<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX22250948" alias="D2-1-NA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250948</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-1-NA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304636">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304636</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-1-NA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-1-NA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250949" alias="D2-2-NA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250949</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-2-NA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304637">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304637</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-2-NA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-2-NA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250950" alias="D2-14-NA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250950</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-14-NA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304638">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304638</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-14-NA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-14-NA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250951" alias="D2-16-NA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250951</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-16-NA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304639">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304639</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-16-NA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-16-NA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250952" alias="D2-17-NA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250952</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-17-NA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304640">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304640</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-17-NA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-17-NA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250953" alias="D2-19-NA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250953</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-19-NA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304641">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304641</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-19-NA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-19-NA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250954" alias="D2-20-NA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250954</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-20-NA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304642">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304642</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-20-NA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-20-NA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250955" alias="D2-1-Sn">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250955</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-1-Sn</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304643">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304643</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-1-Sn</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-1-Sn</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250956" alias="D2-2-Sn">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250956</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-2-Sn</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304644">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304644</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-2-Sn</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-2-Sn</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250957" alias="D2-4-Sn">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250957</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-4-Sn</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304645">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304645</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-4-Sn</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-4-Sn</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250958" alias="D2-5-Sn">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250958</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-5-Sn</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304646">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304646</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-5-Sn</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-5-Sn</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250959" alias="D2-6-Sn">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250959</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-6-Sn</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304647">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304647</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-6-Sn</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-6-Sn</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250960" alias="D2-4-NA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250960</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-4-NA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304648">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304648</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-4-NA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-4-NA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250961" alias="D2-8-Sn">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250961</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-8-Sn</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304649">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304649</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-8-Sn</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-8-Sn</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250962" alias="D2-9-Sn">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250962</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-9-Sn</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304650">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304650</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-9-Sn</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-9-Sn</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250963" alias="D2-11-Sn">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250963</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-11-Sn</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304651">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304651</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-11-Sn</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-11-Sn</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250964" alias="D2-12-Sn">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250964</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-12-Sn</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304652">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304652</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-12-Sn</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-12-Sn</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250965" alias="D2-13-Sn">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250965</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-13-Sn</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304653">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304653</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-13-Sn</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-13-Sn</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250966" alias="D2-14-Sn">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250966</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-14-Sn</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304655">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304655</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-14-Sn</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-14-Sn</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250967" alias="D2-16-Sn">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250967</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-16-Sn</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304654">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304654</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-16-Sn</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-16-Sn</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250968" alias="D2-17-Sn">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250968</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-17-Sn</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304656">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304656</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-17-Sn</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-17-Sn</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250969" alias="D2-19-Sn">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250969</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-19-Sn</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304657">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304657</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-19-Sn</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-19-Sn</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250970" alias="D2-20-Sn">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250970</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-20-Sn</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304658">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304658</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-20-Sn</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-20-Sn</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250971" alias="D2-5-NA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250971</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-5-NA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304659">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304659</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-5-NA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-5-NA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250972" alias="D2-1-Zn">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250972</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-1-Zn</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304660">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304660</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-1-Zn</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-1-Zn</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250973" alias="D2-2-Zn">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250973</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-2-Zn</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304661">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304661</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-2-Zn</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-2-Zn</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250974" alias="D2-4-Zn">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250974</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-4-Zn</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304662">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304662</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-4-Zn</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-4-Zn</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250975" alias="D2-5-Zn">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250975</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-5-Zn</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304663">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304663</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-5-Zn</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-5-Zn</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250976" alias="D2-6-Zn">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250976</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-6-Zn</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304665">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304665</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-6-Zn</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-6-Zn</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250977" alias="D2-8-Zn">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250977</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-8-Zn</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304664">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304664</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-8-Zn</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-8-Zn</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250978" alias="D2-9-Zn">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250978</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-9-Zn</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304667">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304667</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-9-Zn</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-9-Zn</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250979" alias="D2-11-Zn">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250979</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-11-Zn</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304666">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304666</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-11-Zn</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-11-Zn</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250980" alias="D2-12-Zn">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250980</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-12-Zn</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304668">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304668</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-12-Zn</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-12-Zn</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250981" alias="D2-13-Zn">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250981</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-13-Zn</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304669">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304669</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-13-Zn</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-13-Zn</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250982" alias="D2-6-NA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250982</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-6-NA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304671">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304671</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-6-NA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-6-NA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250983" alias="D2-14-Zn">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250983</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-14-Zn</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304670">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304670</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-14-Zn</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-14-Zn</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250984" alias="D2-16-Zn">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250984</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-16-Zn</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304672">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304672</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-16-Zn</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-16-Zn</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250985" alias="D2-17-Zn">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250985</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-17-Zn</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304673">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304673</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-17-Zn</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-17-Zn</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250986" alias="D2-19-Zn">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250986</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-19-Zn</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304674">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304674</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-19-Zn</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-19-Zn</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250987" alias="D2-20-Zn">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250987</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-20-Zn</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304675">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304675</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-20-Zn</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-20-Zn</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250988" alias="PC">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250988</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">PC</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304676">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304676</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">PC</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PC</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250989" alias="NC_1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250989</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">NC_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304677">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304677</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">NC_1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NC_1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250990" alias="NC_2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250990</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">NC_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304678">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304678</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">NC_2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NC_2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250991" alias="D2-8-NA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250991</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-8-NA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304679">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304679</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-8-NA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-8-NA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250992" alias="D2-9-NA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250992</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-9-NA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304680">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304680</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-9-NA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-9-NA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250993" alias="D2-11-NA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250993</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-11-NA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304681">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304681</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-11-NA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-11-NA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250994" alias="D2-12-NA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250994</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-12-NA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304682">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304682</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-12-NA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-12-NA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22250995" alias="D2-13-NA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22250995</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13920835">D2-13-NA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2bRAD-M of oral microbiome</TITLE>
    <STUDY_REF accession="SRP468851">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468851</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13920835">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA was extracted from treated biofilms using the TIANamp Micro DNA Kit, and carrier RNA was added to enhance the yield. The extracted DNA was then subjected to 2bRAD library preparation, including digestion with BcgI restriction enzyme, ligation with library-specific adaptors, PCR amplification, purification, and sequencing on the Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19304683">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19304683</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dillonchewwx@gmail.com">D2-13-NA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2-13-NA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RAD-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
