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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="ERX4492750" alias="SC_EXP_26987_6#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4492750</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26987_6#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26987_6#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 sequencing</TITLE>
    <STUDY_REF accession="ERP107342">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP107342</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB25429</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN540716P:C2, constructed from sample accession ERS2653352 for study accession ERP107342.  This is part of an Illumina multiplexed sequencing run (26987_6).  This submission includes reads tagged with the sequence GGCTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2653352">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2653352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4833479</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN540716P:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Small RNA (miRNA)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4492751" alias="SC_EXP_26987_8#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4492751</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26987_8#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26987_8#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 sequencing</TITLE>
    <STUDY_REF accession="ERP107342">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP107342</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB25429</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN540716P:D3, constructed from sample accession ERS2653361 for study accession ERP107342.  This is part of an Illumina multiplexed sequencing run (26987_8).  This submission includes reads tagged with the sequence ACTTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2653361">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2653361</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4833488</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN540716P:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Small RNA (miRNA)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4492752" alias="SC_EXP_27847_6#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4492752</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_27847_6#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_27847_6#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP107342">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP107342</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB25429</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN548878S:F10, constructed from sample accession SAMEA5574023 for study accession ERP107342.  This is part of an Illumina multiplexed sequencing run (27847_6).  This submission includes reads tagged with the sequence GACAACCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS5189247">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS5189247</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5574023</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN548878S:F10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="200"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA PolyA</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4492753" alias="SC_EXP_27847_7#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4492753</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_27847_7#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_27847_7#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP107342">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP107342</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB25429</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN548878S:G10, constructed from sample accession SAMEA5574022 for study accession ERP107342.  This is part of an Illumina multiplexed sequencing run (27847_7).  This submission includes reads tagged with the sequence GATACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS5189248">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS5189248</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5574022</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN548878S:G10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="200"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA PolyA</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4492754" alias="SC_EXP_27847_7#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4492754</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_27847_7#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_27847_7#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP107342">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP107342</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB25429</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN548878S:H10, constructed from sample accession SAMEA5574024 for study accession ERP107342.  This is part of an Illumina multiplexed sequencing run (27847_7).  This submission includes reads tagged with the sequence CTATGTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS5189251">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS5189251</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5574024</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN548878S:H10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="200"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA PolyA</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4492755" alias="SC_EXP_27847_7#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4492755</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_27847_7#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_27847_7#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP107342">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP107342</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB25429</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN548878S:A11, constructed from sample accession SAMEA5574018 for study accession ERP107342.  This is part of an Illumina multiplexed sequencing run (27847_7).  This submission includes reads tagged with the sequence TTGTGCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS5189254">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS5189254</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5574018</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN548878S:A11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="200"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA PolyA</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4492756" alias="SC_EXP_27847_7#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4492756</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_27847_7#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_27847_7#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP107342">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP107342</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB25429</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN548878S:B11, constructed from sample accession SAMEA5574016 for study accession ERP107342.  This is part of an Illumina multiplexed sequencing run (27847_7).  This submission includes reads tagged with the sequence AAAGGTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS5189252">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS5189252</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5574016</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN548878S:B11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="200"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA PolyA</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4492757" alias="SC_EXP_27847_8#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4492757</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_27847_8#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_27847_8#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP107342">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP107342</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB25429</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN548878S:C11, constructed from sample accession SAMEA5574014 for study accession ERP107342.  This is part of an Illumina multiplexed sequencing run (27847_8).  This submission includes reads tagged with the sequence GGTCACAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS5189249">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS5189249</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5574014</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN548878S:C11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="200"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA PolyA</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4492758" alias="SC_EXP_27847_8#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4492758</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_27847_8#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_27847_8#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP107342">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP107342</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB25429</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN548878S:D11, constructed from sample accession SAMEA5574025 for study accession ERP107342.  This is part of an Illumina multiplexed sequencing run (27847_8).  This submission includes reads tagged with the sequence CATTCTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS5189250">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS5189250</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5574025</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN548878S:D11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="200"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA PolyA</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4492759" alias="SC_EXP_27847_8#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4492759</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_27847_8#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_27847_8#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP107342">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP107342</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB25429</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN548878S:E11, constructed from sample accession SAMEA5574026 for study accession ERP107342.  This is part of an Illumina multiplexed sequencing run (27847_8).  This submission includes reads tagged with the sequence CTCGACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS5189253">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS5189253</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5574026</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN548878S:E11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="200"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA PolyA</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4492760" alias="SC_EXP_27847_8#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4492760</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_27847_8#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_27847_8#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP107342">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP107342</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB25429</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN548878S:F11, constructed from sample accession SAMEA5574017 for study accession ERP107342.  This is part of an Illumina multiplexed sequencing run (27847_8).  This submission includes reads tagged with the sequence AGTTGCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS5189255">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS5189255</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5574017</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN548878S:F11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="200"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA PolyA</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
