<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX9743641" alias="F7T60C">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX9743641</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB8808968">F7T60C</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>F7 60 replicate C</TITLE>
    <STUDY_REF accession="SRP299501">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP299501</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA688285</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>A total of 288 ng of DNA was used for the production of paired-end libraries and for sequencing the V4V5 hypervariable regions of the bacterial 16S rRNA gene by using as primers 515F forward primer (5-GTGCCAGCMGCCG CGGTAA-3) and 907R reverse primer (5-CCGTCAATTCCTTTGAGTTT-3).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS7931510">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS7931510</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|237671@studenti.unimore.it">F7T60C</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>F7T60C</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
