<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX18325922" alias="HISEQ:581:HMGV7BCX3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18325922</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12302235">HISEQ:581:HMGV7BCX3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>WGS of Elizabethkingia anophelis: ML-44</TITLE>
    <STUDY_REF accession="SRP408881">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408881</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA783500</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>According to the manufacturers instructions, genomic DNA was extracted from overnight E. anophelis culture using the QIAamp DNA Kit (Qiagen, Dsseldorf, Germany). DNA concentration was estimated using the Qubit dsDNA BR Assay Kit (Fisher Scientific, Waltham, MA, USA) on a Qubit 3.0 fluorometer (Fisher Scientific). Obtained DNA sample was sequenced using an Illumina HiSeq 1500 (Illumina, San Diego, CA, USA) by 150-bp paired-end reads.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15815281">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15815281</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN23435286</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>HISEQ:581:HMGV7BCX3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 1500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
