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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX5415510" alias="198-5">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5415510</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5220772">198-5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>WGS of Pseudomonas</TITLE>
    <STUDY_REF accession="SRP186693">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP186693</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA523885</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA samples were sheared into 400-500 bp fragments using a Covaris M230 Focused-ultrasonicatorTM (ThermoFisher Scientific, Waltham, Massachusetts, USA) according to manufacturers protocol. Illumina sequencing libraries were prepared from the sheared fragm</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4396399">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4396399</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10992020</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>198-5</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>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5415511" alias="162-2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5415511</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5220772">162-2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>WGS of Pseudomonas</TITLE>
    <STUDY_REF accession="SRP186693">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP186693</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA523885</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA samples were sheared into 400-500 bp fragments using a Covaris M228 Focused-ultrasonicatorTM (ThermoFisher Scientific, Waltham, Massachusetts, USA) according to manufacturers protocol. Illumina sequencing libraries were prepared from the sheared fragm</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4396400">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4396400</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10992018</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>162-2</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>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5415512" alias="191-2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5415512</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5220772">191-2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>WGS of Pseudomonas</TITLE>
    <STUDY_REF accession="SRP186693">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP186693</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA523885</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA samples were sheared into 400-500 bp fragments using a Covaris M229 Focused-ultrasonicatorTM (ThermoFisher Scientific, Waltham, Massachusetts, USA) according to manufacturers protocol. Illumina sequencing libraries were prepared from the sheared fragm</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4396401">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4396401</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10992019</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>191-2</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>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5415513" alias="136-3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5415513</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5220772">136-3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>WGS of Pseudomonas</TITLE>
    <STUDY_REF accession="SRP186693">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP186693</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA523885</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA samples were sheared into 400-500 bp fragments using a Covaris M224 Focused-ultrasonicatorTM (ThermoFisher Scientific, Waltham, Massachusetts, USA) according to manufacturers protocol. Illumina sequencing libraries were prepared from the sheared fragm</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4396402">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4396402</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10992014</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>136-3</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>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5415514" alias="149-1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5415514</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5220772">149-1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>WGS of Pseudomonas</TITLE>
    <STUDY_REF accession="SRP186693">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP186693</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA523885</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA samples were sheared into 400-500 bp fragments using a Covaris M225 Focused-ultrasonicatorTM (ThermoFisher Scientific, Waltham, Massachusetts, USA) according to manufacturers protocol. Illumina sequencing libraries were prepared from the sheared fragm</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4396403">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4396403</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10992015</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>149-1</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>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5415515" alias="149-2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5415515</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5220772">149-2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>WGS of Pseudomonas</TITLE>
    <STUDY_REF accession="SRP186693">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP186693</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA523885</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA samples were sheared into 400-500 bp fragments using a Covaris M226 Focused-ultrasonicatorTM (ThermoFisher Scientific, Waltham, Massachusetts, USA) according to manufacturers protocol. Illumina sequencing libraries were prepared from the sheared fragm</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4396404">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4396404</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10992016</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>149-2</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>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5415516" alias="161-1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5415516</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5220772">161-1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>WGS of Pseudomonas</TITLE>
    <STUDY_REF accession="SRP186693">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP186693</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA523885</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA samples were sheared into 400-500 bp fragments using a Covaris M227 Focused-ultrasonicatorTM (ThermoFisher Scientific, Waltham, Massachusetts, USA) according to manufacturers protocol. Illumina sequencing libraries were prepared from the sheared fragm</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4396405">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4396405</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10992017</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>161-1</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>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5415517" alias="75-3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5415517</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5220772">75-3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>WGS of Pseudomonas</TITLE>
    <STUDY_REF accession="SRP186693">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP186693</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA523885</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA samples were sheared into 400-500 bp fragments using a Covaris M220 Focused-ultrasonicatorTM (ThermoFisher Scientific, Waltham, Massachusetts, USA) according to manufacturers protocol. Illumina sequencing libraries were prepared from the sheared fragments using the NEXTflex Rapid DNA-Seq Kit (Bioo Scientific, Austin, TX, USA). Briefly, 5 prime ends were first end-repaired and phosphorylated. Next, the 3 ends were A-tailed and ligated to sequencing adapters. The third step is to enrich the adapters-ligated products using PCR. The prepared libraries were then used for paired-end Illumina sequencing (2  150 bp) on an Illumina HiSeq X Ten machine (Illumina, San Diego, CA, USA).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4396406">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4396406</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10992010</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>75-3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5415518" alias="93-4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5415518</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5220772">93-4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>WGS of Pseudomonas</TITLE>
    <STUDY_REF accession="SRP186693">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP186693</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA523885</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA samples were sheared into 400-500 bp fragments using a Covaris M221 Focused-ultrasonicatorTM (ThermoFisher Scientific, Waltham, Massachusetts, USA) according to manufacturers protocol. Illumina sequencing libraries were prepared from the sheared fragm</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4396407">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4396407</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10992011</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>93-4</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>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5415519" alias="112-5">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5415519</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5220772">112-5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>WGS of Pseudomonas</TITLE>
    <STUDY_REF accession="SRP186693">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP186693</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA523885</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA samples were sheared into 400-500 bp fragments using a Covaris M222 Focused-ultrasonicatorTM (ThermoFisher Scientific, Waltham, Massachusetts, USA) according to manufacturers protocol. Illumina sequencing libraries were prepared from the sheared fragm</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4396408">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4396408</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10992012</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>112-5</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>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5415520" alias="131-1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5415520</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5220772">131-1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>WGS of Pseudomonas</TITLE>
    <STUDY_REF accession="SRP186693">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP186693</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA523885</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA samples were sheared into 400-500 bp fragments using a Covaris M223 Focused-ultrasonicatorTM (ThermoFisher Scientific, Waltham, Massachusetts, USA) according to manufacturers protocol. Illumina sequencing libraries were prepared from the sheared fragm</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4396409">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4396409</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10992013</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>131-1</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>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
