<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX5282364" alias="Uhlin_IHE3034R2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5282364</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5077577">Uhlin_IHE3034R2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>IHE3034F Chromosome</TITLE>
    <STUDY_REF accession="SRP181575">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP181575</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5077577">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We used Escherichia coli IHE3034 as our reference gnome, which was downloaded from ncbi ftp (ftp://ftp.ncbi.nlm.nih.gov/genomes/all/GCF/000/025/745/GCF_000025745.1_ASM2574v1). The reads were directly mapped to the reference genome by using BWA mem (version: 0.7.17) with the default parameters. The variants were called by using GATK HaplotypeCaller (version 4.0.2.1) (-stand-call-conf 30 -ploidy 1, other parameters are default). Filtering for low quality calls was done with GATK VariantFiltration for SNPs and indels separately (SNPs filtering criteria: QD &lt; 2.0 || FS &gt; 60.0 || MQ &lt; 40.0; Indel filtering criteria: QD &lt; 2.0 || FS &gt; 200.0)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4282109">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4282109</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|nikolazlatkov@gmail.com">IHE3034F</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Uhlin_IHE3034R2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
