<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="ERX5014660" alias="SC_EXP_15169_6#53" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX5014660</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_15169_6#53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115951">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115951</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33181</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN380891O:E7, constructed from sample accession ERS5634726 for study accession ERP115951.  This is part of an Illumina multiplexed sequencing run (15169_6).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS5634726">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS5634726</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7887490</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN380891O:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX5014661" alias="SC_EXP_15169_6#65" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX5014661</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_15169_6#65</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115951">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115951</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33181</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN380891O:A9, constructed from sample accession ERS5634727 for study accession ERP115951.  This is part of an Illumina multiplexed sequencing run (15169_6).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS5634727">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS5634727</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7887491</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN380891O:A9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="250"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
