<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX15214923" alias="GSM6124786_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15214923</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6124786_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6124786: RNA_Hoxb8FL_cDC_1_S4; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP374423">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374423</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA836605</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12952240">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12952240</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6124786</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6124786</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hoxb8-FL cells were sorted as described in the manuscript and RNA was isolated using RNeasy mini kit (QIAGEN) and QIAshredder homogenizer (QIAGEN) according to the manufacturer's instructions. 1 ng of total RNA was used for the construction of sequencing libraries. Libraries were prepared for sequencing using standard Illumina protocols and Low input Clontech SMART-Seq HT with Nxt HT following manufacturer's protocols.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15214928" alias="GSM6124791_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15214928</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6124791_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6124791: RNA_Hoxb8FL_cDC_2_S9; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP374423">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374423</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA836605</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12952245">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12952245</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6124791</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6124791</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hoxb8-FL cells were sorted as described in the manuscript and RNA was isolated using RNeasy mini kit (QIAGEN) and QIAshredder homogenizer (QIAGEN) according to the manufacturer's instructions. 1 ng of total RNA was used for the construction of sequencing libraries. Libraries were prepared for sequencing using standard Illumina protocols and Low input Clontech SMART-Seq HT with Nxt HT following manufacturer's protocols.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15214933" alias="GSM6124796_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15214933</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6124796_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6124796: RNA_Hoxb8FL_cDC_3_S14; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP374423">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374423</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA836605</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12952250">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12952250</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6124796</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6124796</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hoxb8-FL cells were sorted as described in the manuscript and RNA was isolated using RNeasy mini kit (QIAGEN) and QIAshredder homogenizer (QIAGEN) according to the manufacturer's instructions. 1 ng of total RNA was used for the construction of sequencing libraries. Libraries were prepared for sequencing using standard Illumina protocols and Low input Clontech SMART-Seq HT with Nxt HT following manufacturer's protocols.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
