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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX17232228" alias="GSM6510099_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17232228</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6510099_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6510099: T0_Naïve3; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP394178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874089</EXTERNAL_ID>
      </IDENTIFIERS>
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    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14798544">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14798544</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6510099</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6510099</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Fresh right lungs were immediately collected in RNAlater™ (Sigma, USA) for the next homogenization in QIAzol® Lysis Reagent (QIAGEN, Netherlands) with gentleMACS™ Dissociator (Miltenyi Biotec, Germany). RNA was extracted using the QIAcube robotic workstation with the miRNeasy Mini Kit (QIAGEN, Netherlands), including DNase digestion protocol. Libraries for massive parallel RNA sequencing (RNA-seq) were prepared with the QuantSeq 3' mRNA-Seq Library Prep Kit FWD (Lexogen) and sequenced, in two runs, with the use of an Illumina NextSeq500 platform, which generated at least 30 million reads/sample (75 bp Single End).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17232229" alias="GSM6510100_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17232229</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6510100_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6510100: T0_Naïve6; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP394178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874089</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14798545">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14798545</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6510100</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6510100</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Fresh right lungs were immediately collected in RNAlater™ (Sigma, USA) for the next homogenization in QIAzol® Lysis Reagent (QIAGEN, Netherlands) with gentleMACS™ Dissociator (Miltenyi Biotec, Germany). RNA was extracted using the QIAcube robotic workstation with the miRNeasy Mini Kit (QIAGEN, Netherlands), including DNase digestion protocol. Libraries for massive parallel RNA sequencing (RNA-seq) were prepared with the QuantSeq 3' mRNA-Seq Library Prep Kit FWD (Lexogen) and sequenced, in two runs, with the use of an Illumina NextSeq500 platform, which generated at least 30 million reads/sample (75 bp Single End).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17232230" alias="GSM6510101_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17232230</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6510101_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6510101: T07_Blm6; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP394178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874089</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14798546">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14798546</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6510101</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6510101</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Fresh right lungs were immediately collected in RNAlater™ (Sigma, USA) for the next homogenization in QIAzol® Lysis Reagent (QIAGEN, Netherlands) with gentleMACS™ Dissociator (Miltenyi Biotec, Germany). RNA was extracted using the QIAcube robotic workstation with the miRNeasy Mini Kit (QIAGEN, Netherlands), including DNase digestion protocol. Libraries for massive parallel RNA sequencing (RNA-seq) were prepared with the QuantSeq 3' mRNA-Seq Library Prep Kit FWD (Lexogen) and sequenced, in two runs, with the use of an Illumina NextSeq500 platform, which generated at least 30 million reads/sample (75 bp Single End).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17232231" alias="GSM6510102_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17232231</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6510102_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6510102: T07_Blm8; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP394178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874089</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14798547">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14798547</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6510102</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6510102</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Fresh right lungs were immediately collected in RNAlater™ (Sigma, USA) for the next homogenization in QIAzol® Lysis Reagent (QIAGEN, Netherlands) with gentleMACS™ Dissociator (Miltenyi Biotec, Germany). RNA was extracted using the QIAcube robotic workstation with the miRNeasy Mini Kit (QIAGEN, Netherlands), including DNase digestion protocol. Libraries for massive parallel RNA sequencing (RNA-seq) were prepared with the QuantSeq 3' mRNA-Seq Library Prep Kit FWD (Lexogen) and sequenced, in two runs, with the use of an Illumina NextSeq500 platform, which generated at least 30 million reads/sample (75 bp Single End).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17232232" alias="GSM6510103_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17232232</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6510103_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6510103: T07_Sal5; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP394178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874089</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14798548">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14798548</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6510103</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6510103</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Fresh right lungs were immediately collected in RNAlater™ (Sigma, USA) for the next homogenization in QIAzol® Lysis Reagent (QIAGEN, Netherlands) with gentleMACS™ Dissociator (Miltenyi Biotec, Germany). RNA was extracted using the QIAcube robotic workstation with the miRNeasy Mini Kit (QIAGEN, Netherlands), including DNase digestion protocol. Libraries for massive parallel RNA sequencing (RNA-seq) were prepared with the QuantSeq 3' mRNA-Seq Library Prep Kit FWD (Lexogen) and sequenced, in two runs, with the use of an Illumina NextSeq500 platform, which generated at least 30 million reads/sample (75 bp Single End).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17232233" alias="GSM6510104_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17232233</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6510104_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6510104: T07_Sal8; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP394178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874089</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14798549">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14798549</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6510104</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6510104</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Fresh right lungs were immediately collected in RNAlater™ (Sigma, USA) for the next homogenization in QIAzol® Lysis Reagent (QIAGEN, Netherlands) with gentleMACS™ Dissociator (Miltenyi Biotec, Germany). RNA was extracted using the QIAcube robotic workstation with the miRNeasy Mini Kit (QIAGEN, Netherlands), including DNase digestion protocol. Libraries for massive parallel RNA sequencing (RNA-seq) were prepared with the QuantSeq 3' mRNA-Seq Library Prep Kit FWD (Lexogen) and sequenced, in two runs, with the use of an Illumina NextSeq500 platform, which generated at least 30 million reads/sample (75 bp Single End).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17232234" alias="GSM6510105_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17232234</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6510105_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6510105: T14_Blm5; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP394178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874089</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14798550">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14798550</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6510105</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6510105</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Fresh right lungs were immediately collected in RNAlater™ (Sigma, USA) for the next homogenization in QIAzol® Lysis Reagent (QIAGEN, Netherlands) with gentleMACS™ Dissociator (Miltenyi Biotec, Germany). RNA was extracted using the QIAcube robotic workstation with the miRNeasy Mini Kit (QIAGEN, Netherlands), including DNase digestion protocol. Libraries for massive parallel RNA sequencing (RNA-seq) were prepared with the QuantSeq 3' mRNA-Seq Library Prep Kit FWD (Lexogen) and sequenced, in two runs, with the use of an Illumina NextSeq500 platform, which generated at least 30 million reads/sample (75 bp Single End).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17232235" alias="GSM6510106_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17232235</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6510106_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6510106: T14_Blm6; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP394178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874089</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14798551">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14798551</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6510106</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6510106</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Fresh right lungs were immediately collected in RNAlater™ (Sigma, USA) for the next homogenization in QIAzol® Lysis Reagent (QIAGEN, Netherlands) with gentleMACS™ Dissociator (Miltenyi Biotec, Germany). RNA was extracted using the QIAcube robotic workstation with the miRNeasy Mini Kit (QIAGEN, Netherlands), including DNase digestion protocol. Libraries for massive parallel RNA sequencing (RNA-seq) were prepared with the QuantSeq 3' mRNA-Seq Library Prep Kit FWD (Lexogen) and sequenced, in two runs, with the use of an Illumina NextSeq500 platform, which generated at least 30 million reads/sample (75 bp Single End).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17232236" alias="GSM6510107_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17232236</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6510107_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6510107: T14_Sal7; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP394178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874089</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14798552">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14798552</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6510107</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6510107</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Fresh right lungs were immediately collected in RNAlater™ (Sigma, USA) for the next homogenization in QIAzol® Lysis Reagent (QIAGEN, Netherlands) with gentleMACS™ Dissociator (Miltenyi Biotec, Germany). RNA was extracted using the QIAcube robotic workstation with the miRNeasy Mini Kit (QIAGEN, Netherlands), including DNase digestion protocol. Libraries for massive parallel RNA sequencing (RNA-seq) were prepared with the QuantSeq 3' mRNA-Seq Library Prep Kit FWD (Lexogen) and sequenced, in two runs, with the use of an Illumina NextSeq500 platform, which generated at least 30 million reads/sample (75 bp Single End).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17232237" alias="GSM6510108_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17232237</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6510108_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6510108: T14_Sal8; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP394178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874089</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14798553">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14798553</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6510108</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6510108</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Fresh right lungs were immediately collected in RNAlater™ (Sigma, USA) for the next homogenization in QIAzol® Lysis Reagent (QIAGEN, Netherlands) with gentleMACS™ Dissociator (Miltenyi Biotec, Germany). RNA was extracted using the QIAcube robotic workstation with the miRNeasy Mini Kit (QIAGEN, Netherlands), including DNase digestion protocol. Libraries for massive parallel RNA sequencing (RNA-seq) were prepared with the QuantSeq 3' mRNA-Seq Library Prep Kit FWD (Lexogen) and sequenced, in two runs, with the use of an Illumina NextSeq500 platform, which generated at least 30 million reads/sample (75 bp Single End).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17232238" alias="GSM6510109_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17232238</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6510109_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6510109: T21_Blm7; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP394178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874089</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14798554">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14798554</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6510109</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6510109</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Fresh right lungs were immediately collected in RNAlater™ (Sigma, USA) for the next homogenization in QIAzol® Lysis Reagent (QIAGEN, Netherlands) with gentleMACS™ Dissociator (Miltenyi Biotec, Germany). RNA was extracted using the QIAcube robotic workstation with the miRNeasy Mini Kit (QIAGEN, Netherlands), including DNase digestion protocol. Libraries for massive parallel RNA sequencing (RNA-seq) were prepared with the QuantSeq 3' mRNA-Seq Library Prep Kit FWD (Lexogen) and sequenced, in two runs, with the use of an Illumina NextSeq500 platform, which generated at least 30 million reads/sample (75 bp Single End).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17232239" alias="GSM6510110_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17232239</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6510110_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6510110: T21_Sal5; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP394178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874089</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14798555">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14798555</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6510110</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6510110</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Fresh right lungs were immediately collected in RNAlater™ (Sigma, USA) for the next homogenization in QIAzol® Lysis Reagent (QIAGEN, Netherlands) with gentleMACS™ Dissociator (Miltenyi Biotec, Germany). RNA was extracted using the QIAcube robotic workstation with the miRNeasy Mini Kit (QIAGEN, Netherlands), including DNase digestion protocol. Libraries for massive parallel RNA sequencing (RNA-seq) were prepared with the QuantSeq 3' mRNA-Seq Library Prep Kit FWD (Lexogen) and sequenced, in two runs, with the use of an Illumina NextSeq500 platform, which generated at least 30 million reads/sample (75 bp Single End).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17232240" alias="GSM6510111_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17232240</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6510111_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6510111: T21_Sal8; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP394178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874089</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14798556">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14798556</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6510111</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6510111</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Fresh right lungs were immediately collected in RNAlater™ (Sigma, USA) for the next homogenization in QIAzol® Lysis Reagent (QIAGEN, Netherlands) with gentleMACS™ Dissociator (Miltenyi Biotec, Germany). RNA was extracted using the QIAcube robotic workstation with the miRNeasy Mini Kit (QIAGEN, Netherlands), including DNase digestion protocol. Libraries for massive parallel RNA sequencing (RNA-seq) were prepared with the QuantSeq 3' mRNA-Seq Library Prep Kit FWD (Lexogen) and sequenced, in two runs, with the use of an Illumina NextSeq500 platform, which generated at least 30 million reads/sample (75 bp Single End).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17232241" alias="GSM6510112_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17232241</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6510112_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6510112: T28_Blm5; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP394178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874089</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14798557">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14798557</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6510112</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6510112</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Fresh right lungs were immediately collected in RNAlater™ (Sigma, USA) for the next homogenization in QIAzol® Lysis Reagent (QIAGEN, Netherlands) with gentleMACS™ Dissociator (Miltenyi Biotec, Germany). RNA was extracted using the QIAcube robotic workstation with the miRNeasy Mini Kit (QIAGEN, Netherlands), including DNase digestion protocol. Libraries for massive parallel RNA sequencing (RNA-seq) were prepared with the QuantSeq 3' mRNA-Seq Library Prep Kit FWD (Lexogen) and sequenced, in two runs, with the use of an Illumina NextSeq500 platform, which generated at least 30 million reads/sample (75 bp Single End).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17232242" alias="GSM6510113_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17232242</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6510113_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6510113: T28_Blm7; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP394178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874089</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14798558">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14798558</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6510113</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6510113</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Fresh right lungs were immediately collected in RNAlater™ (Sigma, USA) for the next homogenization in QIAzol® Lysis Reagent (QIAGEN, Netherlands) with gentleMACS™ Dissociator (Miltenyi Biotec, Germany). RNA was extracted using the QIAcube robotic workstation with the miRNeasy Mini Kit (QIAGEN, Netherlands), including DNase digestion protocol. Libraries for massive parallel RNA sequencing (RNA-seq) were prepared with the QuantSeq 3' mRNA-Seq Library Prep Kit FWD (Lexogen) and sequenced, in two runs, with the use of an Illumina NextSeq500 platform, which generated at least 30 million reads/sample (75 bp Single End).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17232243" alias="GSM6510114_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17232243</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6510114_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6510114: T28_Sal5; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP394178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874089</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14798559">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14798559</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6510114</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6510114</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Fresh right lungs were immediately collected in RNAlater™ (Sigma, USA) for the next homogenization in QIAzol® Lysis Reagent (QIAGEN, Netherlands) with gentleMACS™ Dissociator (Miltenyi Biotec, Germany). RNA was extracted using the QIAcube robotic workstation with the miRNeasy Mini Kit (QIAGEN, Netherlands), including DNase digestion protocol. Libraries for massive parallel RNA sequencing (RNA-seq) were prepared with the QuantSeq 3' mRNA-Seq Library Prep Kit FWD (Lexogen) and sequenced, in two runs, with the use of an Illumina NextSeq500 platform, which generated at least 30 million reads/sample (75 bp Single End).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17232244" alias="GSM6510115_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17232244</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6510115_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6510115: T56_Blm6; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP394178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874089</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14798560">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14798560</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6510115</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6510115</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Fresh right lungs were immediately collected in RNAlater™ (Sigma, USA) for the next homogenization in QIAzol® Lysis Reagent (QIAGEN, Netherlands) with gentleMACS™ Dissociator (Miltenyi Biotec, Germany). RNA was extracted using the QIAcube robotic workstation with the miRNeasy Mini Kit (QIAGEN, Netherlands), including DNase digestion protocol. Libraries for massive parallel RNA sequencing (RNA-seq) were prepared with the QuantSeq 3' mRNA-Seq Library Prep Kit FWD (Lexogen) and sequenced, in two runs, with the use of an Illumina NextSeq500 platform, which generated at least 30 million reads/sample (75 bp Single End).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17232245" alias="GSM6510116_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17232245</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6510116_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6510116: T56_Blm7; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP394178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874089</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14798561">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14798561</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6510116</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6510116</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Fresh right lungs were immediately collected in RNAlater™ (Sigma, USA) for the next homogenization in QIAzol® Lysis Reagent (QIAGEN, Netherlands) with gentleMACS™ Dissociator (Miltenyi Biotec, Germany). RNA was extracted using the QIAcube robotic workstation with the miRNeasy Mini Kit (QIAGEN, Netherlands), including DNase digestion protocol. Libraries for massive parallel RNA sequencing (RNA-seq) were prepared with the QuantSeq 3' mRNA-Seq Library Prep Kit FWD (Lexogen) and sequenced, in two runs, with the use of an Illumina NextSeq500 platform, which generated at least 30 million reads/sample (75 bp Single End).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17232246" alias="GSM6510117_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17232246</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6510117_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6510117: T56_Sal6; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP394178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874089</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14798562">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14798562</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6510117</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6510117</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Fresh right lungs were immediately collected in RNAlater™ (Sigma, USA) for the next homogenization in QIAzol® Lysis Reagent (QIAGEN, Netherlands) with gentleMACS™ Dissociator (Miltenyi Biotec, Germany). RNA was extracted using the QIAcube robotic workstation with the miRNeasy Mini Kit (QIAGEN, Netherlands), including DNase digestion protocol. Libraries for massive parallel RNA sequencing (RNA-seq) were prepared with the QuantSeq 3' mRNA-Seq Library Prep Kit FWD (Lexogen) and sequenced, in two runs, with the use of an Illumina NextSeq500 platform, which generated at least 30 million reads/sample (75 bp Single End).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17232247" alias="GSM6510118_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17232247</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6510118_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6510118: T56_Sal7; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP394178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874089</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14798563">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14798563</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6510118</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6510118</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Fresh right lungs were immediately collected in RNAlater™ (Sigma, USA) for the next homogenization in QIAzol® Lysis Reagent (QIAGEN, Netherlands) with gentleMACS™ Dissociator (Miltenyi Biotec, Germany). RNA was extracted using the QIAcube robotic workstation with the miRNeasy Mini Kit (QIAGEN, Netherlands), including DNase digestion protocol. Libraries for massive parallel RNA sequencing (RNA-seq) were prepared with the QuantSeq 3' mRNA-Seq Library Prep Kit FWD (Lexogen) and sequenced, in two runs, with the use of an Illumina NextSeq500 platform, which generated at least 30 million reads/sample (75 bp Single End).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17232248" alias="GSM6510119_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17232248</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6510119_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6510119: T0_Naïve3-2; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP394178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874089</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14798564">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14798564</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6510119</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6510119</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Fresh right lungs were immediately collected in RNAlater™ (Sigma, USA) for the next homogenization in QIAzol® Lysis Reagent (QIAGEN, Netherlands) with gentleMACS™ Dissociator (Miltenyi Biotec, Germany). RNA was extracted using the QIAcube robotic workstation with the miRNeasy Mini Kit (QIAGEN, Netherlands), including DNase digestion protocol. Libraries for massive parallel RNA sequencing (RNA-seq) were prepared with the QuantSeq 3' mRNA-Seq Library Prep Kit FWD (Lexogen) and sequenced, in two runs, with the use of an Illumina NextSeq500 platform, which generated at least 30 million reads/sample (75 bp Single End).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17232249" alias="GSM6510120_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17232249</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6510120_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6510120: T14_Sal5; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP394178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874089</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14798565">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14798565</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6510120</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6510120</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Fresh right lungs were immediately collected in RNAlater™ (Sigma, USA) for the next homogenization in QIAzol® Lysis Reagent (QIAGEN, Netherlands) with gentleMACS™ Dissociator (Miltenyi Biotec, Germany). RNA was extracted using the QIAcube robotic workstation with the miRNeasy Mini Kit (QIAGEN, Netherlands), including DNase digestion protocol. Libraries for massive parallel RNA sequencing (RNA-seq) were prepared with the QuantSeq 3' mRNA-Seq Library Prep Kit FWD (Lexogen) and sequenced, in two runs, with the use of an Illumina NextSeq500 platform, which generated at least 30 million reads/sample (75 bp Single End).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17232250" alias="GSM6510121_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17232250</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6510121_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6510121: T14_Blm7; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP394178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874089</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14798566">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14798566</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6510121</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6510121</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Fresh right lungs were immediately collected in RNAlater™ (Sigma, USA) for the next homogenization in QIAzol® Lysis Reagent (QIAGEN, Netherlands) with gentleMACS™ Dissociator (Miltenyi Biotec, Germany). RNA was extracted using the QIAcube robotic workstation with the miRNeasy Mini Kit (QIAGEN, Netherlands), including DNase digestion protocol. Libraries for massive parallel RNA sequencing (RNA-seq) were prepared with the QuantSeq 3' mRNA-Seq Library Prep Kit FWD (Lexogen) and sequenced, in two runs, with the use of an Illumina NextSeq500 platform, which generated at least 30 million reads/sample (75 bp Single End).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17232251" alias="GSM6510122_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17232251</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6510122_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6510122: T21_Sal6; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP394178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874089</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14798567">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14798567</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6510122</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6510122</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Fresh right lungs were immediately collected in RNAlater™ (Sigma, USA) for the next homogenization in QIAzol® Lysis Reagent (QIAGEN, Netherlands) with gentleMACS™ Dissociator (Miltenyi Biotec, Germany). RNA was extracted using the QIAcube robotic workstation with the miRNeasy Mini Kit (QIAGEN, Netherlands), including DNase digestion protocol. Libraries for massive parallel RNA sequencing (RNA-seq) were prepared with the QuantSeq 3' mRNA-Seq Library Prep Kit FWD (Lexogen) and sequenced, in two runs, with the use of an Illumina NextSeq500 platform, which generated at least 30 million reads/sample (75 bp Single End).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17232252" alias="GSM6510123_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17232252</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6510123_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6510123: T21_Blm5; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP394178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874089</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14798568">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14798568</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6510123</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6510123</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Fresh right lungs were immediately collected in RNAlater™ (Sigma, USA) for the next homogenization in QIAzol® Lysis Reagent (QIAGEN, Netherlands) with gentleMACS™ Dissociator (Miltenyi Biotec, Germany). RNA was extracted using the QIAcube robotic workstation with the miRNeasy Mini Kit (QIAGEN, Netherlands), including DNase digestion protocol. Libraries for massive parallel RNA sequencing (RNA-seq) were prepared with the QuantSeq 3' mRNA-Seq Library Prep Kit FWD (Lexogen) and sequenced, in two runs, with the use of an Illumina NextSeq500 platform, which generated at least 30 million reads/sample (75 bp Single End).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17232253" alias="GSM6510124_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17232253</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6510124_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6510124: T21_Blm6; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP394178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874089</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14798569">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14798569</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6510124</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6510124</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Fresh right lungs were immediately collected in RNAlater™ (Sigma, USA) for the next homogenization in QIAzol® Lysis Reagent (QIAGEN, Netherlands) with gentleMACS™ Dissociator (Miltenyi Biotec, Germany). RNA was extracted using the QIAcube robotic workstation with the miRNeasy Mini Kit (QIAGEN, Netherlands), including DNase digestion protocol. Libraries for massive parallel RNA sequencing (RNA-seq) were prepared with the QuantSeq 3' mRNA-Seq Library Prep Kit FWD (Lexogen) and sequenced, in two runs, with the use of an Illumina NextSeq500 platform, which generated at least 30 million reads/sample (75 bp Single End).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17232254" alias="GSM6510125_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17232254</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6510125_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6510125: T28_Sal6; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP394178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874089</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14798570">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14798570</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6510125</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6510125</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Fresh right lungs were immediately collected in RNAlater™ (Sigma, USA) for the next homogenization in QIAzol® Lysis Reagent (QIAGEN, Netherlands) with gentleMACS™ Dissociator (Miltenyi Biotec, Germany). RNA was extracted using the QIAcube robotic workstation with the miRNeasy Mini Kit (QIAGEN, Netherlands), including DNase digestion protocol. Libraries for massive parallel RNA sequencing (RNA-seq) were prepared with the QuantSeq 3' mRNA-Seq Library Prep Kit FWD (Lexogen) and sequenced, in two runs, with the use of an Illumina NextSeq500 platform, which generated at least 30 million reads/sample (75 bp Single End).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17232255" alias="GSM6510126_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17232255</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6510126_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6510126: T28_Sal7; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP394178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874089</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14798571">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14798571</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6510126</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6510126</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Fresh right lungs were immediately collected in RNAlater™ (Sigma, USA) for the next homogenization in QIAzol® Lysis Reagent (QIAGEN, Netherlands) with gentleMACS™ Dissociator (Miltenyi Biotec, Germany). RNA was extracted using the QIAcube robotic workstation with the miRNeasy Mini Kit (QIAGEN, Netherlands), including DNase digestion protocol. Libraries for massive parallel RNA sequencing (RNA-seq) were prepared with the QuantSeq 3' mRNA-Seq Library Prep Kit FWD (Lexogen) and sequenced, in two runs, with the use of an Illumina NextSeq500 platform, which generated at least 30 million reads/sample (75 bp Single End).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17232256" alias="GSM6510127_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17232256</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6510127_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6510127: T28_Blm6; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP394178">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP394178</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA874089</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14798572">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14798572</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6510127</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6510127</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Fresh right lungs were immediately collected in RNAlater™ (Sigma, USA) for the next homogenization in QIAzol® Lysis Reagent (QIAGEN, Netherlands) with gentleMACS™ Dissociator (Miltenyi Biotec, Germany). RNA was extracted using the QIAcube robotic workstation with the miRNeasy Mini Kit (QIAGEN, Netherlands), including DNase digestion protocol. Libraries for massive parallel RNA sequencing (RNA-seq) were prepared with the QuantSeq 3' mRNA-Seq Library Prep Kit FWD (Lexogen) and sequenced, in two runs, with the use of an Illumina NextSeq500 platform, which generated at least 30 million reads/sample (75 bp Single End).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
