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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX15039211" alias="Yp_NM_WGS-20">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15039211</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB11337489">Yp_NM_WGS-20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq of Y. pestis: Isolated from Unknown host</TITLE>
    <STUDY_REF accession="SRP372682">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372682</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB11337489">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Genomes were fragmented using the Covaris M220 focused-ultrasonicator. DNA cleaning was done with DNA-Clean and Concentrator kit. Ends were repaired with NEBNext Ultra II End Repair/dA-Tailing module and adapters were ligated using NEBNext Ultra II Ligation Module. Size selection was done with solid-phase reversible immobilization (SPRI) beads followed by KAPA Library Amplification Kit.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS12785836">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12785836</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|bpickett044">2015023558-b</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Yp_NM_WGS-20</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 MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15039212" alias="Yp_NM_WGS-3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15039212</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB11337489">Yp_NM_WGS-3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq of Y. pestis: Isolated from Feline host</TITLE>
    <STUDY_REF accession="SRP372682">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372682</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB11337489">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomes were fragmented using the Covaris M220 focused-ultrasonicator. DNA cleaning was done with DNA-Clean and Concentrator kit. Ends were repaired with NEBNext Ultra II End Repair/dA-Tailing module and adapters were ligated using NEBNext Ultra II Ligation Module. Size selection was done with solid-phase reversible immobilization (SPRI) beads followed by KAPA Library Amplification Kit.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS12785840">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12785840</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|bpickett044">88-3385</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Yp_NM_WGS-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>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
