<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX3908239" alias="GD-C1-B">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3908239</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3878188">GD-C1-B</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Rhizospheric bacterica of cultivatedrice in Guangdong</TITLE>
    <STUDY_REF accession="SRP139050">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP139050</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA449026</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The primer pair used to amplify the V3-V4 hypervariable regions of the bacterial 16SrRNA genes was 341F (5 -CCTACGGGNGGCWGCAG-3 ) and 785R (5 -GACTACHVGGGTATCTAATCC-3 ) . The PCR program was as follows: 2 min at 95 C; 25 cycles of 30 s at 95 C, 30 s at 55 C, and 45 s at 72 C; and a final extension step at 72 C for 10 min.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3144108">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3144108</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08875358</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GD-C1-B</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3908240" alias="HN-W1-B">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3908240</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3878188">HN-W1-B</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Rhizospheric bacterica of wild rice in Hainan</TITLE>
    <STUDY_REF accession="SRP139050">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP139050</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA449026</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The primer pair used to amplify the V3-V4 hypervariable regions of the bacterial 16SrRNA genes was 341F (5 -CCTACGGGNGGCWGCAG-3 ) and 785R (5 -GACTACHVGGGTATCTAATCC-3 ) . The PCR program was as follows: 2 min at 95 C; 25 cycles of 30 s at 95 C, 30 s at 55 C, and 45 s at 72 C; and a final extension step at 72 C for 10 min.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3144109">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3144109</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08875356</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>HN-W1-B</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3908241" alias="HN-C1-B">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3908241</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3878188">HN-C1-B</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Rhizospheric bacterica of cultivated rice in Hainan</TITLE>
    <STUDY_REF accession="SRP139050">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP139050</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA449026</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The primer pair used to amplify the V3-V4 hypervariable regions of the bacterial 16SrRNA genes was 341F (5 -CCTACGGGNGGCWGCAG-3 ) and 785R (5 -GACTACHVGGGTATCTAATCC-3 ) . The PCR program was as follows: 2 min at 95 C; 25 cycles of 30 s at 95 C, 30 s at 55 C, and 45 s at 72 C; and a final extension step at 72 C for 10 min.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3144107">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3144107</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08875359</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>HN-C1-B</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3908242" alias="JX-C1-B">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3908242</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3878188">JX-C1-B</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Rhizospheric bacterica of cultivated rice in Jiangxi</TITLE>
    <STUDY_REF accession="SRP139050">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP139050</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA449026</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The primer pair used to amplify the V3-V4 hypervariable regions of the bacterial 16SrRNA genes was 341F (5 -CCTACGGGNGGCWGCAG-3 ) and 785R (5 -GACTACHVGGGTATCTAATCC-3 ) . The PCR program was as follows: 2 min at 95 C; 25 cycles of 30 s at 95 C, 30 s at 55 C, and 45 s at 72 C; and a final extension step at 72 C for 10 min.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3144110">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3144110</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08875357</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>JX-C1-B</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3908243" alias="JX-W2-B">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3908243</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3878188">JX-W2-B</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Rhizospheric bacterica of wild rice ( accompanied with weeds) in Jiangxi</TITLE>
    <STUDY_REF accession="SRP139050">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP139050</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA449026</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The primer pair used to amplify the V3-V4 hypervariable regions of the bacterial 16SrRNA genes was 341F (5 -CCTACGGGNGGCWGCAG-3 ) and 785R (5 -GACTACHVGGGTATCTAATCC-3 ) . The PCR program was as follows: 2 min at 95 C; 25 cycles of 30 s at 95 C, 30 s at 55 C, and 45 s at 72 C; and a final extension step at 72 C for 10 min.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3144111">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3144111</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08875360</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>JX-W2-B</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3908244" alias="JX-W1-F">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3908244</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3878188">JX-W1-F</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Rhizospheric fungi of wild rice in Jiangxi</TITLE>
    <STUDY_REF accession="SRP139050">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP139050</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA449026</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The primer pair used to amplify the fungal ITS region was ITS3F (5'-GATGAAGAACGYAGYRAA-3') and ITS4R (5'-TCCTCCGCTTATTGATATGC-3'). The PCR program was as follows: 2 min at 95 C; 25 cycles of 30 s at 95 C, 30 s at 55 C, and 45 s at 72 C; and a final extension step at 72 C for 10 min.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3144112">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3144112</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08875363</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>JX-W1-F</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3908245" alias="GD-W2-F">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3908245</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3878188">GD-W2-F</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Rhizospheric fungia of wild rice ( accompanied with weeds) in Guangdong</TITLE>
    <STUDY_REF accession="SRP139050">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP139050</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA449026</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The primer pair used to amplify the fungal ITS region was ITS3F (5'-GATGAAGAACGYAGYRAA-3') and ITS4R (5'-TCCTCCGCTTATTGATATGC-3'). The PCR program was as follows: 2 min at 95 C; 25 cycles of 30 s at 95 C, 30 s at 55 C, and 45 s at 72 C; and a final extension step at 72 C for 10 min.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3144114">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3144114</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08875370</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GD-W2-F</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3908246" alias="HN-W2-F">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3908246</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3878188">HN-W2-F</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Rhizospheric fungi of wild rice ( accompanied with weeds) in Hainan</TITLE>
    <STUDY_REF accession="SRP139050">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP139050</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA449026</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The primer pair used to amplify the fungal ITS region was ITS3F (5'-GATGAAGAACGYAGYRAA-3') and ITS4R (5'-TCCTCCGCTTATTGATATGC-3'). The PCR program was as follows: 2 min at 95 C; 25 cycles of 30 s at 95 C, 30 s at 55 C, and 45 s at 72 C; and a final extension step at 72 C for 10 min.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3144113">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3144113</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08875371</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>HN-W2-F</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3908247" alias="HN-C1-F">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3908247</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3878188">HN-C1-F</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Rhizospheric fungi of cultivated rice in Hainan</TITLE>
    <STUDY_REF accession="SRP139050">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP139050</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA449026</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The primer pair used to amplify the fungal ITS region was ITS3F (5'-GATGAAGAACGYAGYRAA-3') and ITS4R (5'-TCCTCCGCTTATTGATATGC-3'). The PCR program was as follows: 2 min at 95 C; 25 cycles of 30 s at 95 C, 30 s at 55 C, and 45 s at 72 C; and a final extension step at 72 C for 10 min.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3144115">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3144115</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08875368</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>HN-C1-F</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3908248" alias="JX-W2-F">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3908248</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3878188">JX-W2-F</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Rhizospheric fungi of wild rice ( accompanied with weeds) in Jiangxi</TITLE>
    <STUDY_REF accession="SRP139050">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP139050</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA449026</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The primer pair used to amplify the fungal ITS region was ITS3F (5'-GATGAAGAACGYAGYRAA-3') and ITS4R (5'-TCCTCCGCTTATTGATATGC-3'). The PCR program was as follows: 2 min at 95 C; 25 cycles of 30 s at 95 C, 30 s at 55 C, and 45 s at 72 C; and a final extension step at 72 C for 10 min.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3144116">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3144116</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08875369</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>JX-W2-F</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3908249" alias="JX-C1-F">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3908249</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3878188">JX-C1-F</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Rhizospheric fungi of cultivated rice in Jiangxi</TITLE>
    <STUDY_REF accession="SRP139050">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP139050</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA449026</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The primer pair used to amplify the fungal ITS region was ITS3F (5'-GATGAAGAACGYAGYRAA-3') and ITS4R (5'-TCCTCCGCTTATTGATATGC-3'). The PCR program was as follows: 2 min at 95 C; 25 cycles of 30 s at 95 C, 30 s at 55 C, and 45 s at 72 C; and a final extension step at 72 C for 10 min.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3144117">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3144117</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08875366</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>JX-C1-F</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3908250" alias="GD-C1-F">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3908250</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3878188">GD-C1-F</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Rhizospheric fungi of cultivatedrice in Guangdong</TITLE>
    <STUDY_REF accession="SRP139050">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP139050</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA449026</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The primer pair used to amplify the fungal ITS region was ITS3F (5'-GATGAAGAACGYAGYRAA-3') and ITS4R (5'-TCCTCCGCTTATTGATATGC-3'). The PCR program was as follows: 2 min at 95 C; 25 cycles of 30 s at 95 C, 30 s at 55 C, and 45 s at 72 C; and a final extension step at 72 C for 10 min.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3144118">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3144118</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08875367</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GD-C1-F</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3908251" alias="GD-W1-F">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3908251</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3878188">GD-W1-F</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Rhizospheric fungi of wild rice in Guangdong</TITLE>
    <STUDY_REF accession="SRP139050">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP139050</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA449026</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The primer pair used to amplify the fungal ITS region was ITS3F (5'-GATGAAGAACGYAGYRAA-3') and ITS4R (5'-TCCTCCGCTTATTGATATGC-3'). The PCR program was as follows: 2 min at 95 C; 25 cycles of 30 s at 95 C, 30 s at 55 C, and 45 s at 72 C; and a final extension step at 72 C for 10 min.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3144119">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3144119</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08875364</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GD-W1-F</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3908252" alias="HN-W1-F">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3908252</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3878188">HN-W1-F</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Rhizospheric fungi of wild rice in Hainan</TITLE>
    <STUDY_REF accession="SRP139050">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP139050</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA449026</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The primer pair used to amplify the fungal ITS region was ITS3F (5'-GATGAAGAACGYAGYRAA-3') and ITS4R (5'-TCCTCCGCTTATTGATATGC-3'). The PCR program was as follows: 2 min at 95 C; 25 cycles of 30 s at 95 C, 30 s at 55 C, and 45 s at 72 C; and a final extension step at 72 C for 10 min.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3144120">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3144120</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08875365</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>HN-W1-F</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3908253" alias="JX-W1-B">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3908253</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3878188">JX-W1-B</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Rhizospheric bacterica of wild rice in Jiangxi</TITLE>
    <STUDY_REF accession="SRP139050">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP139050</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA449026</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The primer pair used to amplify the V3-V4 hypervariable regions of the bacterial 16SrRNA genes was 341F (5 -CCTACGGGNGGCWGCAG-3 ) and 785R (5 -GACTACHVGGGTATCTAATCC-3 ) . The PCR program was as follows: 2 min at 95 C; 25 cycles of 30 s at 95 C, 30 s at 55 C, and 45 s at 72 C; and a final extension step at 72 C for 10 min.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3144121">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3144121</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08875354</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>JX-W1-B</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3908254" alias="HN-W2-B">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3908254</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3878188">HN-W2-B</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Rhizospheric bacterica of wild rice ( accompanied with weeds) in Hainan</TITLE>
    <STUDY_REF accession="SRP139050">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP139050</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA449026</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The primer pair used to amplify the V3-V4 hypervariable regions of the bacterial 16SrRNA genes was 341F (5 -CCTACGGGNGGCWGCAG-3 ) and 785R (5 -GACTACHVGGGTATCTAATCC-3 ) . The PCR program was as follows: 2 min at 95 C; 25 cycles of 30 s at 95 C, 30 s at 55 C, and 45 s at 72 C; and a final extension step at 72 C for 10 min.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3144122">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3144122</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08875362</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>HN-W2-B</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3908255" alias="GD-W2-B">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3908255</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3878188">GD-W2-B</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Rhizospheric bacterica of wild rice ( accompanied with weeds) in Guangdong</TITLE>
    <STUDY_REF accession="SRP139050">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP139050</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA449026</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The primer pair used to amplify the V3-V4 hypervariable regions of the bacterial 16SrRNA genes was 341F (5 -CCTACGGGNGGCWGCAG-3 ) and 785R (5 -GACTACHVGGGTATCTAATCC-3 ) . The PCR program was as follows: 2 min at 95 C; 25 cycles of 30 s at 95 C, 30 s at 55 C, and 45 s at 72 C; and a final extension step at 72 C for 10 min.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3144124">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3144124</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08875361</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GD-W2-B</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3908256" alias="GD-W1-B">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3908256</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3878188">GD-W1-B</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Rhizospheric bacterica of wild rice in Guangdong</TITLE>
    <STUDY_REF accession="SRP139050">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP139050</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA449026</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The primer pair used to amplify the V3-V4 hypervariable regions of the bacterial 16SrRNA genes was 341F (5 -CCTACGGGNGGCWGCAG-3 ) and 785R (5 -GACTACHVGGGTATCTAATCC-3 ) . The PCR program was as follows: 2 min at 95 C; 25 cycles of 30 s at 95 C, 30 s at 55 C, and 45 s at 72 C; and a final extension step at 72 C for 10 min.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3144123">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3144123</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08875355</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GD-W1-B</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
