<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="SC_EXP_14992_1#91" center_name="The Wellcome Trust Sanger Institute" accession="ERX964122">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964122</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14992_1#91</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14992_1#91</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 12178427, constructed from sample accession ERS569013 for study accession ERP005466.  This is part of an Illumina multiplexed sequencing run (14992_1).  This submission includes reads tagged with the sequence GACCTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS569013" refname="6110_S1_1RICONIC_Flu-sc-2152241" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS569013</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">6110_S1_1RICONIC_Flu-sc-2152241</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12178427</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#1" center_name="The Wellcome Trust Sanger Institute" accession="ERX964116">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964116</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14992_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14992_1#1</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 12178433, constructed from sample accession ERS569019 for study accession ERP005466.  This is part of an Illumina multiplexed sequencing run (14992_1).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS569019" refname="6124_S1_1RICONIC_Flu-sc-2152247" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS569019</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">6124_S1_1RICONIC_Flu-sc-2152247</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12178433</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#5" center_name="The Wellcome Trust Sanger Institute" accession="ERX964117">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964117</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14992_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14992_1#5</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 12178437, constructed from sample accession ERS569023 for study accession ERP005466.  This is part of an Illumina multiplexed sequencing run (14992_1).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS569023" refname="6174_S1_1RICONIC_Flu-sc-2152251" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS569023</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">6174_S1_1RICONIC_Flu-sc-2152251</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12178437</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#6" center_name="The Wellcome Trust Sanger Institute" accession="ERX964118">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964118</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14992_1#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14992_1#6</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 12178438, constructed from sample accession ERS569024 for study accession ERP005466.  This is part of an Illumina multiplexed sequencing run (14992_1).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS569024" refname="6180_S1_1RICONIC_Flu-sc-2152252" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS569024</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">6180_S1_1RICONIC_Flu-sc-2152252</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12178438</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#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX964119">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964119</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14992_1#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14992_1#8</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 12178440, constructed from sample accession ERS569026 for study accession ERP005466.  This is part of an Illumina multiplexed sequencing run (14992_1).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS569026" refname="6185_S1_1RICONIC_Flu-sc-2152254" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS569026</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">6185_S1_1RICONIC_Flu-sc-2152254</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12178440</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#87" center_name="The Wellcome Trust Sanger Institute" accession="ERX964120">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964120</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14992_1#87</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14992_1#87</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 12178423, constructed from sample accession ERS569009 for study accession ERP005466.  This is part of an Illumina multiplexed sequencing run (14992_1).  This submission includes reads tagged with the sequence GGATTAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS569009" refname="6101_S1_1RS1_1RICONIC_Flu-sc-2152237" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS569009</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">6101_S1_1RS1_1RICONIC_Flu-sc-2152237</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12178423</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#88" center_name="The Wellcome Trust Sanger Institute" accession="ERX964121">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX964121</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14992_1#88</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14992_1#88</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 12178424, constructed from sample accession ERS569010 for study accession ERP005466.  This is part of an Illumina multiplexed sequencing run (14992_1).  This submission includes reads tagged with the sequence GATAGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS569010" refname="6104_S1_1RICONIC_Flu-sc-2152238" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS569010</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">6104_S1_1RICONIC_Flu-sc-2152238</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12178424</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>
