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      <PRIMARY_ID>SRX18251854</PRIMARY_ID>
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    </IDENTIFIERS>
    <TITLE>DNA-Seq of PAHs-contaminated soil bacteria, biological replicate 1</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP407804</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>Library construction was performed using the NEBNext Ultra IIDNA Library Prep Kit.Paired-end reads were merged using FLASH when at least some of the reads overlap with the reads generated from the opposite end of the same DNA fragment, and the splicing sequences were called Raw Tags. Quality filtering on the raw tags were performed using the fastp (Version 0.20.0) software to obtain high-quality Clean Tags.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS15746301</PRIMARY_ID>
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        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX18251855</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12261011">FKDO210422747-1A</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA-Seq of PAHs-contaminated soil bacteria, biological replicate 2</TITLE>
    <STUDY_REF accession="SRP407804">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407804</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12261011">bp0</SUBMITTER_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Library construction was performed using the NEBNext Ultra IIDNA Library Prep Kit.Paired-end reads were merged using FLASH when at least some of the reads overlap with the reads generated from the opposite end of the same DNA fragment, and the splicing sequences were called Raw Tags. Quality filtering on the raw tags were performed using the fastp (Version 0.20.1) software to obtain high-quality Clean Tags.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS15746302</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|liyuting0804@orcid">CK2</SUBMITTER_ID>
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        <LIBRARY_NAME>FKDO210422747-1A</LIBRARY_NAME>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX18251856</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12261011">FKDO210422759-1A</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA-Seq of PAHs and PBS-contaminated soil bacteria, biological replicate 2</TITLE>
    <STUDY_REF accession="SRP407804">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407804</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12261011">bp0</SUBMITTER_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Library construction was performed using the NEBNext Ultra IIDNA Library Prep Kit.Paired-end reads were merged using FLASH when at least some of the reads overlap with the reads generated from the opposite end of the same DNA fragment, and the splicing sequences were called Raw Tags. Quality filtering on the raw tags were performed using the fastp (Version 0.20.10) software to obtain high-quality Clean Tags.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS15746303</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|liyuting0804@orcid">PBS2</SUBMITTER_ID>
        </IDENTIFIERS>
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        <LIBRARY_NAME>FKDO210422759-1A</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX18251857</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12261011">FKDO210422760-1A</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA-Seq of PAHs and PBS-contaminated soil bacteria, biological replicate 3</TITLE>
    <STUDY_REF accession="SRP407804">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407804</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12261011">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library construction was performed using the NEBNext Ultra IIDNA Library Prep Kit.Paired-end reads were merged using FLASH when at least some of the reads overlap with the reads generated from the opposite end of the same DNA fragment, and the splicing sequences were called Raw Tags. Quality filtering on the raw tags were performed using the fastp (Version 0.20.11) software to obtain high-quality Clean Tags.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15746304">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15746304</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|liyuting0804@orcid">PBS3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FKDO210422760-1A</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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  <EXPERIMENT accession="SRX18251858" alias="FKDO210422755-1A">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18251858</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12261011">FKDO210422755-1A</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA-Seq of PAHs and PBAT-contaminated soil bacteria, biological replicate 1</TITLE>
    <STUDY_REF accession="SRP407804">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407804</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12261011">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library construction was performed using the NEBNext Ultra IIDNA Library Prep Kit.Paired-end reads were merged using FLASH when at least some of the reads overlap with the reads generated from the opposite end of the same DNA fragment, and the splicing sequences were called Raw Tags. Quality filtering on the raw tags were performed using the fastp (Version 0.20.12) software to obtain high-quality Clean Tags.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15746305">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15746305</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|liyuting0804@orcid">PBAT1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FKDO210422755-1A</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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  <EXPERIMENT accession="SRX18251859" alias="FKDO210422756-1A">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18251859</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12261011">FKDO210422756-1A</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA-Seq of PAHs and PBAT-contaminated soil bacteria, biological replicate 2</TITLE>
    <STUDY_REF accession="SRP407804">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407804</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12261011">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library construction was performed using the NEBNext Ultra IIDNA Library Prep Kit.Paired-end reads were merged using FLASH when at least some of the reads overlap with the reads generated from the opposite end of the same DNA fragment, and the splicing sequences were called Raw Tags. Quality filtering on the raw tags were performed using the fastp (Version 0.20.13) software to obtain high-quality Clean Tags.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS15746306</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|liyuting0804@orcid">PBAT2</SUBMITTER_ID>
        </IDENTIFIERS>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FKDO210422756-1A</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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  <EXPERIMENT accession="SRX18251860" alias="FKDO210422757-1A">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18251860</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12261011">FKDO210422757-1A</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA-Seq of PAHs and PBAT-contaminated soil bacteria, biological replicate 3</TITLE>
    <STUDY_REF accession="SRP407804">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407804</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12261011">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library construction was performed using the NEBNext Ultra IIDNA Library Prep Kit.Paired-end reads were merged using FLASH when at least some of the reads overlap with the reads generated from the opposite end of the same DNA fragment, and the splicing sequences were called Raw Tags. Quality filtering on the raw tags were performed using the fastp (Version 0.20.14) software to obtain high-quality Clean Tags.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS15746307</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|liyuting0804@orcid">PBAT3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FKDO210422757-1A</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX18251861</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12261011">FKDO210422752-1A</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA-Seq of PAHs and LDPE-contaminated soil bacteria, biological replicate 1</TITLE>
    <STUDY_REF accession="SRP407804">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407804</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12261011">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library construction was performed using the NEBNext Ultra IIDNA Library Prep Kit.Paired-end reads were merged using FLASH when at least some of the reads overlap with the reads generated from the opposite end of the same DNA fragment, and the splicing sequences were called Raw Tags. Quality filtering on the raw tags were performed using the fastp (Version 0.20.15) software to obtain high-quality Clean Tags.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS15746308</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|liyuting0804@orcid">LDPE1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FKDO210422752-1A</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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      <PRIMARY_ID>SRX18251862</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12261011">FKDO210422753-1A</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA-Seq of PAHs and LDPE-contaminated soil bacteria, biological replicate 2</TITLE>
    <STUDY_REF accession="SRP407804">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407804</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12261011">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library construction was performed using the NEBNext Ultra IIDNA Library Prep Kit.Paired-end reads were merged using FLASH when at least some of the reads overlap with the reads generated from the opposite end of the same DNA fragment, and the splicing sequences were called Raw Tags. Quality filtering on the raw tags were performed using the fastp (Version 0.20.16) software to obtain high-quality Clean Tags.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS15746309</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|liyuting0804@orcid">LDPE2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
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        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <PRIMARY_ID>SRX18251863</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12261011">FKDO210422754-1A</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA-Seq of PAHs and LDPE-contaminated soil bacteria, biological replicate 3</TITLE>
    <STUDY_REF accession="SRP407804">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407804</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12261011">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library construction was performed using the NEBNext Ultra IIDNA Library Prep Kit.Paired-end reads were merged using FLASH when at least some of the reads overlap with the reads generated from the opposite end of the same DNA fragment, and the splicing sequences were called Raw Tags. Quality filtering on the raw tags were performed using the fastp (Version 0.20.17) software to obtain high-quality Clean Tags.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS15746310</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|liyuting0804@orcid">LDPE3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FKDO210422754-1A</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX18251864</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12261011">FKDO210422748-1A</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA-Seq of PAHs-contaminated soil bacteria, biological replicate 3</TITLE>
    <STUDY_REF accession="SRP407804">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407804</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12261011">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library construction was performed using the NEBNext Ultra IIDNA Library Prep Kit.Paired-end reads were merged using FLASH when at least some of the reads overlap with the reads generated from the opposite end of the same DNA fragment, and the splicing sequences were called Raw Tags. Quality filtering on the raw tags were performed using the fastp (Version 0.20.2) software to obtain high-quality Clean Tags.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15746311">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15746311</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|liyuting0804@orcid">CK3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FKDO210422748-1A</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18251865" alias="FKDO210422749-1A">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18251865</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12261011">FKDO210422749-1A</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA-Seq of PAHs and PLA-contaminated soil bacteria, biological replicate 1</TITLE>
    <STUDY_REF accession="SRP407804">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407804</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12261011">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library construction was performed using the NEBNext Ultra IIDNA Library Prep Kit.Paired-end reads were merged using FLASH when at least some of the reads overlap with the reads generated from the opposite end of the same DNA fragment, and the splicing sequences were called Raw Tags. Quality filtering on the raw tags were performed using the fastp (Version 0.20.3) software to obtain high-quality Clean Tags.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15746312">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15746312</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|liyuting0804@orcid">PLA1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FKDO210422749-1A</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18251866" alias="FKDO210422750-1A">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18251866</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12261011">FKDO210422750-1A</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA-Seq of PAHs and PLA-contaminated soil bacteria, biological replicate 2</TITLE>
    <STUDY_REF accession="SRP407804">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407804</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12261011">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library construction was performed using the NEBNext Ultra IIDNA Library Prep Kit.Paired-end reads were merged using FLASH when at least some of the reads overlap with the reads generated from the opposite end of the same DNA fragment, and the splicing sequences were called Raw Tags. Quality filtering on the raw tags were performed using the fastp (Version 0.20.4) software to obtain high-quality Clean Tags.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15746313">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15746313</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|liyuting0804@orcid">PLA2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FKDO210422750-1A</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18251867" alias="FKDO210422751-1A">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18251867</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12261011">FKDO210422751-1A</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA-Seq of PAHs and PLA-contaminated soil bacteria, biological replicate 3</TITLE>
    <STUDY_REF accession="SRP407804">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407804</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12261011">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library construction was performed using the NEBNext Ultra IIDNA Library Prep Kit.Paired-end reads were merged using FLASH when at least some of the reads overlap with the reads generated from the opposite end of the same DNA fragment, and the splicing sequences were called Raw Tags. Quality filtering on the raw tags were performed using the fastp (Version 0.20.5) software to obtain high-quality Clean Tags.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15746314">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15746314</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|liyuting0804@orcid">PLA3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FKDO210422751-1A</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18251868" alias="FKDO210422761-1A">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18251868</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12261011">FKDO210422761-1A</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA-Seq of PAHs and PHB-contaminated soil bacteria, biological replicate 1</TITLE>
    <STUDY_REF accession="SRP407804">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407804</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12261011">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library construction was performed using the NEBNext Ultra IIDNA Library Prep Kit.Paired-end reads were merged using FLASH when at least some of the reads overlap with the reads generated from the opposite end of the same DNA fragment, and the splicing sequences were called Raw Tags. Quality filtering on the raw tags were performed using the fastp (Version 0.20.6) software to obtain high-quality Clean Tags.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15746315">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15746315</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|liyuting0804@orcid">PHB1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FKDO210422761-1A</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18251869" alias="FKDO210422762-1A">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18251869</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12261011">FKDO210422762-1A</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA-Seq of PAHs and PHB-contaminated soil bacteria, biological replicate 2</TITLE>
    <STUDY_REF accession="SRP407804">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407804</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12261011">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library construction was performed using the NEBNext Ultra IIDNA Library Prep Kit.Paired-end reads were merged using FLASH when at least some of the reads overlap with the reads generated from the opposite end of the same DNA fragment, and the splicing sequences were called Raw Tags. Quality filtering on the raw tags were performed using the fastp (Version 0.20.7) software to obtain high-quality Clean Tags.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15746316">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15746316</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|liyuting0804@orcid">PHB2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FKDO210422762-1A</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18251870" alias="FKDO210422763-1A">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18251870</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12261011">FKDO210422763-1A</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA-Seq of PAHs and PHB-contaminated soil bacteria, biological replicate 3</TITLE>
    <STUDY_REF accession="SRP407804">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407804</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12261011">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library construction was performed using the NEBNext Ultra IIDNA Library Prep Kit.Paired-end reads were merged using FLASH when at least some of the reads overlap with the reads generated from the opposite end of the same DNA fragment, and the splicing sequences were called Raw Tags. Quality filtering on the raw tags were performed using the fastp (Version 0.20.8) software to obtain high-quality Clean Tags.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15746317">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15746317</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|liyuting0804@orcid">PHB3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FKDO210422763-1A</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18251871" alias="FKDO210422758-1A">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18251871</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12261011">FKDO210422758-1A</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA-Seq of PAHs and PBS-contaminated soil bacteria, biological replicate 1</TITLE>
    <STUDY_REF accession="SRP407804">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407804</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12261011">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library construction was performed using the NEBNext Ultra IIDNA Library Prep Kit.Paired-end reads were merged using FLASH when at least some of the reads overlap with the reads generated from the opposite end of the same DNA fragment, and the splicing sequences were called Raw Tags. Quality filtering on the raw tags were performed using the fastp (Version 0.20.9) software to obtain high-quality Clean Tags.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15746318">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15746318</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|liyuting0804@orcid">PBS1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FKDO210422758-1A</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
