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    <TITLE>16srDNA of rumen fluid:Chinese Luxi Yellow beef cattle</TITLE>
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  <EXPERIMENT accession="SRX4638203" alias="DH5">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4638203</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4479430">DH5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16srDNA of rumen fluid:high yield Holstein dairy cow</TITLE>
    <STUDY_REF accession="SRP159535">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP159535</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4479430">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The samples were slowly thawed at 4C. Total DNA was extracted from the rumen fluid samples using the Stool DNA Isolation Kit (Tiangen, Beijing, China). DNA samples were quantified using a Nanodrop spectrophotometer (Nyxor Biotech, Paris, France), and then transferred to BGI Genomics for V4 region of the 16S rDNA gene sequencing with PE250 Miseq. The PCR primer used for 16S rDNA amplicon libraries was 515F-810R.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3736869">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3736869</PRIMARY_ID>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4638204" alias="DH6">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4638204</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4479430">DH6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16srDNA of rumen fluid:high yield Holstein dairy cow</TITLE>
    <STUDY_REF accession="SRP159535">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP159535</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4479430">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The samples were slowly thawed at 4C. Total DNA was extracted from the rumen fluid samples using the Stool DNA Isolation Kit (Tiangen, Beijing, China). DNA samples were quantified using a Nanodrop spectrophotometer (Nyxor Biotech, Paris, France), and then transferred to BGI Genomics for V4 region of the 16S rDNA gene sequencing with PE250 Miseq. The PCR primer used for 16S rDNA amplicon libraries was 515F-811R.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3736870">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3736870</PRIMARY_ID>
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      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DH6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4638205" alias="DL1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4638205</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4479430">DL1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16srDNA of rumen fluid:low yield Holstein dairy cow</TITLE>
    <STUDY_REF accession="SRP159535">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP159535</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4479430">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The samples were slowly thawed at 4C. Total DNA was extracted from the rumen fluid samples using the Stool DNA Isolation Kit (Tiangen, Beijing, China). DNA samples were quantified using a Nanodrop spectrophotometer (Nyxor Biotech, Paris, France), and then transferred to BGI Genomics for V4 region of the 16S rDNA gene sequencing with PE250 Miseq. The PCR primer used for 16S rDNA amplicon libraries was 515F-812R.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3736871">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3736871</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|1zt1">DL1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DL1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4638206" alias="DL2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4638206</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4479430">DL2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16srDNA of rumen fluid:low yield Holstein dairy cow</TITLE>
    <STUDY_REF accession="SRP159535">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP159535</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4479430">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The samples were slowly thawed at 4C. Total DNA was extracted from the rumen fluid samples using the Stool DNA Isolation Kit (Tiangen, Beijing, China). DNA samples were quantified using a Nanodrop spectrophotometer (Nyxor Biotech, Paris, France), and then transferred to BGI Genomics for V4 region of the 16S rDNA gene sequencing with PE250 Miseq. The PCR primer used for 16S rDNA amplicon libraries was 515F-813R.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3736872">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3736872</PRIMARY_ID>
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        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DL2</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 MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4638207" alias="DL3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4638207</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4479430">DL3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16srDNA of rumen fluid:low yield Holstein dairy cow</TITLE>
    <STUDY_REF accession="SRP159535">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP159535</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4479430">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The samples were slowly thawed at 4C. Total DNA was extracted from the rumen fluid samples using the Stool DNA Isolation Kit (Tiangen, Beijing, China). DNA samples were quantified using a Nanodrop spectrophotometer (Nyxor Biotech, Paris, France), and then transferred to BGI Genomics for V4 region of the 16S rDNA gene sequencing with PE250 Miseq. The PCR primer used for 16S rDNA amplicon libraries was 515F-814R.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3736873">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3736873</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|1zt1">DL3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DL3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4638208" alias="DL4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4638208</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4479430">DL4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16srDNA of rumen fluid:low yield Holstein dairy cow</TITLE>
    <STUDY_REF accession="SRP159535">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP159535</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4479430">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The samples were slowly thawed at 4C. Total DNA was extracted from the rumen fluid samples using the Stool DNA Isolation Kit (Tiangen, Beijing, China). DNA samples were quantified using a Nanodrop spectrophotometer (Nyxor Biotech, Paris, France), and then transferred to BGI Genomics for V4 region of the 16S rDNA gene sequencing with PE250 Miseq. The PCR primer used for 16S rDNA amplicon libraries was 515F-815R.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3736874">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3736874</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|1zt1">DL4</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DL4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4638209" alias="H2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4638209</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4479430">H2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16srDNA of rumen fluid:Chinese Bohai Black beef cattle</TITLE>
    <STUDY_REF accession="SRP159535">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP159535</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4479430">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The samples were slowly thawed at 4C. Total DNA was extracted from the rumen fluid samples using the Stool DNA Isolation Kit (Tiangen, Beijing, China). DNA samples were quantified using a Nanodrop spectrophotometer (Nyxor Biotech, Paris, France), and then transferred to BGI Genomics for V4 region of the 16S rDNA gene sequencing with PE250 Miseq. The PCR primer used for 16S rDNA amplicon libraries was 515F-824R.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3736885">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3736885</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|1zt1">H2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>H2</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 MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4638210" alias="H3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4638210</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4479430">H3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16srDNA of rumen fluid:Chinese Bohai Black beef cattle</TITLE>
    <STUDY_REF accession="SRP159535">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP159535</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4479430">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The samples were slowly thawed at 4C. Total DNA was extracted from the rumen fluid samples using the Stool DNA Isolation Kit (Tiangen, Beijing, China). DNA samples were quantified using a Nanodrop spectrophotometer (Nyxor Biotech, Paris, France), and then transferred to BGI Genomics for V4 region of the 16S rDNA gene sequencing with PE250 Miseq. The PCR primer used for 16S rDNA amplicon libraries was 515F-825R.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3736876">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3736876</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|1zt1">H3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>H3</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 MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4638211" alias="G1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4638211</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4479430">G1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16srDNA of rumen fluid:Chinese Laoshan milk goat</TITLE>
    <STUDY_REF accession="SRP159535">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP159535</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4479430">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The samples were slowly thawed at 4C. Total DNA was extracted from the rumen fluid samples using the Stool DNA Isolation Kit (Tiangen, Beijing, China). DNA samples were quantified using a Nanodrop spectrophotometer (Nyxor Biotech, Paris, France), and then transferred to BGI Genomics for V4 region of the 16S rDNA gene sequencing with PE250 Miseq. The PCR primer used for 16S rDNA amplicon libraries was 515F-818R.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3736877">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3736877</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|1zt1">G1</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>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX4638212</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4479430">G3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16srDNA of rumen fluid:Chinese Laoshan milk goat</TITLE>
    <STUDY_REF accession="SRP159535">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP159535</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4479430">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The samples were slowly thawed at 4C. Total DNA was extracted from the rumen fluid samples using the Stool DNA Isolation Kit (Tiangen, Beijing, China). DNA samples were quantified using a Nanodrop spectrophotometer (Nyxor Biotech, Paris, France), and then transferred to BGI Genomics for V4 region of the 16S rDNA gene sequencing with PE250 Miseq. The PCR primer used for 16S rDNA amplicon libraries was 515F-819R.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3736878">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3736878</PRIMARY_ID>
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        </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>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX4638213</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4479430">DL5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16srDNA of rumen fluid:low yield Holstein dairy cow</TITLE>
    <STUDY_REF accession="SRP159535">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP159535</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4479430">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The samples were slowly thawed at 4C. Total DNA was extracted from the rumen fluid samples using the Stool DNA Isolation Kit (Tiangen, Beijing, China). DNA samples were quantified using a Nanodrop spectrophotometer (Nyxor Biotech, Paris, France), and then transferred to BGI Genomics for V4 region of the 16S rDNA gene sequencing with PE250 Miseq. The PCR primer used for 16S rDNA amplicon libraries was 515F-816R.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS3736879</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|1zt1">DL5</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>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX4638214</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4479430">DL6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16srDNA of rumen fluid:low yield Holstein dairy cow</TITLE>
    <STUDY_REF accession="SRP159535">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP159535</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4479430">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The samples were slowly thawed at 4C. Total DNA was extracted from the rumen fluid samples using the Stool DNA Isolation Kit (Tiangen, Beijing, China). DNA samples were quantified using a Nanodrop spectrophotometer (Nyxor Biotech, Paris, France), and then transferred to BGI Genomics for V4 region of the 16S rDNA gene sequencing with PE250 Miseq. The PCR primer used for 16S rDNA amplicon libraries was 515F-817R.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS3736880</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|1zt1">DL6</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>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4638215" alias="G6">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4638215</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4479430">G6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16srDNA of rumen fluid:Chinese Laoshan milk goat</TITLE>
    <STUDY_REF accession="SRP159535">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP159535</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4479430">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The samples were slowly thawed at 4C. Total DNA was extracted from the rumen fluid samples using the Stool DNA Isolation Kit (Tiangen, Beijing, China). DNA samples were quantified using a Nanodrop spectrophotometer (Nyxor Biotech, Paris, France), and then transferred to BGI Genomics for V4 region of the 16S rDNA gene sequencing with PE250 Miseq. The PCR primer used for 16S rDNA amplicon libraries was 515F-822R.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3736881">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3736881</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|1zt1">G6</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>G6</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 MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4638216" alias="H1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4638216</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4479430">H1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16srDNA of rumen fluid:Chinese Bohai Black beef cattle</TITLE>
    <STUDY_REF accession="SRP159535">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP159535</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4479430">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The samples were slowly thawed at 4C. Total DNA was extracted from the rumen fluid samples using the Stool DNA Isolation Kit (Tiangen, Beijing, China). DNA samples were quantified using a Nanodrop spectrophotometer (Nyxor Biotech, Paris, France), and then transferred to BGI Genomics for V4 region of the 16S rDNA gene sequencing with PE250 Miseq. The PCR primer used for 16S rDNA amplicon libraries was 515F-823R.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3736882">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3736882</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|1zt1">H1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>H1</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 MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4638217" alias="G4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4638217</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4479430">G4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16srDNA of rumen fluid:Chinese Laoshan milk goat</TITLE>
    <STUDY_REF accession="SRP159535">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP159535</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4479430">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The samples were slowly thawed at 4C. Total DNA was extracted from the rumen fluid samples using the Stool DNA Isolation Kit (Tiangen, Beijing, China). DNA samples were quantified using a Nanodrop spectrophotometer (Nyxor Biotech, Paris, France), and then transferred to BGI Genomics for V4 region of the 16S rDNA gene sequencing with PE250 Miseq. The PCR primer used for 16S rDNA amplicon libraries was 515F-820R.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3736883">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3736883</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|1zt1">G4</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>G4</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 MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4638218" alias="G5">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4638218</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4479430">G5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16srDNA of rumen fluid:Chinese Laoshan milk goat</TITLE>
    <STUDY_REF accession="SRP159535">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP159535</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4479430">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The samples were slowly thawed at 4C. Total DNA was extracted from the rumen fluid samples using the Stool DNA Isolation Kit (Tiangen, Beijing, China). DNA samples were quantified using a Nanodrop spectrophotometer (Nyxor Biotech, Paris, France), and then transferred to BGI Genomics for V4 region of the 16S rDNA gene sequencing with PE250 Miseq. The PCR primer used for 16S rDNA amplicon libraries was 515F-821R.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3736884">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3736884</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|1zt1">G5</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>G5</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 MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
