<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="ERX7849214" alias="SC_EXP_30075_1#24" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX7849214</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30075_1#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP107671">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP107671</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB25725</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539245N:H1, constructed from sample accession ERS3359793 for study accession ERP107671.  This is part of an Illumina multiplexed sequencing run (30075_1).  This submission includes reads tagged with the sequence GGGTGTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3359793">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3359793</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5557755</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539245N:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX7849215" alias="SC_EXP_30075_2#62" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX7849215</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30075_2#62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP107671">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP107671</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB25725</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539249R:E3, constructed from sample accession ERS3360072 for study accession ERP107671.  This is part of an Illumina multiplexed sequencing run (30075_2).  This submission includes reads tagged with the sequence GCCATTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3360072">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3360072</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5558035</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539249R:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX7849216" alias="SC_EXP_30075_2#203" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX7849216</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30075_2#203</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP107671">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP107671</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB25725</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536956C:B10, constructed from sample accession ERS3360018 for study accession ERP107671.  This is part of an Illumina multiplexed sequencing run (30075_2).  This submission includes reads tagged with the sequence GGGTGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3360018">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3360018</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5557981</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536956C:B10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
