<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX5250031" alias="383">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5250031</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5040577">383</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Draft WGS of strain 383</TITLE>
    <STUDY_REF accession="SRP179443">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP179443</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA495731</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>genomic DNA was extracted with NZY Microbial gDNA (NZYTech, Portugal). Libraries were prepared using the Nextera XT library prep workflow (Illumina), and 2  150-nucleotide (nt) paired-end reads were generated on an Illumina MiSeq instrument. Quality trimming was executed using the sliding-window operation in TrimGalore  with default parameters. The final assembly was performed using the SPAdes assembler (version 3.50) using kmers of 33, 55 and 77 nt. The assembly was subjected to binning with metabat and quality check was performed on the final resulting file with checkM.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4251985">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4251985</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10231585</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>383</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
