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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX4286739" alias="14">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4286739</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4196370">14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>14 fastq</TITLE>
    <STUDY_REF accession="SRP151178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP151178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA477609</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA extraction is the first step and the next step is 16S rRNA gene amplification by PCR and then 29S gene library construction,quantification,and sequencing, finally do the Sequence processing</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3450774">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3450774</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN09475414</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4286740" alias="13">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4286740</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4196370">13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>13 fastq</TITLE>
    <STUDY_REF accession="SRP151178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP151178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA477609</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA extraction is the first step and the next step is 16S rRNA gene amplification by PCR and then 28S gene library construction,quantification,and sequencing, finally do the Sequence processing</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3450777">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3450777</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN09475413</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4286741" alias="12">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4286741</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4196370">12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>12 fastq</TITLE>
    <STUDY_REF accession="SRP151178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP151178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA477609</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA extraction is the first step and the next step is 16S rRNA gene amplification by PCR and then 27S gene library construction,quantification,and sequencing, finally do the Sequence processing</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3450775">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3450775</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN09475412</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4286742" alias="11">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4286742</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4196370">11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>11 fastq</TITLE>
    <STUDY_REF accession="SRP151178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP151178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA477609</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA extraction is the first step and the next step is 16S rRNA gene amplification by PCR and then 26S gene library construction,quantification,and sequencing, finally do the Sequence processing</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3450776">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3450776</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN09475411</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4286743" alias="4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4286743</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4196370">4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>4 fastq</TITLE>
    <STUDY_REF accession="SRP151178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP151178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA477609</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA extraction is the first step and the next step is 16S rRNA gene amplification by PCR and then 19S gene library construction,quantification,and sequencing, finally do the Sequence processing</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3450783">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3450783</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN09475404</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4286744" alias="3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4286744</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4196370">3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>3 fastq</TITLE>
    <STUDY_REF accession="SRP151178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP151178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA477609</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA extraction is the first step and the next step is 16S rRNA gene amplification by PCR and then 18S gene library construction,quantification,and sequencing, finally do the Sequence processing</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3450778">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3450778</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN09475403</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4286745" alias="2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4286745</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4196370">2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>2 fastq</TITLE>
    <STUDY_REF accession="SRP151178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP151178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA477609</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA extraction is the first step and the next step is 16S rRNA gene amplification by PCR and then 17S gene library construction,quantification,and sequencing, finally do the Sequence processing</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3450779">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3450779</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN09475402</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4286746" alias="1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4286746</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4196370">1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>1 fastq</TITLE>
    <STUDY_REF accession="SRP151178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP151178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA477609</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA extraction is the first step and the next step is 16S rRNA gene amplification by PCR and then 16S gene library construction,quantification,and sequencing, finally do the Sequence processing</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3450781">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3450781</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN09475401</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4286747" alias="15">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4286747</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4196370">15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>15 fastq</TITLE>
    <STUDY_REF accession="SRP151178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP151178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA477609</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA extraction is the first step and the next step is 16S rRNA gene amplification by PCR and then 30S gene library construction,quantification,and sequencing, finally do the Sequence processing</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3450782">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3450782</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN09475415</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4286748" alias="6">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4286748</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4196370">6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>6 fastq</TITLE>
    <STUDY_REF accession="SRP151178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP151178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA477609</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA extraction is the first step and the next step is 16S rRNA gene amplification by PCR and then 21S gene library construction,quantification,and sequencing, finally do the Sequence processing</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3450784">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3450784</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN09475406</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4286749" alias="10">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4286749</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4196370">10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>10 fastq</TITLE>
    <STUDY_REF accession="SRP151178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP151178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA477609</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA extraction is the first step and the next step is 16S rRNA gene amplification by PCR and then 25S gene library construction,quantification,and sequencing, finally do the Sequence processing</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3450785">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3450785</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN09475410</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4286750" alias="9">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4286750</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4196370">9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>9 fastq</TITLE>
    <STUDY_REF accession="SRP151178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP151178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA477609</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA extraction is the first step and the next step is 16S rRNA gene amplification by PCR and then 24S gene library construction,quantification,and sequencing, finally do the Sequence processing</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3450786">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3450786</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN09475409</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4286751" alias="5">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4286751</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4196370">5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>5 fastq</TITLE>
    <STUDY_REF accession="SRP151178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP151178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA477609</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA extraction is the first step and the next step is 16S rRNA gene amplification by PCR and then 20S gene library construction,quantification,and sequencing, finally do the Sequence processing</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3450787">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3450787</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN09475405</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4286752" alias="7">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4286752</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4196370">7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>7 fastq</TITLE>
    <STUDY_REF accession="SRP151178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP151178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA477609</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA extraction is the first step and the next step is 16S rRNA gene amplification by PCR and then 22S gene library construction,quantification,and sequencing, finally do the Sequence processing</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3450788">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3450788</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN09475407</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4286753" alias="8">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4286753</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4196370">8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>8 fastq</TITLE>
    <STUDY_REF accession="SRP151178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP151178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA477609</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA extraction is the first step and the next step is 16S rRNA gene amplification by PCR and then 23S gene library construction,quantification,and sequencing, finally do the Sequence processing</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3450789">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3450789</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN09475408</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
