<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX23390107" alias="ES114">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23390107</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14169596">ES114</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Whole genome sequencing of V. fischeri strain ES114</TITLE>
    <STUDY_REF accession="SRP485907">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP485907</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14169596">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA from V. fischeri strains was extracted using the Invitrogen PureLink Genomic DNA Mini Kit. DNA was sonicated to generate fragments of approximately 500 bp, and gDNA libraries were prepared using the NEBNext Ultra II DNA library prep kit for Illumina, which includes end-repair, adaptor ligation, and addition of index primers. Sequencing was performed by the University of Georgia Genomics and Bioinformatics Coreon an Illumina NextSeq500 instrument.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20250971">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20250971</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mcoppinger">ES114</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>ES114</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23390108" alias="RMJ13S1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23390108</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14169596">RMJ13S1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Whole genome sequencing of V. fischeri strain derived from ES114</TITLE>
    <STUDY_REF accession="SRP485907">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP485907</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14169596">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA from V. fischeri strains was extracted using the Invitrogen PureLink Genomic DNA Mini Kit. DNA was sonicated to generate fragments of approximately 500 bp, and gDNA libraries were prepared using the NEBNext Ultra II DNA library prep kit for Illumina, which includes end-repair, adaptor ligation, and addition of index primers. Sequencing was performed by the University of Georgia Genomics and Bioinformatics Coreon an Illumina NextSeq500 instrument.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20250970">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20250970</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mcoppinger">RMJ13S1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RMJ13S1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23390109" alias="RMJ13S2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23390109</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14169596">RMJ13S2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Whole genome sequencing of V. fischeri strain derived from ES114</TITLE>
    <STUDY_REF accession="SRP485907">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP485907</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14169596">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA from V. fischeri strains was extracted using the Invitrogen PureLink Genomic DNA Mini Kit. DNA was sonicated to generate fragments of approximately 500 bp, and gDNA libraries were prepared using the NEBNext Ultra II DNA library prep kit for Illumina, which includes end-repair, adaptor ligation, and addition of index primers. Sequencing was performed by the University of Georgia Genomics and Bioinformatics Coreon an Illumina NextSeq500 instrument.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20250978">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20250978</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mcoppinger">RMJ13S2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RMJ13S2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23390110" alias="RMJ13S3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23390110</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14169596">RMJ13S3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Whole genome sequencing of V. fischeri strain derived from ES114</TITLE>
    <STUDY_REF accession="SRP485907">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP485907</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14169596">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA from V. fischeri strains was extracted using the Invitrogen PureLink Genomic DNA Mini Kit. DNA was sonicated to generate fragments of approximately 500 bp, and gDNA libraries were prepared using the NEBNext Ultra II DNA library prep kit for Illumina, which includes end-repair, adaptor ligation, and addition of index primers. Sequencing was performed by the University of Georgia Genomics and Bioinformatics Coreon an Illumina NextSeq500 instrument.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20250968">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20250968</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mcoppinger">RMJ13S3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RMJ13S3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23390111" alias="RMJ13S3.1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23390111</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14169596">RMJ13S3.1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Whole genome sequencing of V. fischeri strain derived from ES114</TITLE>
    <STUDY_REF accession="SRP485907">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP485907</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14169596">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA from V. fischeri strains was extracted using the Invitrogen PureLink Genomic DNA Mini Kit. DNA was sonicated to generate fragments of approximately 500 bp, and gDNA libraries were prepared using the NEBNext Ultra II DNA library prep kit for Illumina, which includes end-repair, adaptor ligation, and addition of index primers. Sequencing was performed by the University of Georgia Genomics and Bioinformatics Coreon an Illumina NextSeq500 instrument.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20250969">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20250969</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mcoppinger">RMJ13S3.1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RMJ13S3.1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23390112" alias="RMJ13S4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23390112</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14169596">RMJ13S4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Whole genome sequencing of V. fischeri strain derived from ES114</TITLE>
    <STUDY_REF accession="SRP485907">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP485907</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14169596">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA from V. fischeri strains was extracted using the Invitrogen PureLink Genomic DNA Mini Kit. DNA was sonicated to generate fragments of approximately 500 bp, and gDNA libraries were prepared using the NEBNext Ultra II DNA library prep kit for Illumina, which includes end-repair, adaptor ligation, and addition of index primers. Sequencing was performed by the University of Georgia Genomics and Bioinformatics Coreon an Illumina NextSeq500 instrument.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20250972">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20250972</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mcoppinger">RMJ13S4</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RMJ13S4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23390113" alias="RMJ13S5">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23390113</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14169596">RMJ13S5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Whole genome sequencing of V. fischeri strain derived from ES114</TITLE>
    <STUDY_REF accession="SRP485907">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP485907</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14169596">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA from V. fischeri strains was extracted using the Invitrogen PureLink Genomic DNA Mini Kit. DNA was sonicated to generate fragments of approximately 500 bp, and gDNA libraries were prepared using the NEBNext Ultra II DNA library prep kit for Illumina, which includes end-repair, adaptor ligation, and addition of index primers. Sequencing was performed by the University of Georgia Genomics and Bioinformatics Coreon an Illumina NextSeq500 instrument.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20250973">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20250973</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mcoppinger">RMJ13S5</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RMJ13S5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23390114" alias="RMJ13S6">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23390114</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14169596">RMJ13S6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Whole genome sequencing of V. fischeri strain derived from ES114</TITLE>
    <STUDY_REF accession="SRP485907">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP485907</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14169596">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA from V. fischeri strains was extracted using the Invitrogen PureLink Genomic DNA Mini Kit. DNA was sonicated to generate fragments of approximately 500 bp, and gDNA libraries were prepared using the NEBNext Ultra II DNA library prep kit for Illumina, which includes end-repair, adaptor ligation, and addition of index primers. Sequencing was performed by the University of Georgia Genomics and Bioinformatics Coreon an Illumina NextSeq500 instrument.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20250974">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20250974</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mcoppinger">RMJ13S6</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RMJ13S6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23390115" alias="RMJ13S8">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23390115</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14169596">RMJ13S8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Whole genome sequencing of V. fischeri strain derived from ES114</TITLE>
    <STUDY_REF accession="SRP485907">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP485907</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14169596">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA from V. fischeri strains was extracted using the Invitrogen PureLink Genomic DNA Mini Kit. DNA was sonicated to generate fragments of approximately 500 bp, and gDNA libraries were prepared using the NEBNext Ultra II DNA library prep kit for Illumina, which includes end-repair, adaptor ligation, and addition of index primers. Sequencing was performed by the University of Georgia Genomics and Bioinformatics Coreon an Illumina NextSeq500 instrument.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20250975">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20250975</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mcoppinger">RMJ13S8</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RMJ13S8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23390116" alias="RMJ13S10">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23390116</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14169596">RMJ13S10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Whole genome sequencing of V. fischeri strain derived from ES114</TITLE>
    <STUDY_REF accession="SRP485907">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP485907</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14169596">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA from V. fischeri strains was extracted using the Invitrogen PureLink Genomic DNA Mini Kit. DNA was sonicated to generate fragments of approximately 500 bp, and gDNA libraries were prepared using the NEBNext Ultra II DNA library prep kit for Illumina, which includes end-repair, adaptor ligation, and addition of index primers. Sequencing was performed by the University of Georgia Genomics and Bioinformatics Coreon an Illumina NextSeq500 instrument.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20250976">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20250976</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mcoppinger">RMJ13S10</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RMJ13S10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
