<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX3641151" alias="PC-1 exosomal miRNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3641151</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3599869">PC-1 exosomal miRNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>exosomal miRNA of PC-1 pancreatic cancer cell</TITLE>
    <STUDY_REF accession="SRP132011">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP132011</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB3599869">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples of PC-1.0 exosomes and PC-1 exosomes were prepared for high-throughput sequencing. In brief, total RNA of each sample was extracted using TRIzol  Reagent (invitrogen) and then 2 libraries were constructed using smRNA-seq(for illumina) (clontech, CA, USA) according to the manufacturer's instruction. RNA-seq was performed using illumina HiSeqTM 2500(Illumina, Inc., San Diego, CA, USA). Raw data was processed to identified differentially expressed miRNAs(DEMs). DEM data was assigned for further bioinformatic analysis.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2907351">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2907351</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|wumengwei">PC-1 pancreatic cancer cell exosomal miRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PC-1 exosomal miRNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</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="SRX3641152" alias="PC-1.0 exosomal miRNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3641152</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3599869">PC-1.0 exosomal miRNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>exosomal miRNA of PC-1.0 pancreatic cancer cell</TITLE>
    <STUDY_REF accession="SRP132011">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP132011</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB3599869">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Samples of PC-1.0 exosomes and PC-1 exosomes were prepared for high-throughput sequencing. In brief, total RNA of each sample was extracted using TRIzol  Reagent (invitrogen) and then 2 libraries were constructed using smRNA-seq(for illumina) (clontech, CA, USA) according to the manufacturer's instruction. RNA-seq was performed using illumina HiSeqTM 2500(Illumina, Inc., San Diego, CA, USA). Raw data was processed to identified differentially expressed miRNAs(DEMs). DEM data was assigned for further bioinformatic analysis.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2907350">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2907350</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|wumengwei">PC-1.0 pancreatic cancer cell exosomal miRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PC-1.0 exosomal miRNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</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>
