<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX11374843" alias="DC-N1_RNASeq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11374843</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9969593">DC-N1_RNASeq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of mouse lung DCs</TITLE>
    <STUDY_REF accession="SRP327385">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP327385</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9969593">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Flow cytometry-sorted cells were collected in RLT buffer (Qiagen; Hilden, Germany), and RNA was extracted and DNAse-treated using RNeasy Mini Kit (Qiagen) according to the manufacturers protocol. cDNA libraries were synthesized using Clontech SMARTer Stranded RNA-Seq kit (Mountain View, CA) with multiplexing primers. Quality of RNA and cDNA libraries were analyzed using 2100 BioAnalyzer (Agilent Technologies; Santa Clara, CA), then samples were sequenced with Illumina HiSeq2500 (San Diego, CA).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS9420816">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS9420816</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|imessaoudi">DC-N1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DC-N1_RNASeq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
