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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="SC_EXP_15795_5#1" center_name="The Wellcome Trust Sanger Institute" accession="ERX984773">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX984773</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15795_5#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15795_5#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000767" refname="Investigating_the_global_genomic_diversity_of_the_L__donovani_complex-sc-2011-07-04T13:27:50Z-1890" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000767</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Investigating_the_global_genomic_diversity_of_the_L__donovani_complex-sc-2011-07-04T13:27:50Z-1890</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13074676, constructed from sample accession ERS631701 for study accession ERP000767.  This is part of an Illumina multiplexed sequencing run (15795_5).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS631701" refname="Linf_C40-sc-2200907" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631701</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">Linf_C40-sc-2200907</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13074676</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="392" NOMINAL_SDEV="119"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15795_5#2" center_name="The Wellcome Trust Sanger Institute" accession="ERX984774">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX984774</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15795_5#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15795_5#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000767" refname="Investigating_the_global_genomic_diversity_of_the_L__donovani_complex-sc-2011-07-04T13:27:50Z-1890" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000767</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Investigating_the_global_genomic_diversity_of_the_L__donovani_complex-sc-2011-07-04T13:27:50Z-1890</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13074677, constructed from sample accession ERS631702 for study accession ERP000767.  This is part of an Illumina multiplexed sequencing run (15795_5).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS631702" refname="Linf_C41-sc-2200908" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631702</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">Linf_C41-sc-2200908</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13074677</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="392" NOMINAL_SDEV="119"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15795_5#3" center_name="The Wellcome Trust Sanger Institute" accession="ERX984775">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX984775</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15795_5#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15795_5#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000767" refname="Investigating_the_global_genomic_diversity_of_the_L__donovani_complex-sc-2011-07-04T13:27:50Z-1890" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000767</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Investigating_the_global_genomic_diversity_of_the_L__donovani_complex-sc-2011-07-04T13:27:50Z-1890</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13074678, constructed from sample accession ERS631703 for study accession ERP000767.  This is part of an Illumina multiplexed sequencing run (15795_5).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS631703" refname="Linf_C42-sc-2200909" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631703</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">Linf_C42-sc-2200909</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13074678</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="392" NOMINAL_SDEV="119"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15795_5#4" center_name="The Wellcome Trust Sanger Institute" accession="ERX984776">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX984776</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15795_5#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15795_5#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000767" refname="Investigating_the_global_genomic_diversity_of_the_L__donovani_complex-sc-2011-07-04T13:27:50Z-1890" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000767</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Investigating_the_global_genomic_diversity_of_the_L__donovani_complex-sc-2011-07-04T13:27:50Z-1890</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13074679, constructed from sample accession ERS631704 for study accession ERP000767.  This is part of an Illumina multiplexed sequencing run (15795_5).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS631704" refname="Linf_C43-sc-2200910" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631704</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">Linf_C43-sc-2200910</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13074679</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="392" NOMINAL_SDEV="119"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15795_5#5" center_name="The Wellcome Trust Sanger Institute" accession="ERX984777">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX984777</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15795_5#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15795_5#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000767" refname="Investigating_the_global_genomic_diversity_of_the_L__donovani_complex-sc-2011-07-04T13:27:50Z-1890" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000767</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Investigating_the_global_genomic_diversity_of_the_L__donovani_complex-sc-2011-07-04T13:27:50Z-1890</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13074680, constructed from sample accession ERS631705 for study accession ERP000767.  This is part of an Illumina multiplexed sequencing run (15795_5).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS631705" refname="Linf_C46-sc-2200911" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631705</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">Linf_C46-sc-2200911</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13074680</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="392" NOMINAL_SDEV="119"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15795_5#6" center_name="The Wellcome Trust Sanger Institute" accession="ERX984778">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX984778</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15795_5#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15795_5#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000767" refname="Investigating_the_global_genomic_diversity_of_the_L__donovani_complex-sc-2011-07-04T13:27:50Z-1890" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000767</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Investigating_the_global_genomic_diversity_of_the_L__donovani_complex-sc-2011-07-04T13:27:50Z-1890</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13074681, constructed from sample accession ERS631706 for study accession ERP000767.  This is part of an Illumina multiplexed sequencing run (15795_5).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS631706" refname="Linf_C47-sc-2200912" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631706</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">Linf_C47-sc-2200912</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13074681</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="392" NOMINAL_SDEV="119"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15795_5#7" center_name="The Wellcome Trust Sanger Institute" accession="ERX984779">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX984779</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15795_5#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15795_5#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000767" refname="Investigating_the_global_genomic_diversity_of_the_L__donovani_complex-sc-2011-07-04T13:27:50Z-1890" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000767</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Investigating_the_global_genomic_diversity_of_the_L__donovani_complex-sc-2011-07-04T13:27:50Z-1890</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13074682, constructed from sample accession ERS631707 for study accession ERP000767.  This is part of an Illumina multiplexed sequencing run (15795_5).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS631707" refname="Linf_C48-sc-2200913" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631707</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">Linf_C48-sc-2200913</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13074682</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="392" NOMINAL_SDEV="119"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15795_5#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX984780">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX984780</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15795_5#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15795_5#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000767" refname="Investigating_the_global_genomic_diversity_of_the_L__donovani_complex-sc-2011-07-04T13:27:50Z-1890" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000767</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Investigating_the_global_genomic_diversity_of_the_L__donovani_complex-sc-2011-07-04T13:27:50Z-1890</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13074683, constructed from sample accession ERS631708 for study accession ERP000767.  This is part of an Illumina multiplexed sequencing run (15795_5).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS631708" refname="Linf_C49-sc-2200914" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631708</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">Linf_C49-sc-2200914</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13074683</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="392" NOMINAL_SDEV="119"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15795_5#9" center_name="The Wellcome Trust Sanger Institute" accession="ERX984781">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX984781</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15795_5#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15795_5#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000767" refname="Investigating_the_global_genomic_diversity_of_the_L__donovani_complex-sc-2011-07-04T13:27:50Z-1890" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000767</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Investigating_the_global_genomic_diversity_of_the_L__donovani_complex-sc-2011-07-04T13:27:50Z-1890</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13074684, constructed from sample accession ERS631709 for study accession ERP000767.  This is part of an Illumina multiplexed sequencing run (15795_5).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS631709" refname="Linf_C50-sc-2200915" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631709</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">Linf_C50-sc-2200915</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13074684</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="392" NOMINAL_SDEV="119"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15795_5#10" center_name="The Wellcome Trust Sanger Institute" accession="ERX984782">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX984782</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15795_5#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15795_5#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000767" refname="Investigating_the_global_genomic_diversity_of_the_L__donovani_complex-sc-2011-07-04T13:27:50Z-1890" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000767</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Investigating_the_global_genomic_diversity_of_the_L__donovani_complex-sc-2011-07-04T13:27:50Z-1890</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13074685, constructed from sample accession ERS631710 for study accession ERP000767.  This is part of an Illumina multiplexed sequencing run (15795_5).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS631710" refname="Linf_V1-sc-2200916" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631710</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">Linf_V1-sc-2200916</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13074685</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="392" NOMINAL_SDEV="119"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15795_5#11" center_name="The Wellcome Trust Sanger Institute" accession="ERX984783">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX984783</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15795_5#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15795_5#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000767" refname="Investigating_the_global_genomic_diversity_of_the_L__donovani_complex-sc-2011-07-04T13:27:50Z-1890" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000767</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Investigating_the_global_genomic_diversity_of_the_L__donovani_complex-sc-2011-07-04T13:27:50Z-1890</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13074686, constructed from sample accession ERS631711 for study accession ERP000767.  This is part of an Illumina multiplexed sequencing run (15795_5).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS631711" refname="Linf_V11-sc-2200917" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631711</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">Linf_V11-sc-2200917</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13074686</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="392" NOMINAL_SDEV="119"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15795_5#12" center_name="The Wellcome Trust Sanger Institute" accession="ERX984784">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX984784</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15795_5#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15795_5#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000767" refname="Investigating_the_global_genomic_diversity_of_the_L__donovani_complex-sc-2011-07-04T13:27:50Z-1890" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000767</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Investigating_the_global_genomic_diversity_of_the_L__donovani_complex-sc-2011-07-04T13:27:50Z-1890</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13074687, constructed from sample accession ERS631712 for study accession ERP000767.  This is part of an Illumina multiplexed sequencing run (15795_5).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS631712" refname="Linf_V13-sc-2200918" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631712</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">Linf_V13-sc-2200918</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13074687</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="392" NOMINAL_SDEV="119"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15795_5#13" center_name="The Wellcome Trust Sanger Institute" accession="ERX984785">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX984785</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15795_5#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15795_5#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000767" refname="Investigating_the_global_genomic_diversity_of_the_L__donovani_complex-sc-2011-07-04T13:27:50Z-1890" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000767</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Investigating_the_global_genomic_diversity_of_the_L__donovani_complex-sc-2011-07-04T13:27:50Z-1890</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13074688, constructed from sample accession ERS631713 for study accession ERP000767.  This is part of an Illumina multiplexed sequencing run (15795_5).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS631713" refname="Linf_V14-sc-2200919" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631713</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">Linf_V14-sc-2200919</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13074688</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="392" NOMINAL_SDEV="119"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_15795_5#14" center_name="The Wellcome Trust Sanger Institute" accession="ERX984786">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX984786</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_15795_5#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_15795_5#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000767" refname="Investigating_the_global_genomic_diversity_of_the_L__donovani_complex-sc-2011-07-04T13:27:50Z-1890" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000767</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Investigating_the_global_genomic_diversity_of_the_L__donovani_complex-sc-2011-07-04T13:27:50Z-1890</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13074689, constructed from sample accession ERS631714 for study accession ERP000767.  This is part of an Illumina multiplexed sequencing run (15795_5).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS631714" refname="Linf_V4-sc-2200920" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631714</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">Linf_V4-sc-2200920</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13074689</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="392" NOMINAL_SDEV="119"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
