<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX23203827" alias="SO_10792_4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23203827</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14144274">SO_10792_4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>S 4</TITLE>
    <STUDY_REF accession="SRP483483">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP483483</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1059795</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>50 ng of Qubit quantified DNA was enzymatically fragmented, end-repaired and A-tailed in a one-tube reaction using the FX Enzyme Mix provided. The end-repaired and adenylated fragments were subjected to adapter ligation, whereby index-incorporated Illumina adapter was ligated, to generate sequencing library. The library was subjected to 6 cycles of Indexing-PCR (Initial Denaturation at 98C for 2 min, cycling (98C for 20sec, 60C for 30sec, 72C for 30sec) and final extension at 72C for 1min) to enrich the adapter-tagged fragments. Finally, the amplified libraries were purified using Sera-MagTM Select beads followed by library quality control check.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20128149">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20128149</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN39327841</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SO_10792_4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
