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    </IDENTIFIERS>
    <TITLE>metagenome of bee</TITLE>
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      <DESIGN_DESCRIPTION>Illumina RNAseq libraries were prepared with the TruSeq RNA Sample Prep kit (Illumina, San Diego, CA) per the manufacturers protocol, without the poly-A isolation steps. Adapters containing six nucleotide indexes were ligated to the double-stranded cDNA. The DNA was purified between enzymatic reactions and the size selection of the library was performed with AMPure XT beads (Beckman Coulter Genomics, Danvers, MA). Libraries are assessed for concentration and fragment size using the DNA High Sensitivity Assay on the LabChip GX (Perkin Elmer, Waltham, MA)</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX17898245</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12130002">healthy_bee_1_fastq2</SUBMITTER_ID>
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    <TITLE>metagenome of bee</TITLE>
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    <TITLE>metagenome of bee</TITLE>
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      <DESIGN_DESCRIPTION>Illumina RNAseq libraries were prepared with the TruSeq RNA Sample Prep kit (Illumina, San Diego, CA) per the manufacturers protocol, without the poly-A isolation steps. Adapters containing six nucleotide indexes were ligated to the double-stranded cDNA. The DNA was purified between enzymatic reactions and the size selection of the library was performed with AMPure XT beads (Beckman Coulter Genomics, Danvers, MA). Libraries are assessed for concentration and fragment size using the DNA High Sensitivity Assay on the LabChip GX (Perkin Elmer, Waltham, MA)</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX17898247</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12130002">diseased_bee_6_fastq2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>metagenome of bee</TITLE>
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        <PRIMARY_ID>SRP402742</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12130002">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
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      <DESIGN_DESCRIPTION>Illumina RNAseq libraries were prepared with the TruSeq RNA Sample Prep kit (Illumina, San Diego, CA) per the manufacturers protocol, without the poly-A isolation steps. Adapters containing six nucleotide indexes were ligated to the double-stranded cDNA. The DNA was purified between enzymatic reactions and the size selection of the library was performed with AMPure XT beads (Beckman Coulter Genomics, Danvers, MA). Libraries are assessed for concentration and fragment size using the DNA High Sensitivity Assay on the LabChip GX (Perkin Elmer, Waltham, MA)</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX17898248</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12130002">healthy_bee_2_fastq1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>metagenome of bee</TITLE>
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        <PRIMARY_ID>SRP402742</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12130002">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
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      <DESIGN_DESCRIPTION>Illumina RNAseq libraries were prepared with the TruSeq RNA Sample Prep kit (Illumina, San Diego, CA) per the manufacturers protocol, without the poly-A isolation steps. Adapters containing six nucleotide indexes were ligated to the double-stranded cDNA. The DNA was purified between enzymatic reactions and the size selection of the library was performed with AMPure XT beads (Beckman Coulter Genomics, Danvers, MA). Libraries are assessed for concentration and fragment size using the DNA High Sensitivity Assay on the LabChip GX (Perkin Elmer, Waltham, MA)</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS15415119</PRIMARY_ID>
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        <LIBRARY_NAME>healthy_bee_2_fastq1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
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        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
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          <SINGLE/>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX17898249</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12130002">healthy_bee_2_fastq2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>metagenome of bee</TITLE>
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        <PRIMARY_ID>SRP402742</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>Illumina RNAseq libraries were prepared with the TruSeq RNA Sample Prep kit (Illumina, San Diego, CA) per the manufacturers protocol, without the poly-A isolation steps. Adapters containing six nucleotide indexes were ligated to the double-stranded cDNA. The DNA was purified between enzymatic reactions and the size selection of the library was performed with AMPure XT beads (Beckman Coulter Genomics, Danvers, MA). Libraries are assessed for concentration and fragment size using the DNA High Sensitivity Assay on the LabChip GX (Perkin Elmer, Waltham, MA)</DESIGN_DESCRIPTION>
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        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
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          <SINGLE/>
        </LIBRARY_LAYOUT>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX17898250</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12130002">healthy_bee_3_fastq1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>metagenome of bee</TITLE>
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        <SUBMITTER_ID namespace="SUB12130002">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina RNAseq libraries were prepared with the TruSeq RNA Sample Prep kit (Illumina, San Diego, CA) per the manufacturers protocol, without the poly-A isolation steps. Adapters containing six nucleotide indexes were ligated to the double-stranded cDNA. The DNA was purified between enzymatic reactions and the size selection of the library was performed with AMPure XT beads (Beckman Coulter Genomics, Danvers, MA). Libraries are assessed for concentration and fragment size using the DNA High Sensitivity Assay on the LabChip GX (Perkin Elmer, Waltham, MA)</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS15415120</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|yahuigao306@gmail.com">healthy_bee_3</SUBMITTER_ID>
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        <LIBRARY_NAME>healthy_bee_3_fastq1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
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        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX17898251</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12130002">healthy_bee_3_fastq2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>metagenome of bee</TITLE>
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        <PRIMARY_ID>SRP402742</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12130002">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
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      <DESIGN_DESCRIPTION>Illumina RNAseq libraries were prepared with the TruSeq RNA Sample Prep kit (Illumina, San Diego, CA) per the manufacturers protocol, without the poly-A isolation steps. Adapters containing six nucleotide indexes were ligated to the double-stranded cDNA. The DNA was purified between enzymatic reactions and the size selection of the library was performed with AMPure XT beads (Beckman Coulter Genomics, Danvers, MA). Libraries are assessed for concentration and fragment size using the DNA High Sensitivity Assay on the LabChip GX (Perkin Elmer, Waltham, MA)</DESIGN_DESCRIPTION>
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        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
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        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX17898252</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12130002">diseased_bee_1_fastq1</SUBMITTER_ID>
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    <TITLE>metagenome of bee</TITLE>
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      <DESIGN_DESCRIPTION>Illumina RNAseq libraries were prepared with the TruSeq RNA Sample Prep kit (Illumina, San Diego, CA) per the manufacturers protocol, without the poly-A isolation steps. Adapters containing six nucleotide indexes were ligated to the double-stranded cDNA. The DNA was purified between enzymatic reactions and the size selection of the library was performed with AMPure XT beads (Beckman Coulter Genomics, Danvers, MA). Libraries are assessed for concentration and fragment size using the DNA High Sensitivity Assay on the LabChip GX (Perkin Elmer, Waltham, MA)</DESIGN_DESCRIPTION>
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      <LIBRARY_DESCRIPTOR>
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        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
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        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
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          <SINGLE/>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX17898253</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12130002">diseased_bee_1_fastq2</SUBMITTER_ID>
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    <TITLE>metagenome of bee</TITLE>
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      <DESIGN_DESCRIPTION>Illumina RNAseq libraries were prepared with the TruSeq RNA Sample Prep kit (Illumina, San Diego, CA) per the manufacturers protocol, without the poly-A isolation steps. Adapters containing six nucleotide indexes were ligated to the double-stranded cDNA. The DNA was purified between enzymatic reactions and the size selection of the library was performed with AMPure XT beads (Beckman Coulter Genomics, Danvers, MA). Libraries are assessed for concentration and fragment size using the DNA High Sensitivity Assay on the LabChip GX (Perkin Elmer, Waltham, MA)</DESIGN_DESCRIPTION>
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      <LIBRARY_DESCRIPTOR>
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        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
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          <SINGLE/>
        </LIBRARY_LAYOUT>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
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  </EXPERIMENT>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX17898254</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12130002">diseased_bee_2_fastq1</SUBMITTER_ID>
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    <TITLE>metagenome of bee</TITLE>
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      </IDENTIFIERS>
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      <DESIGN_DESCRIPTION>Illumina RNAseq libraries were prepared with the TruSeq RNA Sample Prep kit (Illumina, San Diego, CA) per the manufacturers protocol, without the poly-A isolation steps. Adapters containing six nucleotide indexes were ligated to the double-stranded cDNA. The DNA was purified between enzymatic reactions and the size selection of the library was performed with AMPure XT beads (Beckman Coulter Genomics, Danvers, MA). Libraries are assessed for concentration and fragment size using the DNA High Sensitivity Assay on the LabChip GX (Perkin Elmer, Waltham, MA)</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS15415122</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|yahuigao306@gmail.com">diseased_bee_2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>diseased_bee_2_fastq1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX17898255</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12130002">diseased_bee_2_fastq2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>metagenome of bee</TITLE>
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      </IDENTIFIERS>
    </STUDY_REF>
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      <DESIGN_DESCRIPTION>Illumina RNAseq libraries were prepared with the TruSeq RNA Sample Prep kit (Illumina, San Diego, CA) per the manufacturers protocol, without the poly-A isolation steps. Adapters containing six nucleotide indexes were ligated to the double-stranded cDNA. The DNA was purified between enzymatic reactions and the size selection of the library was performed with AMPure XT beads (Beckman Coulter Genomics, Danvers, MA). Libraries are assessed for concentration and fragment size using the DNA High Sensitivity Assay on the LabChip GX (Perkin Elmer, Waltham, MA)</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS15415122</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|yahuigao306@gmail.com">diseased_bee_2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>diseased_bee_2_fastq2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
