<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="GSM4104717" accession="SRX6935570">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935570</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4104717</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4104717: LT-HSCs , Ccp3_WT; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223947" refname="GSE138298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223947</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5465579">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465579</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4104717</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>LT-HSCs were sorted by flow cytometry. Total RNAs were extracted with an RNA Miniprep Kit (Tiangen, Beijing, China) according to the manufacturer's protocol. 0.5 ug of total RNA were qualified using Agilent 2100 for the construction of sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <BGISEQ>
        <INSTRUMENT_MODEL>BGISEQ-500</INSTRUMENT_MODEL>
      </BGISEQ>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>304104717</ID>
          <LABEL>GSM4104717</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4104717</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4104718" accession="SRX6935571">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935571</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4104718</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4104718: LT-HSCs , Ccp3_KO; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223947" refname="GSE138298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223947</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5465580">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465580</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4104718</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>LT-HSCs were sorted by flow cytometry. Total RNAs were extracted with an RNA Miniprep Kit (Tiangen, Beijing, China) according to the manufacturer's protocol. 0.5 ug of total RNA were qualified using Agilent 2100 for the construction of sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <BGISEQ>
        <INSTRUMENT_MODEL>BGISEQ-500</INSTRUMENT_MODEL>
      </BGISEQ>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>304104718</ID>
          <LABEL>GSM4104718</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4104718</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
</EXPERIMENT_SET>
