<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX17293190" alias="GSM6513080_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17293190</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6513080_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6513080: CB-P4-mirna02; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP394555">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394555</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874432</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14857512">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14857512</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6513080</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6513080</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs from UCMSCs and CBMSCs at early (passage 4) and late (passage 11) passages were extracted with mirVana miRNA isolation kit (Life Technologies, Gaithersburg, MD, USA) according to the manufacturer's protocol. Ribo-zero kit for rRNA removal;One-stranded cDNA was synthesized using RNA as a template and six-base random primers; The second-stranded cDNA was synthesised by adding buffer, dNTPs and enzymes, followed by purification of the double-stranded cDNA using VAHTSTM DNA Clean Beads. purification of double-stranded cDNA;Accurate quantification of library concentrations with Qubit, determination of library fragment size distribution with Agilent 2100 Bioanalyzer</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ABI_SOLID>
        <INSTRUMENT_MODEL>AB SOLiD System</INSTRUMENT_MODEL>
      </ABI_SOLID>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17293191" alias="GSM6513081_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17293191</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6513081_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6513081: CB-P11-mirna04; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP394555">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394555</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874432</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14857513">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14857513</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6513081</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6513081</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs from UCMSCs and CBMSCs at early (passage 4) and late (passage 11) passages were extracted with mirVana miRNA isolation kit (Life Technologies, Gaithersburg, MD, USA) according to the manufacturer's protocol. Ribo-zero kit for rRNA removal;One-stranded cDNA was synthesized using RNA as a template and six-base random primers; The second-stranded cDNA was synthesised by adding buffer, dNTPs and enzymes, followed by purification of the double-stranded cDNA using VAHTSTM DNA Clean Beads. purification of double-stranded cDNA;Accurate quantification of library concentrations with Qubit, determination of library fragment size distribution with Agilent 2100 Bioanalyzer</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ABI_SOLID>
        <INSTRUMENT_MODEL>AB SOLiD System</INSTRUMENT_MODEL>
      </ABI_SOLID>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17293192" alias="GSM6513082_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17293192</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6513082_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6513082: UC-P4-mirna01; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP394555">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394555</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874432</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14857514">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14857514</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6513082</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6513082</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs from UCMSCs and CBMSCs at early (passage 4) and late (passage 11) passages were extracted with mirVana miRNA isolation kit (Life Technologies, Gaithersburg, MD, USA) according to the manufacturer's protocol. Ribo-zero kit for rRNA removal;One-stranded cDNA was synthesized using RNA as a template and six-base random primers; The second-stranded cDNA was synthesised by adding buffer, dNTPs and enzymes, followed by purification of the double-stranded cDNA using VAHTSTM DNA Clean Beads. purification of double-stranded cDNA;Accurate quantification of library concentrations with Qubit, determination of library fragment size distribution with Agilent 2100 Bioanalyzer</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ABI_SOLID>
        <INSTRUMENT_MODEL>AB SOLiD System</INSTRUMENT_MODEL>
      </ABI_SOLID>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17293193" alias="GSM6513083_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17293193</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6513083_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6513083: UC-P11-mirna03; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP394555">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394555</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874432</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14857515">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14857515</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6513083</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6513083</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs from UCMSCs and CBMSCs at early (passage 4) and late (passage 11) passages were extracted with mirVana miRNA isolation kit (Life Technologies, Gaithersburg, MD, USA) according to the manufacturer's protocol. Ribo-zero kit for rRNA removal;One-stranded cDNA was synthesized using RNA as a template and six-base random primers; The second-stranded cDNA was synthesised by adding buffer, dNTPs and enzymes, followed by purification of the double-stranded cDNA using VAHTSTM DNA Clean Beads. purification of double-stranded cDNA;Accurate quantification of library concentrations with Qubit, determination of library fragment size distribution with Agilent 2100 Bioanalyzer</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ABI_SOLID>
        <INSTRUMENT_MODEL>AB SOLiD System</INSTRUMENT_MODEL>
      </ABI_SOLID>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
