<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX18026785" alias="HJNKWDSX2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18026785</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12153220">HJNKWDSX2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DH348</TITLE>
    <STUDY_REF accession="SRP404581">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP404581</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12153220">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR-free libraries were produced from the DNA samples with &gt;600bp insert sizes (gel size-selection) and sequenced on Illumina NovaSeq 6000 S4 flowcells to produce 150bp paired-end reads</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15533963">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15533963</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|surbhi.grewal@nottingham.ac.uk">IL DH348</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>HJNKWDSX2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18026786" alias="HHHK5DSX2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18026786</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12153220">HHHK5DSX2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>T4B4S</TITLE>
    <STUDY_REF accession="SRP404581">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP404581</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12153220">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR-free libraries were produced from the DNA samples with &gt;600bp insert sizes (gel size-selection) and sequenced on Illumina NovaSeq 6000 S4 flowcells to produce 150bp paired-end reads</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15533964">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15533964</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|surbhi.grewal@nottingham.ac.uk">IL T4B4S</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>HHHK5DSX2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
