<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX15212864" alias="GSM6124422_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15212864</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6124422_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6124422: N1 for sncRNA-seq; Homo sapiens; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP374372">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374372</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA836563</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12950470">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12950470</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6124422</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6124422</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>For small RNA-seq profiling, the plasma exosome RNA was purified from 13 subjects, respectively. The exosome RNA was isolated from plasma exosome using the RNA isolation reagent TRIzol (Invitrogen). By using the QIAseq® miRNA Library Kit (QIAgen, Cat# 331505), small RNA-seq libraries were constructed with 2~10 ng of the prepared exosomal small RNA in line with the manufacturer's protocols. Small RNA-seq libraries were prepared according to Illumina's instructions and sequenced on an Illumina 3000 analyzer by EPIBIOTEK Company (Guangzhou, China).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15212865" alias="GSM6124423_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15212865</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6124423_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6124423: N2 for sncRNA-seq; Homo sapiens; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP374372">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374372</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA836563</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12950471">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12950471</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6124423</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6124423</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>For small RNA-seq profiling, the plasma exosome RNA was purified from 13 subjects, respectively. The exosome RNA was isolated from plasma exosome using the RNA isolation reagent TRIzol (Invitrogen). By using the QIAseq® miRNA Library Kit (QIAgen, Cat# 331505), small RNA-seq libraries were constructed with 2~10 ng of the prepared exosomal small RNA in line with the manufacturer's protocols. Small RNA-seq libraries were prepared according to Illumina's instructions and sequenced on an Illumina 3000 analyzer by EPIBIOTEK Company (Guangzhou, China).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15212866" alias="GSM6124424_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15212866</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6124424_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6124424: N3 for sncRNA-seq; Homo sapiens; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP374372">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374372</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA836563</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12950472">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12950472</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6124424</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6124424</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>For small RNA-seq profiling, the plasma exosome RNA was purified from 13 subjects, respectively. The exosome RNA was isolated from plasma exosome using the RNA isolation reagent TRIzol (Invitrogen). By using the QIAseq® miRNA Library Kit (QIAgen, Cat# 331505), small RNA-seq libraries were constructed with 2~10 ng of the prepared exosomal small RNA in line with the manufacturer's protocols. Small RNA-seq libraries were prepared according to Illumina's instructions and sequenced on an Illumina 3000 analyzer by EPIBIOTEK Company (Guangzhou, China).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15212867" alias="GSM6124425_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15212867</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6124425_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6124425: H1 for sncRNA-seq; Homo sapiens; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP374372">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374372</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA836563</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12950473">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12950473</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6124425</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6124425</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>For small RNA-seq profiling, the plasma exosome RNA was purified from 13 subjects, respectively. The exosome RNA was isolated from plasma exosome using the RNA isolation reagent TRIzol (Invitrogen). By using the QIAseq® miRNA Library Kit (QIAgen, Cat# 331505), small RNA-seq libraries were constructed with 2~10 ng of the prepared exosomal small RNA in line with the manufacturer's protocols. Small RNA-seq libraries were prepared according to Illumina's instructions and sequenced on an Illumina 3000 analyzer by EPIBIOTEK Company (Guangzhou, China).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15212868" alias="GSM6124426_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15212868</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6124426_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6124426: H2 for sncRNA-seq; Homo sapiens; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP374372">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374372</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA836563</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12950474">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12950474</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6124426</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6124426</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>For small RNA-seq profiling, the plasma exosome RNA was purified from 13 subjects, respectively. The exosome RNA was isolated from plasma exosome using the RNA isolation reagent TRIzol (Invitrogen). By using the QIAseq® miRNA Library Kit (QIAgen, Cat# 331505), small RNA-seq libraries were constructed with 2~10 ng of the prepared exosomal small RNA in line with the manufacturer's protocols. Small RNA-seq libraries were prepared according to Illumina's instructions and sequenced on an Illumina 3000 analyzer by EPIBIOTEK Company (Guangzhou, China).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15212869" alias="GSM6124427_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15212869</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6124427_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6124427: H3 for sncRNA-seq; Homo sapiens; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP374372">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374372</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA836563</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12950475">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12950475</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6124427</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6124427</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>For small RNA-seq profiling, the plasma exosome RNA was purified from 13 subjects, respectively. The exosome RNA was isolated from plasma exosome using the RNA isolation reagent TRIzol (Invitrogen). By using the QIAseq® miRNA Library Kit (QIAgen, Cat# 331505), small RNA-seq libraries were constructed with 2~10 ng of the prepared exosomal small RNA in line with the manufacturer's protocols. Small RNA-seq libraries were prepared according to Illumina's instructions and sequenced on an Illumina 3000 analyzer by EPIBIOTEK Company (Guangzhou, China).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15212870" alias="GSM6124428_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15212870</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6124428_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6124428: H4 for sncRNA-seq; Homo sapiens; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP374372">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374372</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA836563</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12950476">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12950476</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6124428</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6124428</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>For small RNA-seq profiling, the plasma exosome RNA was purified from 13 subjects, respectively. The exosome RNA was isolated from plasma exosome using the RNA isolation reagent TRIzol (Invitrogen). By using the QIAseq® miRNA Library Kit (QIAgen, Cat# 331505), small RNA-seq libraries were constructed with 2~10 ng of the prepared exosomal small RNA in line with the manufacturer's protocols. Small RNA-seq libraries were prepared according to Illumina's instructions and sequenced on an Illumina 3000 analyzer by EPIBIOTEK Company (Guangzhou, China).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15212871" alias="GSM6124429_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15212871</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6124429_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6124429: L1 for sncRNA-seq; Homo sapiens; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP374372">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374372</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA836563</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12950477">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12950477</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6124429</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6124429</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>For small RNA-seq profiling, the plasma exosome RNA was purified from 13 subjects, respectively. The exosome RNA was isolated from plasma exosome using the RNA isolation reagent TRIzol (Invitrogen). By using the QIAseq® miRNA Library Kit (QIAgen, Cat# 331505), small RNA-seq libraries were constructed with 2~10 ng of the prepared exosomal small RNA in line with the manufacturer's protocols. Small RNA-seq libraries were prepared according to Illumina's instructions and sequenced on an Illumina 3000 analyzer by EPIBIOTEK Company (Guangzhou, China).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15212872" alias="GSM6124430_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15212872</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6124430_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6124430: L2 for sncRNA-seq; Homo sapiens; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP374372">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374372</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA836563</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12950478">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12950478</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6124430</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6124430</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>For small RNA-seq profiling, the plasma exosome RNA was purified from 13 subjects, respectively. The exosome RNA was isolated from plasma exosome using the RNA isolation reagent TRIzol (Invitrogen). By using the QIAseq® miRNA Library Kit (QIAgen, Cat# 331505), small RNA-seq libraries were constructed with 2~10 ng of the prepared exosomal small RNA in line with the manufacturer's protocols. Small RNA-seq libraries were prepared according to Illumina's instructions and sequenced on an Illumina 3000 analyzer by EPIBIOTEK Company (Guangzhou, China).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15212873" alias="GSM6124431_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15212873</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6124431_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6124431: L3 for sncRNA-seq; Homo sapiens; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP374372">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374372</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA836563</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12950479">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12950479</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6124431</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6124431</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>For small RNA-seq profiling, the plasma exosome RNA was purified from 13 subjects, respectively. The exosome RNA was isolated from plasma exosome using the RNA isolation reagent TRIzol (Invitrogen). By using the QIAseq® miRNA Library Kit (QIAgen, Cat# 331505), small RNA-seq libraries were constructed with 2~10 ng of the prepared exosomal small RNA in line with the manufacturer's protocols. Small RNA-seq libraries were prepared according to Illumina's instructions and sequenced on an Illumina 3000 analyzer by EPIBIOTEK Company (Guangzhou, China).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15212874" alias="GSM6124432_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15212874</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6124432_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6124432: L4 for sncRNA-seq; Homo sapiens; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP374372">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374372</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA836563</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12950480">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12950480</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6124432</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6124432</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>For small RNA-seq profiling, the plasma exosome RNA was purified from 13 subjects, respectively. The exosome RNA was isolated from plasma exosome using the RNA isolation reagent TRIzol (Invitrogen). By using the QIAseq® miRNA Library Kit (QIAgen, Cat# 331505), small RNA-seq libraries were constructed with 2~10 ng of the prepared exosomal small RNA in line with the manufacturer's protocols. Small RNA-seq libraries were prepared according to Illumina's instructions and sequenced on an Illumina 3000 analyzer by EPIBIOTEK Company (Guangzhou, China).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15212875" alias="GSM6124433_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15212875</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6124433_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6124433: L5 for sncRNA-seq; Homo sapiens; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP374372">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374372</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA836563</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12950481">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12950481</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6124433</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6124433</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>For small RNA-seq profiling, the plasma exosome RNA was purified from 13 subjects, respectively. The exosome RNA was isolated from plasma exosome using the RNA isolation reagent TRIzol (Invitrogen). By using the QIAseq® miRNA Library Kit (QIAgen, Cat# 331505), small RNA-seq libraries were constructed with 2~10 ng of the prepared exosomal small RNA in line with the manufacturer's protocols. Small RNA-seq libraries were prepared according to Illumina's instructions and sequenced on an Illumina 3000 analyzer by EPIBIOTEK Company (Guangzhou, China).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15212876" alias="GSM6124434_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15212876</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6124434_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6124434: L6 for sncRNA-seq; Homo sapiens; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP374372">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374372</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA836563</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12950482">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12950482</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6124434</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6124434</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>For small RNA-seq profiling, the plasma exosome RNA was purified from 13 subjects, respectively. The exosome RNA was isolated from plasma exosome using the RNA isolation reagent TRIzol (Invitrogen). By using the QIAseq® miRNA Library Kit (QIAgen, Cat# 331505), small RNA-seq libraries were constructed with 2~10 ng of the prepared exosomal small RNA in line with the manufacturer's protocols. Small RNA-seq libraries were prepared according to Illumina's instructions and sequenced on an Illumina 3000 analyzer by EPIBIOTEK Company (Guangzhou, China).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
