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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="SC_EXP_14992_1#93" center_name="The Wellcome Trust Sanger Institute" accession="ERX980328">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX980328</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14992_1#93</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14992_1#93</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005466" refname="ICONIC-sc-3034" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005466</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">ICONIC-sc-3034</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12178429, constructed from sample accession ERS569015 for study accession ERP005466.  This is part of an Illumina multiplexed sequencing run (14992_1).  This submission includes reads tagged with the sequence GCACTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS569015" refname="6114_S1_1RICONIC_Flu-sc-2152243" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS569015</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">6114_S1_1RICONIC_Flu-sc-2152243</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12178429</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="350"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14992_1#94" center_name="The Wellcome Trust Sanger Institute" accession="ERX980329">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX980329</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14992_1#94</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14992_1#94</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005466" refname="ICONIC-sc-3034" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005466</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">ICONIC-sc-3034</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12178430, constructed from sample accession ERS569016 for study accession ERP005466.  This is part of an Illumina multiplexed sequencing run (14992_1).  This submission includes reads tagged with the sequence GCTAACTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS569016" refname="6115_S1_1RICONIC_Flu-sc-2152244" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS569016</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">6115_S1_1RICONIC_Flu-sc-2152244</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12178430</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="350"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14992_1#95" center_name="The Wellcome Trust Sanger Institute" accession="ERX980330">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX980330</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14992_1#95</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14992_1#95</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005466" refname="ICONIC-sc-3034" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005466</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">ICONIC-sc-3034</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12178431, constructed from sample accession ERS569017 for study accession ERP005466.  This is part of an Illumina multiplexed sequencing run (14992_1).  This submission includes reads tagged with the sequence GATTCATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS569017" refname="6118_S1_1RICONIC_Flu-sc-2152245" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS569017</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">6118_S1_1RICONIC_Flu-sc-2152245</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12178431</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="350"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14992_1#96" center_name="The Wellcome Trust Sanger Institute" accession="ERX980331">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX980331</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14992_1#96</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14992_1#96</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP005466" refname="ICONIC-sc-3034" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005466</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">ICONIC-sc-3034</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 12178432, constructed from sample accession ERS569018 for study accession ERP005466.  This is part of an Illumina multiplexed sequencing run (14992_1).  This submission includes reads tagged with the sequence GTCTTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS569018" refname="6120_S1_1RICONIC_Flu-sc-2152246" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS569018</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">6120_S1_1RICONIC_Flu-sc-2152246</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12178432</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="350"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
