<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX24174295" alias="LJ_5069">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX24174295</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14362661">LJ_5069</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Lactobacillus jensenii UMB5069</TITLE>
    <STUDY_REF accession="SRP072679">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP072679</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA316969</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA was extracted from liquid culture using the Qiagen DNeasy Blood and Tissue Microbial Kit following the manufacturers protocol for Gram-positive bacteria. DNA was sent to SeqCoast Genomics LLC (Portsmouth, NH USA) for library preparation and sequencing. Samples were prepared for whole genome sequencing using an Illumina DNA Prep tagmentation kit and unique dual indexes. Sequencing was performed on the Illumina NextSeq2000 platform using a 300-cycle flow cell kit, producing 2x150bp paired reads. 1-2% PhiX control was spiked into the run to support optimal base calling. Read demultiplexing, read trimming, and run analytics were performed using DRAGEN v3.10.12.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20950248">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20950248</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40858149</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>LJ_5069</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>NextSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX24174296" alias="LJ_1855">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX24174296</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14362661">LJ_1855</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Lactobacillus jensenii UMB1855</TITLE>
    <STUDY_REF accession="SRP072679">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP072679</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA316969</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA was extracted from liquid culture using the Qiagen DNeasy Blood and Tissue Microbial Kit following the manufacturers protocol for Gram-positive bacteria. DNA was sent to SeqCoast Genomics LLC (Portsmouth, NH USA) for library preparation and sequencing. Samples were prepared for whole genome sequencing using an Illumina DNA Prep tagmentation kit and unique dual indexes. Sequencing was performed on the Illumina NextSeq2000 platform using a 300-cycle flow cell kit, producing 2x150bp paired reads. 1-2% PhiX control was spiked into the run to support optimal base calling. Read demultiplexing, read trimming, and run analytics were performed using DRAGEN v3.10.12.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20950249">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20950249</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40858150</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>LJ_1855</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>NextSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX24174297" alias="LG_1673">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX24174297</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14362661">LG_1673</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Lactobacillus gasseri UMB1673</TITLE>
    <STUDY_REF accession="SRP072679">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP072679</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA316969</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA was extracted from liquid culture using the Qiagen DNeasy Blood and Tissue Microbial Kit following the manufacturers protocol for Gram-positive bacteria. DNA was sent to SeqCoast Genomics LLC (Portsmouth, NH USA) for library preparation and sequencing. Samples were prepared for whole genome sequencing using an Illumina DNA Prep tagmentation kit and unique dual indexes. Sequencing was performed on the Illumina NextSeq2000 platform using a 300-cycle flow cell kit, producing 2x150bp paired reads. 1-2% PhiX control was spiked into the run to support optimal base calling. Read demultiplexing, read trimming, and run analytics were performed using DRAGEN v3.10.12.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20950250">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20950250</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN40858151</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>LG_1673</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>NextSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
