<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX12842247" alias="1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12842247</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10589795">1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>WashedPlates</TITLE>
    <STUDY_REF accession="SRP343820">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP343820</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB10589795">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total DNA was isolated using QIAamp Fast DNA Stool Mini Kit (Qiagen, Hilden, Germany). PCR was performed using Q5 DNA polymerase (New England Biolabs) with a primer set selected to amplify V3-V4 region of 16S rRNA gene. Sequencing was performed on an Illumina MiSeq (2 x 300 bp), following the method detailed by Fadrosh et al. 2014.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10786207">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10786207</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|haovan1">WashedPlates</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
