wellcome Trust Sanger Institute" accession="ERX964279">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964279</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053379, constructed from sample accession ERS633540 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633540" refname="UOS_IPD_226-sc-2201370" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633540</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_226-sc-2201370</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053379</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#23" center_name="The Wellcome Trust Sanger Institute" accession="ERX964280">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964280</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053391, constructed from sample accession ERS633541 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633541" refname="UOS_IPD_227-sc-2201371" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633541</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_227-sc-2201371</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053391</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#24" center_name="The Wellcome Trust Sanger Institute" accession="ERX964281">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964281</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053403, constructed from sample accession ERS633542 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633542" refname="UOS_IPD_228-sc-2201372" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633542</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_228-sc-2201372</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053403</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#25" center_name="The Wellcome Trust Sanger Institute" accession="ERX964282">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964282</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053320, constructed from sample accession ERS633543 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633543" refname="UOS_IPD_229-sc-2201373" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633543</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_229-sc-2201373</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053320</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#26" center_name="The Wellcome Trust Sanger Institute" accession="ERX964283">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964283</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053332, constructed from sample accession ERS633544 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633544" refname="UOS_IPD_230-sc-2201374" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633544</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_230-sc-2201374</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053332</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#27" center_name="The Wellcome Trust Sanger Institute" accession="ERX964284">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964284</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053344, constructed from sample accession ERS633545 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633545" refname="UOS_IPD_231-sc-2201375" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633545</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_231-sc-2201375</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053344</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#28" center_name="The Wellcome Trust Sanger Institute" accession="ERX964285">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964285</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053356, constructed from sample accession ERS633546 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633546" refname="UOS_IPD_232-sc-2201376" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633546</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_232-sc-2201376</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053356</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#29" center_name="The Wellcome Trust Sanger Institute" accession="ERX964286">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964286</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053368, constructed from sample accession ERS633547 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633547" refname="UOS_IPD_233-sc-2201377" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633547</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_233-sc-2201377</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053368</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#30" center_name="The Wellcome Trust Sanger Institute" accession="ERX964287">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964287</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053380, constructed from sample accession ERS633548 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633548" refname="UOS_IPD_234-sc-2201378" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633548</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_234-sc-2201378</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053380</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX964288">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964288</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053392, constructed from sample accession ERS633549 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633549" refname="UOS_IPD_235-sc-2201379" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633549</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_235-sc-2201379</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053392</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX964289">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964289</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053404, constructed from sample accession ERS633550 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633550" refname="UOS_IPD_236-sc-2201380" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633550</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_236-sc-2201380</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053404</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX964290">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964290</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053321, constructed from sample accession ERS633551 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633551" refname="UOS_IPD_237-sc-2201381" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633551</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_237-sc-2201381</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053321</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX964291">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964291</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053333, constructed from sample accession ERS633552 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633552" refname="UOS_IPD_238-sc-2201382" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633552</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_238-sc-2201382</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053333</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX964292">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964292</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053345, constructed from sample accession ERS633553 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633553" refname="UOS_IPD_239-sc-2201383" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633553</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_239-sc-2201383</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053345</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX964293">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964293</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053357, constructed from sample accession ERS633554 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633554" refname="UOS_IPD_241-sc-2201384" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633554</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_241-sc-2201384</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053357</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX964294">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964294</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053369, constructed from sample accession ERS633555 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633555" refname="UOS_IPD_243-sc-2201385" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633555</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_243-sc-2201385</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053369</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX964295">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964295</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053381, constructed from sample accession ERS633556 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633556" refname="UOS_IPD_245-sc-2201386" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633556</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_245-sc-2201386</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053381</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_5#44" center_name="The Wellcome Trust Sanger Institute" accession="ERX964123">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964123</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#44</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041592, constructed from sample accession ERS633385 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633385" refname="UOS_IPD_12-sc-2201215" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633385</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_12-sc-2201215</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041592</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#45" center_name="The Wellcome Trust Sanger Institute" accession="ERX964124">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964124</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#45</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041604, constructed from sample accession ERS633411 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633411" refname="UOS_IPD_48-sc-2201240" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633411</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_48-sc-2201240</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041604</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#46" center_name="The Wellcome Trust Sanger Institute" accession="ERX964125">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964125</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#46</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041616, constructed from sample accession ERS633451 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633451" refname="UOS_IPD_103-sc-2201279" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633451</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_103-sc-2201279</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041616</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#47" center_name="The Wellcome Trust Sanger Institute" accession="ERX964126">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964126</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#47</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041628, constructed from sample accession ERS633453 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633453" refname="UOS_IPD_105-sc-2201281" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633453</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_105-sc-2201281</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041628</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#48" center_name="The Wellcome Trust Sanger Institute" accession="ERX964127">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964127</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#48</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041640, constructed from sample accession ERS633576 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633576" refname="UOS_IPD_274-sc-2201408" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633576</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_274-sc-2201408</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041640</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#49" center_name="The Wellcome Trust Sanger Institute" accession="ERX964128">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964128</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#49</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041557, constructed from sample accession ERS633658 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633658" refname="UOS_IPD_400-sc-2201489" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633658</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_400-sc-2201489</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041557</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#50" center_name="The Wellcome Trust Sanger Institute" accession="ERX964129">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964129</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#50</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041569, constructed from sample accession ERS633379 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633379" refname="UOS_IPD_2-sc-2201209" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633379</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_2-sc-2201209</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041569</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#51" center_name="The Wellcome Trust Sanger Institute" accession="ERX964130">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964130</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#51</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041581, constructed from sample accession ERS633380 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633380" refname="UOS_IPD_6-sc-2201210" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633380</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_6-sc-2201210</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041581</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#52" center_name="The Wellcome Trust Sanger Institute" accession="ERX964131">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964131</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#52</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041593, constructed from sample accession ERS633381 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633381" refname="UOS_IPD_8-sc-2201211" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633381</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_8-sc-2201211</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041593</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#53" center_name="The Wellcome Trust Sanger Institute" accession="ERX964132">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964132</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#53</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041605, constructed from sample accession ERS633382 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633382" refname="UOS_IPD_9-sc-2201212" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633382</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_9-sc-2201212</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041605</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#54" center_name="The Wellcome Trust Sanger Institute" accession="ERX964133">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964133</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#54</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041617, constructed from sample accession ERS633383 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633383" refname="UOS_IPD_10-sc-2201213" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633383</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_10-sc-2201213</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041617</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#55" center_name="The Wellcome Trust Sanger Institute" accession="ERX964134">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964134</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#55</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041629, constructed from sample accession ERS633384 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633384" refname="UOS_IPD_11-sc-2201214" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633384</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_11-sc-2201214</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041629</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#56" center_name="The Wellcome Trust Sanger Institute" accession="ERX964135">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964135</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#56</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041641, constructed from sample accession ERS633386 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633386" refname="UOS_IPD_14-sc-2201216" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633386</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_14-sc-2201216</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041641</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#57" center_name="The Wellcome Trust Sanger Institute" accession="ERX964136">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964136</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#57</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041558, constructed from sample accession ERS633387 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633387" refname="UOS_IPD_16-sc-2201217" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633387</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_16-sc-2201217</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041558</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#59" center_name="The Wellcome Trust Sanger Institute" accession="ERX964137">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964137</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#59</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041582, constructed from sample accession ERS633389 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633389" refname="UOS_IPD_18-sc-2201219" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633389</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_18-sc-2201219</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041582</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#61" center_name="The Wellcome Trust Sanger Institute" accession="ERX964138">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964138</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#61</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041606, constructed from sample accession ERS633391 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633391" refname="UOS_IPD_20-sc-2201221" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633391</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_20-sc-2201221</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041606</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#62" center_name="The Wellcome Trust Sanger Institute" accession="ERX964139">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964139</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#62</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041618, constructed from sample accession ERS633392 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633392" refname="UOS_IPD_24-sc-2201222" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633392</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_24-sc-2201222</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041618</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#63" center_name="The Wellcome Trust Sanger Institute" accession="ERX964140">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964140</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#63</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#63</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041630, constructed from sample accession ERS633393 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633393" refname="UOS_IPD_25-sc-2201223" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633393</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_25-sc-2201223</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041630</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#64" center_name="The Wellcome Trust Sanger Institute" accession="ERX964141">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964141</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#64</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#64</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041642, constructed from sample accession ERS633394 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633394" refname="UOS_IPD_26-sc-2201224" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633394</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_26-sc-2201224</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041642</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#65" center_name="The Wellcome Trust Sanger Institute" accession="ERX964142">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964142</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#65</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#65</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041559, constructed from sample accession ERS633395 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633395" refname="UOS_IPD_27-sc-2201225" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633395</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_27-sc-2201225</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041559</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#66" center_name="The Wellcome Trust Sanger Institute" accession="ERX964143">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964143</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#66</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#66</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041571, constructed from sample accession ERS633396 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633396" refname="UOS_IPD_28-sc-2201226" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633396</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_28-sc-2201226</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041571</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#67" center_name="The Wellcome Trust Sanger Institute" accession="ERX964144">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964144</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#67</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041583, constructed from sample accession ERS633397 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633397" refname="UOS_IPD_29-sc-2201227" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633397</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_29-sc-2201227</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041583</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#68" center_name="The Wellcome Trust Sanger Institute" accession="ERX964145">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964145</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#68</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041595, constructed from sample accession ERS633398 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633398" refname="UOS_IPD_30-sc-2201228" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633398</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_30-sc-2201228</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041595</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#69" center_name="The Wellcome Trust Sanger Institute" accession="ERX964146">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964146</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#69</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#69</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041607, constructed from sample accession ERS633399 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633399" refname="UOS_IPD_33-sc-2201229" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633399</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_33-sc-2201229</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041607</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#70" center_name="The Wellcome Trust Sanger Institute" accession="ERX964147">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964147</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#70</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#70</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041619, constructed from sample accession ERS633400 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633400" refname="UOS_IPD_35-sc-2201230" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633400</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_35-sc-2201230</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041619</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#71" center_name="The Wellcome Trust Sanger Institute" accession="ERX964148">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964148</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#71</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#71</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041631, constructed from sample accession ERS633401 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence GTGTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633401" refname="UOS_IPD_36-sc-2201231" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633401</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_36-sc-2201231</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041631</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#72" center_name="The Wellcome Trust Sanger Institute" accession="ERX964149">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964149</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#72</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#72</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041643, constructed from sample accession ERS633402 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence GACGGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633402" refname="UOS_IPD_38-sc-2201232" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633402</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_38-sc-2201232</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041643</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#73" center_name="The Wellcome Trust Sanger Institute" accession="ERX964150">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964150</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#73</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#73</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041560, constructed from sample accession ERS633403 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633403" refname="UOS_IPD_40-sc-2201233" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633403</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_40-sc-2201233</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041560</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#74" center_name="The Wellcome Trust Sanger Institute" accession="ERX964151">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964151</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#74</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041572, constructed from sample accession ERS633404 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633404" refname="UOS_IPD_42-sc-2201234" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633404</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_42-sc-2201234</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041572</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#75" center_name="The Wellcome Trust Sanger Institute" accession="ERX964152">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964152</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#75</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041584, constructed from sample accession ERS633405 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence GAATCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633405" refname="UOS_IPD_43-sc-2201235" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633405</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_43-sc-2201235</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041584</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#76" center_name="The Wellcome Trust Sanger Institute" accession="ERX964153">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964153</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#76</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041596, constructed from sample accession ERS633406 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633406" refname="UOS_IPD_44-sc-2201236" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633406</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_44-sc-2201236</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041596</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#77" center_name="The Wellcome Trust Sanger Institute" accession="ERX964154">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964154</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#77</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041608, constructed from sample accession ERS633408 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633408" refname="UOS_IPD_45-sc-2201237" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633408</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_45-sc-2201237</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041608</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#78" center_name="The Wellcome Trust Sanger Institute" accession="ERX964155">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964155</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#78</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#78</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041620, constructed from sample accession ERS633409 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633409" refname="UOS_IPD_46-sc-2201238" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633409</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_46-sc-2201238</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041620</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#79" center_name="The Wellcome Trust Sanger Institute" accession="ERX964156">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964156</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#79</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041632, constructed from sample accession ERS633410 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633410" refname="UOS_IPD_47-sc-2201239" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633410</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_47-sc-2201239</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041632</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#80" center_name="The Wellcome Trust Sanger Institute" accession="ERX964157">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964157</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#80</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041644, constructed from sample accession ERS633412 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence GTCGCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633412" refname="UOS_IPD_49-sc-2201241" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633412</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_49-sc-2201241</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041644</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#81" center_name="The Wellcome Trust Sanger Institute" accession="ERX964158">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964158</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#81</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041561, constructed from sample accession ERS633413 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633413" refname="UOS_IPD_50-sc-2201242" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633413</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_50-sc-2201242</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041561</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#82" center_name="The Wellcome Trust Sanger Institute" accession="ERX964159">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964159</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#82</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#82</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041573, constructed from sample accession ERS633414 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633414" refname="UOS_IPD_51-sc-2201243" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633414</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_51-sc-2201243</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041573</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#83" center_name="The Wellcome Trust Sanger Institute" accession="ERX964160">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964160</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#83</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#83</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041585, constructed from sample accession ERS633415 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence GCTCCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633415" refname="UOS_IPD_52-sc-2201244" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633415</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_52-sc-2201244</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041585</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#84" center_name="The Wellcome Trust Sanger Institute" accession="ERX964161">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964161</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#84</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#84</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041597, constructed from sample accession ERS633416 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence GTAAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633416" refname="UOS_IPD_53-sc-2201245" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633416</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_53-sc-2201245</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041597</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#85" center_name="The Wellcome Trust Sanger Institute" accession="ERX964162">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964162</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#85</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#85</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041609, constructed from sample accession ERS633417 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence GAGGATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633417" refname="UOS_IPD_56-sc-2201246" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633417</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_56-sc-2201246</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041609</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#86" center_name="The Wellcome Trust Sanger Institute" accession="ERX964163">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964163</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#86</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041621, constructed from sample accession ERS633418 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence GTTGTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633418" refname="UOS_IPD_57-sc-2201247" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633418</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_57-sc-2201247</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041621</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#87" center_name="The Wellcome Trust Sanger Institute" accession="ERX964164">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964164</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#87</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041633, constructed from sample accession ERS633419 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence GGATTAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633419" refname="UOS_IPD_59-sc-2201248" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633419</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_59-sc-2201248</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041633</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#88" center_name="The Wellcome Trust Sanger Institute" accession="ERX964165">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964165</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#88</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#88</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041645, constructed from sample accession ERS633420 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence GATAGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633420" refname="UOS_IPD_60-sc-2201249" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633420</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_60-sc-2201249</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041645</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#89" center_name="The Wellcome Trust Sanger Institute" accession="ERX964166">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964166</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#89</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#89</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041562, constructed from sample accession ERS633421 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence GTGTGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633421" refname="UOS_IPD_61-sc-2201250" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633421</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_61-sc-2201250</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041562</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#90" center_name="The Wellcome Trust Sanger Institute" accession="ERX964167">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964167</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#90</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#90</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041574, constructed from sample accession ERS633422 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence GCAATCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633422" refname="UOS_IPD_62-sc-2201251" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633422</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_62-sc-2201251</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041574</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_5#91" center_name="The Wellcome Trust Sanger Institute" accession="ERX964168">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964168</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_5#91</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_5#91</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13041586, constructed from sample accession ERS633423 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_5).  This submission includes reads tagged with the sequence GACCTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633423" refname="UOS_IPD_64-sc-2201252" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633423</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_64-sc-2201252</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13041586</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#1" center_name="The Wellcome Trust Sanger Institute" accession="ERX964169">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964169</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053220, constructed from sample accession ERS633424 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633424" refname="UOS_IPD_66-sc-2201253" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633424</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_66-sc-2201253</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053220</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#2" center_name="The Wellcome Trust Sanger Institute" accession="ERX964170">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964170</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053232, constructed from sample accession ERS633425 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633425" refname="UOS_IPD_68-sc-2201254" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633425</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_68-sc-2201254</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053232</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#3" center_name="The Wellcome Trust Sanger Institute" accession="ERX964171">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964171</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053244, constructed from sample accession ERS633426 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633426" refname="UOS_IPD_74-sc-2201255" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633426</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_74-sc-2201255</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053244</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#4" center_name="The Wellcome Trust Sanger Institute" accession="ERX964172">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964172</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053256, constructed from sample accession ERS633427 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633427" refname="UOS_IPD_75-sc-2201256" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633427</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_75-sc-2201256</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053256</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#5" center_name="The Wellcome Trust Sanger Institute" accession="ERX964173">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964173</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053268, constructed from sample accession ERS633428 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633428" refname="UOS_IPD_76-sc-2201257" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633428</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_76-sc-2201257</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053268</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#6" center_name="The Wellcome Trust Sanger Institute" accession="ERX964174">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964174</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053280, constructed from sample accession ERS633429 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633429" refname="UOS_IPD_79-sc-2201258" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633429</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_79-sc-2201258</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053280</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#7" center_name="The Wellcome Trust Sanger Institute" accession="ERX964175">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964175</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053292, constructed from sample accession ERS633430 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633430" refname="UOS_IPD_81-sc-2201259" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633430</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_81-sc-2201259</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053292</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX964176">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964176</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053304, constructed from sample accession ERS633431 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633431" refname="UOS_IPD_82-sc-2201260" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633431</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_82-sc-2201260</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053304</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#9" center_name="The Wellcome Trust Sanger Institute" accession="ERX964177">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964177</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053221, constructed from sample accession ERS633432 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633432" refname="UOS_IPD_83-sc-2201261" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633432</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_83-sc-2201261</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053221</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#10" center_name="The Wellcome Trust Sanger Institute" accession="ERX964178">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964178</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053233, constructed from sample accession ERS633433 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633433" refname="UOS_IPD_84-sc-2201262" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633433</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_84-sc-2201262</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053233</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#11" center_name="The Wellcome Trust Sanger Institute" accession="ERX964179">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964179</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053245, constructed from sample accession ERS633434 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633434" refname="UOS_IPD_85-sc-2201263" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633434</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_85-sc-2201263</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053245</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#12" center_name="The Wellcome Trust Sanger Institute" accession="ERX964180">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964180</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053257, constructed from sample accession ERS633435 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633435" refname="UOS_IPD_86-sc-2201264" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633435</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_86-sc-2201264</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053257</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#13" center_name="The Wellcome Trust Sanger Institute" accession="ERX964181">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964181</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053269, constructed from sample accession ERS633436 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633436" refname="UOS_IPD_87-sc-2201265" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633436</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_87-sc-2201265</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053269</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#14" center_name="The Wellcome Trust Sanger Institute" accession="ERX964182">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964182</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053281, constructed from sample accession ERS633437 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633437" refname="UOS_IPD_88-sc-2201266" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633437</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_88-sc-2201266</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053281</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#15" center_name="The Wellcome Trust Sanger Institute" accession="ERX964183">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964183</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053293, constructed from sample accession ERS633438 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633438" refname="UOS_IPD_89-sc-2201267" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633438</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_89-sc-2201267</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053293</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#16" center_name="The Wellcome Trust Sanger Institute" accession="ERX964184">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964184</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053305, constructed from sample accession ERS633439 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633439" refname="UOS_IPD_90-sc-2201268" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633439</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_90-sc-2201268</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053305</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#17" center_name="The Wellcome Trust Sanger Institute" accession="ERX964185">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964185</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053222, constructed from sample accession ERS633441 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633441" refname="UOS_IPD_91-sc-2201269" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633441</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_91-sc-2201269</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053222</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#18" center_name="The Wellcome Trust Sanger Institute" accession="ERX964186">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964186</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053234, constructed from sample accession ERS633442 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633442" refname="UOS_IPD_92-sc-2201270" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633442</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_92-sc-2201270</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053234</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#19" center_name="The Wellcome Trust Sanger Institute" accession="ERX964187">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964187</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053246, constructed from sample accession ERS633443 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633443" refname="UOS_IPD_93-sc-2201271" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633443</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_93-sc-2201271</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053246</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#20" center_name="The Wellcome Trust Sanger Institute" accession="ERX964188">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964188</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053258, constructed from sample accession ERS633444 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633444" refname="UOS_IPD_95-sc-2201272" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633444</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_95-sc-2201272</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053258</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#21" center_name="The Wellcome Trust Sanger Institute" accession="ERX964189">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964189</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053270, constructed from sample accession ERS633445 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633445" refname="UOS_IPD_96-sc-2201273" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633445</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_96-sc-2201273</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053270</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#22" center_name="The Wellcome Trust Sanger Institute" accession="ERX964190">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964190</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053282, constructed from sample accession ERS633446 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633446" refname="UOS_IPD_97-sc-2201274" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633446</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_97-sc-2201274</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053282</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#23" center_name="The Wellcome Trust Sanger Institute" accession="ERX964191">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964191</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053294, constructed from sample accession ERS633447 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633447" refname="UOS_IPD_98-sc-2201275" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633447</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_98-sc-2201275</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053294</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#24" center_name="The Wellcome Trust Sanger Institute" accession="ERX964192">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964192</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053306, constructed from sample accession ERS633448 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633448" refname="UOS_IPD_99-sc-2201276" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633448</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_99-sc-2201276</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053306</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#25" center_name="The Wellcome Trust Sanger Institute" accession="ERX964193">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964193</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053223, constructed from sample accession ERS633449 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633449" refname="UOS_IPD_100-sc-2201277" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633449</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_100-sc-2201277</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053223</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#26" center_name="The Wellcome Trust Sanger Institute" accession="ERX964194">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964194</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053235, constructed from sample accession ERS633450 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633450" refname="UOS_IPD_101-sc-2201278" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633450</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_101-sc-2201278</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053235</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#27" center_name="The Wellcome Trust Sanger Institute" accession="ERX964195">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964195</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053247, constructed from sample accession ERS633452 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633452" refname="UOS_IPD_104-sc-2201280" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633452</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_104-sc-2201280</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053247</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#28" center_name="The Wellcome Trust Sanger Institute" accession="ERX964196">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964196</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053259, constructed from sample accession ERS633454 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633454" refname="UOS_IPD_106-sc-2201282" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633454</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_106-sc-2201282</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053259</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#29" center_name="The Wellcome Trust Sanger Institute" accession="ERX964197">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964197</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053271, constructed from sample accession ERS633455 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633455" refname="UOS_IPD_107-sc-2201283" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633455</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_107-sc-2201283</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053271</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#30" center_name="The Wellcome Trust Sanger Institute" accession="ERX964198">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964198</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053283, constructed from sample accession ERS633456 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633456" refname="UOS_IPD_108-sc-2201284" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633456</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_108-sc-2201284</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053283</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX964199">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964199</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053295, constructed from sample accession ERS633457 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633457" refname="UOS_IPD_109-sc-2201285" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633457</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_109-sc-2201285</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053295</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX964200">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964200</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053307, constructed from sample accession ERS633458 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633458" refname="UOS_IPD_110-sc-2201286" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633458</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_110-sc-2201286</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053307</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX964201">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964201</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053224, constructed from sample accession ERS633459 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633459" refname="UOS_IPD_111-sc-2201287" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633459</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_111-sc-2201287</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053224</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX964202">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964202</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053236, constructed from sample accession ERS633460 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633460" refname="UOS_IPD_112-sc-2201288" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633460</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_112-sc-2201288</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053236</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX964203">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964203</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053248, constructed from sample accession ERS633461 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633461" refname="UOS_IPD_113-sc-2201289" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633461</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_113-sc-2201289</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053248</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX964204">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964204</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053260, constructed from sample accession ERS633462 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633462" refname="UOS_IPD_114-sc-2201290" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633462</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_114-sc-2201290</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053260</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX964205">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964205</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053272, constructed from sample accession ERS633463 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633463" refname="UOS_IPD_116-sc-2201291" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633463</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_116-sc-2201291</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053272</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX964206">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964206</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053284, constructed from sample accession ERS633464 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633464" refname="UOS_IPD_117-sc-2201292" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633464</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_117-sc-2201292</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053284</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#39" center_name="The Wellcome Trust Sanger Institute" accession="ERX964207">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964207</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#39</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053296, constructed from sample accession ERS633465 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633465" refname="UOS_IPD_118-sc-2201293" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633465</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_118-sc-2201293</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053296</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#40" center_name="The Wellcome Trust Sanger Institute" accession="ERX964208">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964208</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#40</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053308, constructed from sample accession ERS633466 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633466" refname="UOS_IPD_119-sc-2201294" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633466</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_119-sc-2201294</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053308</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#41" center_name="The Wellcome Trust Sanger Institute" accession="ERX964209">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964209</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#41</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053225, constructed from sample accession ERS633467 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633467" refname="UOS_IPD_120-sc-2201295" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633467</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_120-sc-2201295</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053225</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#42" center_name="The Wellcome Trust Sanger Institute" accession="ERX964210">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964210</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#42</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053237, constructed from sample accession ERS633468 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633468" refname="UOS_IPD_121-sc-2201296" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633468</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_121-sc-2201296</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053237</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#43" center_name="The Wellcome Trust Sanger Institute" accession="ERX964211">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964211</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#43</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053249, constructed from sample accession ERS633469 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633469" refname="UOS_IPD_122-sc-2201297" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633469</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_122-sc-2201297</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053249</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#44" center_name="The Wellcome Trust Sanger Institute" accession="ERX964212">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964212</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#44</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053261, constructed from sample accession ERS633470 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633470" refname="UOS_IPD_123-sc-2201298" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633470</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_123-sc-2201298</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053261</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#45" center_name="The Wellcome Trust Sanger Institute" accession="ERX964213">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964213</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#45</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053273, constructed from sample accession ERS633471 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633471" refname="UOS_IPD_125-sc-2201299" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633471</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_125-sc-2201299</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053273</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#46" center_name="The Wellcome Trust Sanger Institute" accession="ERX964214">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964214</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#46</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053285, constructed from sample accession ERS633472 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633472" refname="UOS_IPD_126-sc-2201300" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633472</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_126-sc-2201300</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053285</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#47" center_name="The Wellcome Trust Sanger Institute" accession="ERX964215">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964215</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#47</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053297, constructed from sample accession ERS633473 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633473" refname="UOS_IPD_127-sc-2201301" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633473</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_127-sc-2201301</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053297</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#48" center_name="The Wellcome Trust Sanger Institute" accession="ERX964216">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964216</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#48</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053309, constructed from sample accession ERS633474 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633474" refname="UOS_IPD_131-sc-2201305" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633474</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_131-sc-2201305</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053309</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#49" center_name="The Wellcome Trust Sanger Institute" accession="ERX964217">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964217</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#49</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053226, constructed from sample accession ERS633475 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633475" refname="UOS_IPD_132-sc-2201306" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633475</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_132-sc-2201306</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053226</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#50" center_name="The Wellcome Trust Sanger Institute" accession="ERX964218">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964218</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#50</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053238, constructed from sample accession ERS633476 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633476" refname="UOS_IPD_133-sc-2201307" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633476</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_133-sc-2201307</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053238</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#51" center_name="The Wellcome Trust Sanger Institute" accession="ERX964219">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964219</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#51</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053250, constructed from sample accession ERS633477 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633477" refname="UOS_IPD_134-sc-2201308" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633477</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_134-sc-2201308</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053250</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#52" center_name="The Wellcome Trust Sanger Institute" accession="ERX964220">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964220</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#52</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053262, constructed from sample accession ERS633478 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633478" refname="UOS_IPD_136-sc-2201309" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633478</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_136-sc-2201309</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053262</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#53" center_name="The Wellcome Trust Sanger Institute" accession="ERX964221">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964221</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#53</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053274, constructed from sample accession ERS633479 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633479" refname="UOS_IPD_137-sc-2201310" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633479</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_137-sc-2201310</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053274</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#54" center_name="The Wellcome Trust Sanger Institute" accession="ERX964222">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964222</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#54</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053286, constructed from sample accession ERS633480 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633480" refname="UOS_IPD_138-sc-2201311" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633480</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_138-sc-2201311</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053286</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#55" center_name="The Wellcome Trust Sanger Institute" accession="ERX964223">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964223</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#55</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053298, constructed from sample accession ERS633481 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633481" refname="UOS_IPD_139-sc-2201312" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633481</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_139-sc-2201312</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053298</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#56" center_name="The Wellcome Trust Sanger Institute" accession="ERX964224">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964224</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#56</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053310, constructed from sample accession ERS633482 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633482" refname="UOS_IPD_140-sc-2201313" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633482</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_140-sc-2201313</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053310</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#57" center_name="The Wellcome Trust Sanger Institute" accession="ERX964225">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964225</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#57</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053227, constructed from sample accession ERS633483 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633483" refname="UOS_IPD_142-sc-2201314" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633483</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_142-sc-2201314</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053227</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#58" center_name="The Wellcome Trust Sanger Institute" accession="ERX964226">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964226</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#58</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053239, constructed from sample accession ERS633484 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633484" refname="UOS_IPD_143-sc-2201315" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633484</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_143-sc-2201315</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053239</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#59" center_name="The Wellcome Trust Sanger Institute" accession="ERX964227">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964227</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#59</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053251, constructed from sample accession ERS633485 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633485" refname="UOS_IPD_144-sc-2201316" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633485</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_144-sc-2201316</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053251</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#60" center_name="The Wellcome Trust Sanger Institute" accession="ERX964228">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964228</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#60</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#60</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053263, constructed from sample accession ERS633486 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633486" refname="UOS_IPD_145-sc-2201317" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633486</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_145-sc-2201317</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053263</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#61" center_name="The Wellcome Trust Sanger Institute" accession="ERX964229">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964229</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#61</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053275, constructed from sample accession ERS633487 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633487" refname="UOS_IPD_147-sc-2201318" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633487</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_147-sc-2201318</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053275</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#62" center_name="The Wellcome Trust Sanger Institute" accession="ERX964230">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964230</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#62</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053287, constructed from sample accession ERS633488 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633488" refname="UOS_IPD_160-sc-2201319" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633488</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_160-sc-2201319</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053287</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#63" center_name="The Wellcome Trust Sanger Institute" accession="ERX964231">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964231</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#63</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#63</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053299, constructed from sample accession ERS633489 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633489" refname="UOS_IPD_161-sc-2201320" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633489</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_161-sc-2201320</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053299</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#64" center_name="The Wellcome Trust Sanger Institute" accession="ERX964232">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964232</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#64</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#64</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053311, constructed from sample accession ERS633490 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633490" refname="UOS_IPD_162-sc-2201321" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633490</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_162-sc-2201321</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053311</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#65" center_name="The Wellcome Trust Sanger Institute" accession="ERX964233">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964233</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#65</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#65</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053228, constructed from sample accession ERS633491 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633491" refname="UOS_IPD_163-sc-2201322" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633491</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_163-sc-2201322</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053228</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#66" center_name="The Wellcome Trust Sanger Institute" accession="ERX964234">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964234</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#66</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#66</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053240, constructed from sample accession ERS633492 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633492" refname="UOS_IPD_164-sc-2201323" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633492</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_164-sc-2201323</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053240</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_6#67" center_name="The Wellcome Trust Sanger Institute" accession="ERX964235">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964235</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_6#67</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_6#67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053252, constructed from sample accession ERS633493 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_6).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633493" refname="UOS_IPD_165-sc-2201324" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633493</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_165-sc-2201324</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053252</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="225" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#80" center_name="The Wellcome Trust Sanger Institute" accession="ERX964428">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964428</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#80</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053708, constructed from sample accession ERS633694 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence GTCGCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633694" refname="UOS_IPD_465-sc-2201525" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633694</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_465-sc-2201525</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053708</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#81" center_name="The Wellcome Trust Sanger Institute" accession="ERX964429">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964429</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#81</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053625, constructed from sample accession ERS633695 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633695" refname="UOS_IPD_467-sc-2201526" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633695</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_467-sc-2201526</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053625</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_7#39" center_name="The Wellcome Trust Sanger Institute" accession="ERX964296">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964296</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#39</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053393, constructed from sample accession ERS633557 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633557" refname="UOS_IPD_246-sc-2201387" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633557</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_246-sc-2201387</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053393</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#40" center_name="The Wellcome Trust Sanger Institute" accession="ERX964297">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964297</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#40</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053405, constructed from sample accession ERS633558 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633558" refname="UOS_IPD_247-sc-2201388" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633558</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_247-sc-2201388</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053405</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#41" center_name="The Wellcome Trust Sanger Institute" accession="ERX964298">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964298</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#41</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053322, constructed from sample accession ERS633559 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633559" refname="UOS_IPD_248-sc-2201389" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633559</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_248-sc-2201389</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053322</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#42" center_name="The Wellcome Trust Sanger Institute" accession="ERX964299">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964299</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#42</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053334, constructed from sample accession ERS633560 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633560" refname="UOS_IPD_249-sc-2201390" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633560</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_249-sc-2201390</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053334</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#43" center_name="The Wellcome Trust Sanger Institute" accession="ERX964300">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964300</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#43</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053346, constructed from sample accession ERS633561 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633561" refname="UOS_IPD_250-sc-2201391" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633561</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_250-sc-2201391</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053346</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#44" center_name="The Wellcome Trust Sanger Institute" accession="ERX964301">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964301</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#44</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053358, constructed from sample accession ERS633562 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633562" refname="UOS_IPD_251-sc-2201392" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633562</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_251-sc-2201392</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053358</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#45" center_name="The Wellcome Trust Sanger Institute" accession="ERX964302">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964302</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#45</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053370, constructed from sample accession ERS633563 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633563" refname="UOS_IPD_252-sc-2201393" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633563</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_252-sc-2201393</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053370</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#46" center_name="The Wellcome Trust Sanger Institute" accession="ERX964303">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964303</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#46</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053382, constructed from sample accession ERS633564 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633564" refname="UOS_IPD_253-sc-2201394" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633564</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_253-sc-2201394</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053382</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#47" center_name="The Wellcome Trust Sanger Institute" accession="ERX964304">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964304</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#47</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053394, constructed from sample accession ERS633565 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633565" refname="UOS_IPD_254-sc-2201395" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633565</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_254-sc-2201395</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053394</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#48" center_name="The Wellcome Trust Sanger Institute" accession="ERX964305">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964305</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#48</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053406, constructed from sample accession ERS633566 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633566" refname="UOS_IPD_256-sc-2201396" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633566</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_256-sc-2201396</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053406</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#49" center_name="The Wellcome Trust Sanger Institute" accession="ERX964306">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964306</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#49</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053323, constructed from sample accession ERS633567 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633567" refname="UOS_IPD_257-sc-2201397" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633567</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_257-sc-2201397</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053323</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#50" center_name="The Wellcome Trust Sanger Institute" accession="ERX964307">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964307</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#50</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053335, constructed from sample accession ERS633568 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633568" refname="UOS_IPD_258-sc-2201398" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633568</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_258-sc-2201398</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053335</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#51" center_name="The Wellcome Trust Sanger Institute" accession="ERX964308">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964308</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#51</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053347, constructed from sample accession ERS633569 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633569" refname="UOS_IPD_259-sc-2201399" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633569</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_259-sc-2201399</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053347</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#52" center_name="The Wellcome Trust Sanger Institute" accession="ERX964309">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964309</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#52</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053359, constructed from sample accession ERS633570 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633570" refname="UOS_IPD_263-sc-2201402" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633570</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_263-sc-2201402</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053359</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#53" center_name="The Wellcome Trust Sanger Institute" accession="ERX964310">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964310</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#53</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053371, constructed from sample accession ERS633571 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633571" refname="UOS_IPD_264-sc-2201403" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633571</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_264-sc-2201403</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053371</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#54" center_name="The Wellcome Trust Sanger Institute" accession="ERX964311">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964311</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#54</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053383, constructed from sample accession ERS633572 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633572" refname="UOS_IPD_265-sc-2201404" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633572</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_265-sc-2201404</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053383</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#55" center_name="The Wellcome Trust Sanger Institute" accession="ERX964312">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964312</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#55</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053395, constructed from sample accession ERS633573 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633573" refname="UOS_IPD_271-sc-2201405" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633573</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_271-sc-2201405</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053395</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#56" center_name="The Wellcome Trust Sanger Institute" accession="ERX964313">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964313</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#56</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053407, constructed from sample accession ERS633574 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633574" refname="UOS_IPD_272-sc-2201406" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633574</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_272-sc-2201406</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053407</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#57" center_name="The Wellcome Trust Sanger Institute" accession="ERX964314">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964314</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#57</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053324, constructed from sample accession ERS633575 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633575" refname="UOS_IPD_273-sc-2201407" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633575</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_273-sc-2201407</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053324</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#58" center_name="The Wellcome Trust Sanger Institute" accession="ERX964315">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964315</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#58</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053336, constructed from sample accession ERS633577 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633577" refname="UOS_IPD_275-sc-2201409" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633577</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_275-sc-2201409</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053336</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#59" center_name="The Wellcome Trust Sanger Institute" accession="ERX964316">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964316</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#59</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053348, constructed from sample accession ERS633578 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633578" refname="UOS_IPD_276-sc-2201410" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633578</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_276-sc-2201410</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053348</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#60" center_name="The Wellcome Trust Sanger Institute" accession="ERX964317">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964317</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#60</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#60</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053360, constructed from sample accession ERS633579 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633579" refname="UOS_IPD_277-sc-2201411" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633579</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_277-sc-2201411</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053360</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#61" center_name="The Wellcome Trust Sanger Institute" accession="ERX964318">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964318</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#61</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053372, constructed from sample accession ERS633580 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633580" refname="UOS_IPD_278-sc-2201412" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633580</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_278-sc-2201412</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053372</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#62" center_name="The Wellcome Trust Sanger Institute" accession="ERX964319">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964319</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#62</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053384, constructed from sample accession ERS633581 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633581" refname="UOS_IPD_279-sc-2201413" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633581</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_279-sc-2201413</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053384</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#63" center_name="The Wellcome Trust Sanger Institute" accession="ERX964320">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964320</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#63</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#63</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053396, constructed from sample accession ERS633582 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633582" refname="UOS_IPD_280-sc-2201414" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633582</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_280-sc-2201414</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053396</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#64" center_name="The Wellcome Trust Sanger Institute" accession="ERX964321">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964321</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#64</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#64</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053408, constructed from sample accession ERS633583 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633583" refname="UOS_IPD_281-sc-2201415" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633583</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_281-sc-2201415</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053408</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#65" center_name="The Wellcome Trust Sanger Institute" accession="ERX964322">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964322</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#65</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#65</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053325, constructed from sample accession ERS633584 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633584" refname="UOS_IPD_282-sc-2201416" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633584</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_282-sc-2201416</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053325</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#66" center_name="The Wellcome Trust Sanger Institute" accession="ERX964323">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964323</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#66</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#66</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053337, constructed from sample accession ERS633585 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633585" refname="UOS_IPD_283-sc-2201417" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633585</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_283-sc-2201417</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053337</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#67" center_name="The Wellcome Trust Sanger Institute" accession="ERX964324">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964324</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#67</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053349, constructed from sample accession ERS633587 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633587" refname="UOS_IPD_284-sc-2201418" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633587</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_284-sc-2201418</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053349</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#68" center_name="The Wellcome Trust Sanger Institute" accession="ERX964325">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964325</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#68</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053361, constructed from sample accession ERS633588 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633588" refname="UOS_IPD_286-sc-2201419" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633588</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_286-sc-2201419</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053361</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#69" center_name="The Wellcome Trust Sanger Institute" accession="ERX964326">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964326</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#69</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#69</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053373, constructed from sample accession ERS633589 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633589" refname="UOS_IPD_287-sc-2201420" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633589</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_287-sc-2201420</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053373</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#70" center_name="The Wellcome Trust Sanger Institute" accession="ERX964327">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964327</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#70</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#70</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053385, constructed from sample accession ERS633590 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633590" refname="UOS_IPD_288-sc-2201421" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633590</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_288-sc-2201421</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053385</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#71" center_name="The Wellcome Trust Sanger Institute" accession="ERX964328">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964328</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#71</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#71</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053397, constructed from sample accession ERS633591 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence GTGTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633591" refname="UOS_IPD_289-sc-2201422" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633591</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_289-sc-2201422</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053397</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#72" center_name="The Wellcome Trust Sanger Institute" accession="ERX964329">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964329</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#72</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#72</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053409, constructed from sample accession ERS633592 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence GACGGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633592" refname="UOS_IPD_290-sc-2201423" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633592</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_290-sc-2201423</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053409</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#73" center_name="The Wellcome Trust Sanger Institute" accession="ERX964330">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964330</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#73</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#73</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053326, constructed from sample accession ERS633593 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633593" refname="UOS_IPD_291-sc-2201424" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633593</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_291-sc-2201424</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053326</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#74" center_name="The Wellcome Trust Sanger Institute" accession="ERX964331">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964331</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#74</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053338, constructed from sample accession ERS633594 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633594" refname="UOS_IPD_292-sc-2201425" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633594</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_292-sc-2201425</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053338</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#75" center_name="The Wellcome Trust Sanger Institute" accession="ERX964332">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964332</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#75</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053350, constructed from sample accession ERS633595 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence GAATCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633595" refname="UOS_IPD_293-sc-2201426" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633595</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_293-sc-2201426</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053350</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#76" center_name="The Wellcome Trust Sanger Institute" accession="ERX964333">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964333</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#76</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053362, constructed from sample accession ERS633596 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633596" refname="UOS_IPD_294-sc-2201427" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633596</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_294-sc-2201427</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053362</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#77" center_name="The Wellcome Trust Sanger Institute" accession="ERX964334">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964334</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#77</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053374, constructed from sample accession ERS633597 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633597" refname="UOS_IPD_296-sc-2201428" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633597</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_296-sc-2201428</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053374</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#78" center_name="The Wellcome Trust Sanger Institute" accession="ERX964335">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964335</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#78</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#78</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053386, constructed from sample accession ERS633598 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633598" refname="UOS_IPD_297-sc-2201429" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633598</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_297-sc-2201429</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053386</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#79" center_name="The Wellcome Trust Sanger Institute" accession="ERX964336">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964336</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#79</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053398, constructed from sample accession ERS633599 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633599" refname="UOS_IPD_298-sc-2201430" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633599</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_298-sc-2201430</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053398</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#80" center_name="The Wellcome Trust Sanger Institute" accession="ERX964337">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964337</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#80</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053410, constructed from sample accession ERS633600 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence GTCGCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633600" refname="UOS_IPD_299-sc-2201431" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633600</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_299-sc-2201431</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053410</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#81" center_name="The Wellcome Trust Sanger Institute" accession="ERX964338">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964338</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#81</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053327, constructed from sample accession ERS633601 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633601" refname="UOS_IPD_300-sc-2201432" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633601</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_300-sc-2201432</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053327</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#82" center_name="The Wellcome Trust Sanger Institute" accession="ERX964339">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964339</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#82</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#82</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053339, constructed from sample accession ERS633602 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633602" refname="UOS_IPD_302-sc-2201433" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633602</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_302-sc-2201433</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053339</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#83" center_name="The Wellcome Trust Sanger Institute" accession="ERX964340">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964340</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#83</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#83</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053351, constructed from sample accession ERS633603 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence GCTCCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633603" refname="UOS_IPD_303-sc-2201434" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633603</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_303-sc-2201434</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053351</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#84" center_name="The Wellcome Trust Sanger Institute" accession="ERX964341">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964341</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#84</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#84</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053363, constructed from sample accession ERS633604 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence GTAAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633604" refname="UOS_IPD_304-sc-2201435" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633604</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_304-sc-2201435</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053363</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#85" center_name="The Wellcome Trust Sanger Institute" accession="ERX964342">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964342</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#85</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#85</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053375, constructed from sample accession ERS633605 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence GAGGATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633605" refname="UOS_IPD_305-sc-2201436" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633605</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_305-sc-2201436</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053375</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#86" center_name="The Wellcome Trust Sanger Institute" accession="ERX964343">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964343</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#86</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053387, constructed from sample accession ERS633606 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence GTTGTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633606" refname="UOS_IPD_306-sc-2201437" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633606</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_306-sc-2201437</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053387</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#87" center_name="The Wellcome Trust Sanger Institute" accession="ERX964344">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964344</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#87</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053399, constructed from sample accession ERS633607 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence GGATTAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633607" refname="UOS_IPD_307-sc-2201438" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633607</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_307-sc-2201438</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053399</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#88" center_name="The Wellcome Trust Sanger Institute" accession="ERX964345">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964345</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#88</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#88</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053411, constructed from sample accession ERS633608 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence GATAGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633608" refname="UOS_IPD_308-sc-2201439" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633608</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_308-sc-2201439</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053411</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#89" center_name="The Wellcome Trust Sanger Institute" accession="ERX964346">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964346</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#89</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#89</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053328, constructed from sample accession ERS633610 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence GTGTGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633610" refname="UOS_IPD_309-sc-2201440" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633610</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_309-sc-2201440</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053328</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#90" center_name="The Wellcome Trust Sanger Institute" accession="ERX964347">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964347</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#90</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#90</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053340, constructed from sample accession ERS633611 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence GCAATCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633611" refname="UOS_IPD_311-sc-2201441" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633611</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_311-sc-2201441</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053340</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_7#91" center_name="The Wellcome Trust Sanger Institute" accession="ERX964348">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964348</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_7#91</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_7#91</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053352, constructed from sample accession ERS633612 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_7).  This submission includes reads tagged with the sequence GACCTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633612" refname="UOS_IPD_314-sc-2201442" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633612</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_314-sc-2201442</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053352</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="220" 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_15682_8#1" center_name="The Wellcome Trust Sanger Institute" accession="ERX964349">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964349</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053615, constructed from sample accession ERS633613 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633613" refname="UOS_IPD_315-sc-2201443" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633613</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_315-sc-2201443</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053615</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#2" center_name="The Wellcome Trust Sanger Institute" accession="ERX964350">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964350</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053627, constructed from sample accession ERS633614 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633614" refname="UOS_IPD_316-sc-2201444" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633614</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_316-sc-2201444</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053627</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#3" center_name="The Wellcome Trust Sanger Institute" accession="ERX964351">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964351</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053639, constructed from sample accession ERS633615 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633615" refname="UOS_IPD_318-sc-2201445" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633615</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_318-sc-2201445</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053639</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#4" center_name="The Wellcome Trust Sanger Institute" accession="ERX964352">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964352</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053651, constructed from sample accession ERS633616 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633616" refname="UOS_IPD_319-sc-2201446" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633616</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_319-sc-2201446</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053651</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#5" center_name="The Wellcome Trust Sanger Institute" accession="ERX964353">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964353</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053663, constructed from sample accession ERS633617 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633617" refname="UOS_IPD_320-sc-2201447" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633617</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_320-sc-2201447</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053663</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#6" center_name="The Wellcome Trust Sanger Institute" accession="ERX964354">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964354</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053675, constructed from sample accession ERS633618 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633618" refname="UOS_IPD_321-sc-2201448" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633618</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_321-sc-2201448</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053675</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#7" center_name="The Wellcome Trust Sanger Institute" accession="ERX964355">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964355</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053687, constructed from sample accession ERS633619 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633619" refname="UOS_IPD_323-sc-2201449" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633619</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_323-sc-2201449</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053687</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX964356">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964356</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053699, constructed from sample accession ERS633620 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633620" refname="UOS_IPD_324-sc-2201450" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633620</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_324-sc-2201450</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053699</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#9" center_name="The Wellcome Trust Sanger Institute" accession="ERX964357">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964357</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053616, constructed from sample accession ERS633621 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633621" refname="UOS_IPD_325-sc-2201451" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633621</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_325-sc-2201451</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053616</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#10" center_name="The Wellcome Trust Sanger Institute" accession="ERX964358">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964358</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053628, constructed from sample accession ERS633622 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633622" refname="UOS_IPD_326-sc-2201452" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633622</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_326-sc-2201452</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053628</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#11" center_name="The Wellcome Trust Sanger Institute" accession="ERX964359">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964359</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053640, constructed from sample accession ERS633623 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633623" refname="UOS_IPD_327-sc-2201453" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633623</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_327-sc-2201453</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053640</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#12" center_name="The Wellcome Trust Sanger Institute" accession="ERX964360">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964360</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053652, constructed from sample accession ERS633624 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633624" refname="UOS_IPD_328-sc-2201454" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633624</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_328-sc-2201454</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053652</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#13" center_name="The Wellcome Trust Sanger Institute" accession="ERX964361">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964361</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053664, constructed from sample accession ERS633625 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633625" refname="UOS_IPD_329-sc-2201455" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633625</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_329-sc-2201455</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053664</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#14" center_name="The Wellcome Trust Sanger Institute" accession="ERX964362">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964362</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053676, constructed from sample accession ERS633626 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633626" refname="UOS_IPD_331-sc-2201456" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633626</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_331-sc-2201456</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053676</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#15" center_name="The Wellcome Trust Sanger Institute" accession="ERX964363">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964363</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053688, constructed from sample accession ERS633627 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633627" refname="UOS_IPD_333-sc-2201458" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633627</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_333-sc-2201458</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053688</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#16" center_name="The Wellcome Trust Sanger Institute" accession="ERX964364">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964364</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053700, constructed from sample accession ERS633628 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633628" refname="UOS_IPD_334-sc-2201459" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633628</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_334-sc-2201459</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053700</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#17" center_name="The Wellcome Trust Sanger Institute" accession="ERX964365">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964365</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053617, constructed from sample accession ERS633629 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633629" refname="UOS_IPD_335-sc-2201460" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633629</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_335-sc-2201460</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053617</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#18" center_name="The Wellcome Trust Sanger Institute" accession="ERX964366">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964366</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053629, constructed from sample accession ERS633630 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633630" refname="UOS_IPD_336-sc-2201461" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633630</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_336-sc-2201461</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053629</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#19" center_name="The Wellcome Trust Sanger Institute" accession="ERX964367">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964367</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053641, constructed from sample accession ERS633631 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633631" refname="UOS_IPD_337-sc-2201462" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633631</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_337-sc-2201462</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053641</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#20" center_name="The Wellcome Trust Sanger Institute" accession="ERX964368">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964368</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053653, constructed from sample accession ERS633632 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633632" refname="UOS_IPD_338-sc-2201463" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633632</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_338-sc-2201463</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053653</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#21" center_name="The Wellcome Trust Sanger Institute" accession="ERX964369">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964369</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053665, constructed from sample accession ERS633633 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633633" refname="UOS_IPD_339-sc-2201464" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633633</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_339-sc-2201464</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053665</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#22" center_name="The Wellcome Trust Sanger Institute" accession="ERX964370">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964370</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053677, constructed from sample accession ERS633634 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633634" refname="UOS_IPD_340-sc-2201465" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633634</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_340-sc-2201465</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053677</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#23" center_name="The Wellcome Trust Sanger Institute" accession="ERX964371">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964371</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053689, constructed from sample accession ERS633635 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633635" refname="UOS_IPD_341-sc-2201466" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633635</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_341-sc-2201466</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053689</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#24" center_name="The Wellcome Trust Sanger Institute" accession="ERX964372">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964372</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053701, constructed from sample accession ERS633636 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633636" refname="UOS_IPD_342-sc-2201467" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633636</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_342-sc-2201467</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053701</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#25" center_name="The Wellcome Trust Sanger Institute" accession="ERX964373">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964373</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053618, constructed from sample accession ERS633637 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633637" refname="UOS_IPD_344-sc-2201468" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633637</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_344-sc-2201468</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053618</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#26" center_name="The Wellcome Trust Sanger Institute" accession="ERX964374">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964374</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053630, constructed from sample accession ERS633638 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633638" refname="UOS_IPD_345-sc-2201469" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633638</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_345-sc-2201469</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053630</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#27" center_name="The Wellcome Trust Sanger Institute" accession="ERX964375">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964375</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053642, constructed from sample accession ERS633639 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633639" refname="UOS_IPD_349-sc-2201470" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633639</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_349-sc-2201470</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053642</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#28" center_name="The Wellcome Trust Sanger Institute" accession="ERX964376">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964376</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053654, constructed from sample accession ERS633640 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633640" refname="UOS_IPD_350-sc-2201471" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633640</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_350-sc-2201471</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053654</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#29" center_name="The Wellcome Trust Sanger Institute" accession="ERX964377">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964377</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053666, constructed from sample accession ERS633641 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633641" refname="UOS_IPD_351-sc-2201472" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633641</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_351-sc-2201472</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053666</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#30" center_name="The Wellcome Trust Sanger Institute" accession="ERX964378">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964378</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053678, constructed from sample accession ERS633642 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633642" refname="UOS_IPD_352-sc-2201473" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633642</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_352-sc-2201473</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053678</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX964379">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964379</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053690, constructed from sample accession ERS633643 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633643" refname="UOS_IPD_353-sc-2201474" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633643</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_353-sc-2201474</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053690</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX964380">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964380</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053702, constructed from sample accession ERS633644 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633644" refname="UOS_IPD_354-sc-2201475" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633644</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_354-sc-2201475</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053702</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX964381">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964381</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053619, constructed from sample accession ERS633645 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633645" refname="UOS_IPD_356-sc-2201476" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633645</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_356-sc-2201476</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053619</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX964382">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964382</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053631, constructed from sample accession ERS633646 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633646" refname="UOS_IPD_357-sc-2201477" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633646</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_357-sc-2201477</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053631</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX964383">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964383</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053643, constructed from sample accession ERS633647 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633647" refname="UOS_IPD_358-sc-2201478" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633647</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_358-sc-2201478</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053643</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX964384">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964384</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053655, constructed from sample accession ERS633648 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633648" refname="UOS_IPD_359-sc-2201479" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633648</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_359-sc-2201479</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053655</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX964385">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964385</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053667, constructed from sample accession ERS633649 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633649" refname="UOS_IPD_362-sc-2201480" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633649</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_362-sc-2201480</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053667</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX964386">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964386</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053679, constructed from sample accession ERS633650 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633650" refname="UOS_IPD_363-sc-2201481" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633650</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_363-sc-2201481</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053679</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#39" center_name="The Wellcome Trust Sanger Institute" accession="ERX964387">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964387</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#39</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053691, constructed from sample accession ERS633651 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633651" refname="UOS_IPD_364-sc-2201482" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633651</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_364-sc-2201482</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053691</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#40" center_name="The Wellcome Trust Sanger Institute" accession="ERX964388">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964388</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#40</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053703, constructed from sample accession ERS633652 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633652" refname="UOS_IPD_365-sc-2201483" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633652</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_365-sc-2201483</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053703</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#41" center_name="The Wellcome Trust Sanger Institute" accession="ERX964389">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964389</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#41</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053620, constructed from sample accession ERS633653 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633653" refname="UOS_IPD_366-sc-2201484" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633653</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_366-sc-2201484</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053620</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#42" center_name="The Wellcome Trust Sanger Institute" accession="ERX964390">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964390</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#42</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053632, constructed from sample accession ERS633654 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633654" refname="UOS_IPD_367-sc-2201485" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633654</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_367-sc-2201485</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053632</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#43" center_name="The Wellcome Trust Sanger Institute" accession="ERX964391">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964391</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#43</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053644, constructed from sample accession ERS633655 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633655" refname="UOS_IPD_375-sc-2201486" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633655</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_375-sc-2201486</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053644</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#44" center_name="The Wellcome Trust Sanger Institute" accession="ERX964392">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964392</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#44</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053656, constructed from sample accession ERS633656 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633656" refname="UOS_IPD_382-sc-2201487" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633656</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_382-sc-2201487</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053656</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#45" center_name="The Wellcome Trust Sanger Institute" accession="ERX964393">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964393</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#45</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053668, constructed from sample accession ERS633657 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633657" refname="UOS_IPD_388-sc-2201488" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633657</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_388-sc-2201488</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053668</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#46" center_name="The Wellcome Trust Sanger Institute" accession="ERX964394">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964394</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#46</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053680, constructed from sample accession ERS633659 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633659" refname="UOS_IPD_402-sc-2201490" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633659</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_402-sc-2201490</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053680</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#47" center_name="The Wellcome Trust Sanger Institute" accession="ERX964395">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964395</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#47</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053692, constructed from sample accession ERS633660 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633660" refname="UOS_IPD_404-sc-2201491" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633660</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_404-sc-2201491</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053692</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#48" center_name="The Wellcome Trust Sanger Institute" accession="ERX964396">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964396</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#48</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053704, constructed from sample accession ERS633661 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633661" refname="UOS_IPD_406-sc-2201492" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633661</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_406-sc-2201492</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053704</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#49" center_name="The Wellcome Trust Sanger Institute" accession="ERX964397">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964397</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#49</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053621, constructed from sample accession ERS633662 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633662" refname="UOS_IPD_408-sc-2201493" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633662</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_408-sc-2201493</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053621</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#50" center_name="The Wellcome Trust Sanger Institute" accession="ERX964398">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964398</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#50</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053633, constructed from sample accession ERS633663 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633663" refname="UOS_IPD_409-sc-2201494" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633663</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_409-sc-2201494</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053633</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#51" center_name="The Wellcome Trust Sanger Institute" accession="ERX964399">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964399</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#51</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053645, constructed from sample accession ERS633664 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633664" refname="UOS_IPD_410-sc-2201495" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633664</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_410-sc-2201495</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053645</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#52" center_name="The Wellcome Trust Sanger Institute" accession="ERX964400">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964400</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#52</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053657, constructed from sample accession ERS633665 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633665" refname="UOS_IPD_411-sc-2201497" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633665</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_411-sc-2201497</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053657</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#53" center_name="The Wellcome Trust Sanger Institute" accession="ERX964401">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964401</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#53</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053669, constructed from sample accession ERS633666 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633666" refname="UOS_IPD_412-sc-2201498" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633666</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_412-sc-2201498</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053669</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#54" center_name="The Wellcome Trust Sanger Institute" accession="ERX964402">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964402</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#54</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053681, constructed from sample accession ERS633667 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633667" refname="UOS_IPD_413-sc-2201499" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633667</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_413-sc-2201499</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053681</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#55" center_name="The Wellcome Trust Sanger Institute" accession="ERX964403">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964403</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#55</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053693, constructed from sample accession ERS633668 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633668" refname="UOS_IPD_414-sc-2201500" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633668</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_414-sc-2201500</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053693</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#56" center_name="The Wellcome Trust Sanger Institute" accession="ERX964404">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964404</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#56</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053705, constructed from sample accession ERS633669 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633669" refname="UOS_IPD_416-sc-2201501" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633669</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_416-sc-2201501</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053705</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#57" center_name="The Wellcome Trust Sanger Institute" accession="ERX964405">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964405</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#57</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053622, constructed from sample accession ERS633670 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633670" refname="UOS_IPD_423-sc-2201502" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633670</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_423-sc-2201502</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053622</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#58" center_name="The Wellcome Trust Sanger Institute" accession="ERX964406">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964406</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#58</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053634, constructed from sample accession ERS633671 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633671" refname="UOS_IPD_424-sc-2201503" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633671</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_424-sc-2201503</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053634</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#59" center_name="The Wellcome Trust Sanger Institute" accession="ERX964407">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964407</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#59</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053646, constructed from sample accession ERS633672 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633672" refname="UOS_IPD_425-sc-2201504" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633672</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_425-sc-2201504</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053646</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#60" center_name="The Wellcome Trust Sanger Institute" accession="ERX964408">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964408</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#60</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#60</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053658, constructed from sample accession ERS633673 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633673" refname="UOS_IPD_427-sc-2201505" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633673</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_427-sc-2201505</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053658</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#61" center_name="The Wellcome Trust Sanger Institute" accession="ERX964409">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964409</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#61</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053670, constructed from sample accession ERS633674 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633674" refname="UOS_IPD_429-sc-2201506" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633674</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_429-sc-2201506</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053670</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#62" center_name="The Wellcome Trust Sanger Institute" accession="ERX964410">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964410</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#62</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053682, constructed from sample accession ERS633675 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633675" refname="UOS_IPD_430-sc-2201507" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633675</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_430-sc-2201507</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053682</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#63" center_name="The Wellcome Trust Sanger Institute" accession="ERX964411">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964411</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#63</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#63</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053694, constructed from sample accession ERS633676 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633676" refname="UOS_IPD_431-sc-2201508" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633676</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_431-sc-2201508</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053694</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#64" center_name="The Wellcome Trust Sanger Institute" accession="ERX964412">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964412</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#64</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#64</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053706, constructed from sample accession ERS633677 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633677" refname="UOS_IPD_432-sc-2201509" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633677</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_432-sc-2201509</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053706</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#65" center_name="The Wellcome Trust Sanger Institute" accession="ERX964413">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964413</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#65</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#65</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053623, constructed from sample accession ERS633678 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633678" refname="UOS_IPD_433-sc-2201510" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633678</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_433-sc-2201510</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053623</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#66" center_name="The Wellcome Trust Sanger Institute" accession="ERX964414">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964414</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#66</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#66</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053635, constructed from sample accession ERS633679 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633679" refname="UOS_IPD_435-sc-2201511" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633679</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_435-sc-2201511</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053635</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#67" center_name="The Wellcome Trust Sanger Institute" accession="ERX964415">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964415</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#67</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053647, constructed from sample accession ERS633680 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633680" refname="UOS_IPD_436-sc-2201512" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633680</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_436-sc-2201512</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053647</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#68" center_name="The Wellcome Trust Sanger Institute" accession="ERX964416">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964416</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#68</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053659, constructed from sample accession ERS633682 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633682" refname="UOS_IPD_437-sc-2201513" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633682</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_437-sc-2201513</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053659</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#69" center_name="The Wellcome Trust Sanger Institute" accession="ERX964417">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964417</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#69</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#69</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053671, constructed from sample accession ERS633683 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633683" refname="UOS_IPD_441-sc-2201514" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633683</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_441-sc-2201514</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053671</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#70" center_name="The Wellcome Trust Sanger Institute" accession="ERX964418">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964418</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#70</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#70</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053683, constructed from sample accession ERS633684 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633684" refname="UOS_IPD_442-sc-2201515" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633684</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_442-sc-2201515</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053683</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#71" center_name="The Wellcome Trust Sanger Institute" accession="ERX964419">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964419</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#71</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#71</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053695, constructed from sample accession ERS633685 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence GTGTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633685" refname="UOS_IPD_443-sc-2201516" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633685</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_443-sc-2201516</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053695</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#72" center_name="The Wellcome Trust Sanger Institute" accession="ERX964420">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964420</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#72</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#72</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053707, constructed from sample accession ERS633686 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence GACGGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633686" refname="UOS_IPD_444-sc-2201517" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633686</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_444-sc-2201517</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053707</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#73" center_name="The Wellcome Trust Sanger Institute" accession="ERX964421">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964421</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#73</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#73</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053624, constructed from sample accession ERS633687 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633687" refname="UOS_IPD_445-sc-2201518" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633687</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_445-sc-2201518</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053624</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#74" center_name="The Wellcome Trust Sanger Institute" accession="ERX964422">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964422</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#74</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053636, constructed from sample accession ERS633688 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633688" refname="UOS_IPD_446-sc-2201519" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633688</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_446-sc-2201519</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053636</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#75" center_name="The Wellcome Trust Sanger Institute" accession="ERX964423">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964423</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#75</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053648, constructed from sample accession ERS633689 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence GAATCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633689" refname="UOS_IPD_447-sc-2201520" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633689</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_447-sc-2201520</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053648</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#76" center_name="The Wellcome Trust Sanger Institute" accession="ERX964424">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964424</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#76</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053660, constructed from sample accession ERS633690 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633690" refname="UOS_IPD_448-sc-2201521" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633690</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_448-sc-2201521</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053660</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#77" center_name="The Wellcome Trust Sanger Institute" accession="ERX964425">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964425</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#77</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053672, constructed from sample accession ERS633691 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633691" refname="UOS_IPD_450-sc-2201522" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633691</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_450-sc-2201522</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053672</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#78" center_name="The Wellcome Trust Sanger Institute" accession="ERX964426">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964426</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#78</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#78</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053684, constructed from sample accession ERS633692 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633692" refname="UOS_IPD_451-sc-2201523" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633692</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_451-sc-2201523</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053684</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15682_8#79" center_name="The Wellcome Trust Sanger Institute" accession="ERX964427">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964427</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15682_8#79</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15682_8#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005855" refname="Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005855</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Identifying_pneumococcal_genetic_determinants_for_progression_from_colonisation_to_serious_disease-sc-3063</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13053696, constructed from sample accession ERS633693 for study accession ERP005855.  This is part of an Illumina multiplexed sequencing run (15682_8).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS633693" refname="UOS_IPD_454-sc-2201524" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS633693</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">UOS_IPD_454-sc-2201524</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13053696</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_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>
