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      </ILLUMINA>
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    <TITLE>16S rRNA seqences from black pepper (Piper nigrum L.) rhizosphere in Vietnam</TITLE>
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      <DESIGN_DESCRIPTION>Total genomic DNA was extracted from the rhizospher of black pepper plants. Amplification of the 16S region was performed using a PCR approach specifically designed for Illumina instruments. The PCR reaction was purified and barcoded amplicons were pooled in equimolar concentration prior to sequencing on the illumina Miseq platform.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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      <DESIGN_DESCRIPTION>Total genomic DNA was extracted from the rhizospher of black pepper plants. Amplification of the 16S region was performed using a PCR approach specifically designed for Illumina instruments. The PCR reaction was purified and barcoded amplicons were pooled in equimolar concentration prior to sequencing on the illumina Miseq platform.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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    <TITLE>16S rRNA seqences from black pepper (Piper nigrum L.) rhizosphere in Vietnam</TITLE>
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      <DESIGN_DESCRIPTION>Total genomic DNA was extracted from the rhizospher of black pepper plants. Amplification of the 16S region was performed using a PCR approach specifically designed for Illumina instruments. The PCR reaction was purified and barcoded amplicons were pooled in equimolar concentration prior to sequencing on the illumina Miseq platform.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS15857002</PRIMARY_ID>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX18370618</PRIMARY_ID>
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    <TITLE>16S rRNA seqences from black pepper (Piper nigrum L.) rhizosphere in Vietnam</TITLE>
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        <PRIMARY_ID>SRP409557</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Total genomic DNA was extracted from the rhizospher of black pepper plants. Amplification of the 16S region was performed using a PCR approach specifically designed for Illumina instruments. The PCR reaction was purified and barcoded amplicons were pooled in equimolar concentration prior to sequencing on the illumina Miseq platform.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS15857003</PRIMARY_ID>
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        </LIBRARY_LAYOUT>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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      <PRIMARY_ID>SRX18370619</PRIMARY_ID>
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    <TITLE>16S rRNA seqences from black pepper (Piper nigrum L.) rhizosphere in Vietnam</TITLE>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Total genomic DNA was extracted from the rhizospher of black pepper plants. Amplification of the 16S region was performed using a PCR approach specifically designed for Illumina instruments. The PCR reaction was purified and barcoded amplicons were pooled in equimolar concentration prior to sequencing on the illumina Miseq platform.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS15857004</PRIMARY_ID>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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        </LIBRARY_LAYOUT>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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    </PLATFORM>
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      <PRIMARY_ID>SRX18370620</PRIMARY_ID>
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    <TITLE>16S rRNA seqences from black pepper (Piper nigrum L.) rhizosphere in Vietnam</TITLE>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Total genomic DNA was extracted from the rhizospher of black pepper plants. Amplification of the 16S region was performed using a PCR approach specifically designed for Illumina instruments. The PCR reaction was purified and barcoded amplicons were pooled in equimolar concentration prior to sequencing on the illumina Miseq platform.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX18370621</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Total genomic DNA was extracted from the rhizospher of black pepper plants. Amplification of the 16S region was performed using a PCR approach specifically designed for Illumina instruments. The PCR reaction was purified and barcoded amplicons were pooled in equimolar concentration prior to sequencing on the illumina Miseq platform.</DESIGN_DESCRIPTION>
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      <PRIMARY_ID>SRX18370622</PRIMARY_ID>
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    <TITLE>16S rRNA seqences from black pepper (Piper nigrum L.) rhizosphere in Vietnam</TITLE>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Total genomic DNA was extracted from the rhizospher of black pepper plants. Amplification of the 16S region was performed using a PCR approach specifically designed for Illumina instruments. The PCR reaction was purified and barcoded amplicons were pooled in equimolar concentration prior to sequencing on the illumina Miseq platform.</DESIGN_DESCRIPTION>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Total genomic DNA was extracted from the rhizospher of black pepper plants. Amplification of the 16S region was performed using a PCR approach specifically designed for Illumina instruments. The PCR reaction was purified and barcoded amplicons were pooled in equimolar concentration prior to sequencing on the illumina Miseq platform.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Total genomic DNA was extracted from the rhizospher of black pepper plants. Amplification of the 16S region was performed using a PCR approach specifically designed for Illumina instruments. The PCR reaction was purified and barcoded amplicons were pooled in equimolar concentration prior to sequencing on the illumina Miseq platform.</DESIGN_DESCRIPTION>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Total genomic DNA was extracted from the rhizospher of black pepper plants. Amplification of the 16S region was performed using a PCR approach specifically designed for Illumina instruments. The PCR reaction was purified and barcoded amplicons were pooled in equimolar concentration prior to sequencing on the illumina Miseq platform.</DESIGN_DESCRIPTION>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Total genomic DNA was extracted from the rhizospher of black pepper plants. Amplification of the 16S region was performed using a PCR approach specifically designed for Illumina instruments. The PCR reaction was purified and barcoded amplicons were pooled in equimolar concentration prior to sequencing on the illumina Miseq platform.</DESIGN_DESCRIPTION>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Total genomic DNA was extracted from the rhizospher of black pepper plants. Amplification of the 16S region was performed using a PCR approach specifically designed for Illumina instruments. The PCR reaction was purified and barcoded amplicons were pooled in equimolar concentration prior to sequencing on the illumina Miseq platform.</DESIGN_DESCRIPTION>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX18370628</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12324163">PG-16s-p1-H2</SUBMITTER_ID>
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    <TITLE>16S rRNA seqences from black pepper (Piper nigrum L.) rhizosphere in Vietnam</TITLE>
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        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PG-16s-p2-B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</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>
