<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX23836629" alias="C1_1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23836629</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14284623">C1_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Metagenome-assembled genomes</TITLE>
    <STUDY_REF accession="SRP493354">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493354</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14284623">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Firstly, the qualified DNA samples underwent enzymatic digestion, random fragmentation, end repair, addition of A-tail, addition of sequencing adapters, purification, PCR amplification, and other steps to complete the entire library preparation. Then, the constructed library was sequenced using Illumina HiSeq PE150, and the library with the best sequencing quality was selected for assembly.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20657551">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20657551</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|wenqcom@orcid">C1_1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>C1_1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 1500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
