<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX12834730" alias="GSM5661481_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12834730</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5661481_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5661481: 3dps_62_S1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP343736">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP343736</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA776167</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10779561">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10779561</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5661481</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5661481</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>Culture plates were placed on ice for the extraction procedure. Cells were washed with 1ml of cold 1xPBS, suspended in 350µl of RLT-plus lysis buffer (Qiagen) and the total RNA was exctracted using RNEasy Plus Mini Kit (Qiagen). NEBNext Ultra II Directional RNA library after polyA purification</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12834731" alias="GSM5661482_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12834731</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5661482_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5661482: 3dps_63_S2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP343736">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP343736</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA776167</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10779562">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10779562</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5661482</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5661482</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>Culture plates were placed on ice for the extraction procedure. Cells were washed with 1ml of cold 1xPBS, suspended in 350µl of RLT-plus lysis buffer (Qiagen) and the total RNA was exctracted using RNEasy Plus Mini Kit (Qiagen). NEBNext Ultra II Directional RNA library after polyA purification</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12834732" alias="GSM5661483_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12834732</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5661483_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5661483: 3dps_67_S3; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP343736">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP343736</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA776167</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10779565">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10779565</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5661483</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5661483</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>Culture plates were placed on ice for the extraction procedure. Cells were washed with 1ml of cold 1xPBS, suspended in 350µl of RLT-plus lysis buffer (Qiagen) and the total RNA was exctracted using RNEasy Plus Mini Kit (Qiagen). NEBNext Ultra II Directional RNA library after polyA purification</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12834733" alias="GSM5661484_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12834733</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5661484_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5661484: 3dps_68_S4; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP343736">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP343736</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA776167</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10779567">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10779567</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5661484</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5661484</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>Culture plates were placed on ice for the extraction procedure. Cells were washed with 1ml of cold 1xPBS, suspended in 350µl of RLT-plus lysis buffer (Qiagen) and the total RNA was exctracted using RNEasy Plus Mini Kit (Qiagen). NEBNext Ultra II Directional RNA library after polyA purification</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12834734" alias="GSM5661485_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12834734</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5661485_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5661485: 3dps_70_S5; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP343736">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP343736</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA776167</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10779563">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10779563</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5661485</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5661485</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>Culture plates were placed on ice for the extraction procedure. Cells were washed with 1ml of cold 1xPBS, suspended in 350µl of RLT-plus lysis buffer (Qiagen) and the total RNA was exctracted using RNEasy Plus Mini Kit (Qiagen). NEBNext Ultra II Directional RNA library after polyA purification</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12834735" alias="GSM5661486_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12834735</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5661486_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5661486: 3dps_71_S6; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP343736">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP343736</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA776167</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10779564">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10779564</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5661486</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5661486</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>Culture plates were placed on ice for the extraction procedure. Cells were washed with 1ml of cold 1xPBS, suspended in 350µl of RLT-plus lysis buffer (Qiagen) and the total RNA was exctracted using RNEasy Plus Mini Kit (Qiagen). NEBNext Ultra II Directional RNA library after polyA purification</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12834736" alias="GSM5661487_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12834736</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5661487_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5661487: 3dps_72_S7; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP343736">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP343736</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA776167</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10779566">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10779566</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5661487</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5661487</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>Culture plates were placed on ice for the extraction procedure. Cells were washed with 1ml of cold 1xPBS, suspended in 350µl of RLT-plus lysis buffer (Qiagen) and the total RNA was exctracted using RNEasy Plus Mini Kit (Qiagen). NEBNext Ultra II Directional RNA library after polyA purification</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12834737" alias="GSM5661488_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12834737</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5661488_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5661488: 3dps_73_S8; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP343736">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP343736</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA776167</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10779568">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10779568</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5661488</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5661488</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>Culture plates were placed on ice for the extraction procedure. Cells were washed with 1ml of cold 1xPBS, suspended in 350µl of RLT-plus lysis buffer (Qiagen) and the total RNA was exctracted using RNEasy Plus Mini Kit (Qiagen). NEBNext Ultra II Directional RNA library after polyA purification</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12834738" alias="GSM5661489_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12834738</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5661489_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5661489: 3dps_74_S9; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP343736">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP343736</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA776167</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10779569">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10779569</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5661489</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5661489</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>Culture plates were placed on ice for the extraction procedure. Cells were washed with 1ml of cold 1xPBS, suspended in 350µl of RLT-plus lysis buffer (Qiagen) and the total RNA was exctracted using RNEasy Plus Mini Kit (Qiagen). NEBNext Ultra II Directional RNA library after polyA purification</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12834739" alias="GSM5661490_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12834739</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5661490_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5661490: 3dps_75_S10; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP343736">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP343736</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA776167</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10779570">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10779570</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5661490</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5661490</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>Culture plates were placed on ice for the extraction procedure. Cells were washed with 1ml of cold 1xPBS, suspended in 350µl of RLT-plus lysis buffer (Qiagen) and the total RNA was exctracted using RNEasy Plus Mini Kit (Qiagen). NEBNext Ultra II Directional RNA library after polyA purification</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12834740" alias="GSM5661491_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12834740</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5661491_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5661491: 3dps_Tgfb1_62_S11; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP343736">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP343736</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA776167</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10779571">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10779571</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5661491</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5661491</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>Culture plates were placed on ice for the extraction procedure. Cells were washed with 1ml of cold 1xPBS, suspended in 350µl of RLT-plus lysis buffer (Qiagen) and the total RNA was exctracted using RNEasy Plus Mini Kit (Qiagen). NEBNext Ultra II Directional RNA library after polyA purification</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12834741" alias="GSM5661492_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12834741</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5661492_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5661492: 3dps_Tgfb1_63_S12; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP343736">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP343736</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA776167</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10779572">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10779572</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5661492</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5661492</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>Culture plates were placed on ice for the extraction procedure. Cells were washed with 1ml of cold 1xPBS, suspended in 350µl of RLT-plus lysis buffer (Qiagen) and the total RNA was exctracted using RNEasy Plus Mini Kit (Qiagen). NEBNext Ultra II Directional RNA library after polyA purification</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12834742" alias="GSM5661493_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12834742</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5661493_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5661493: 3dps_Tgfb1_67_S13; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP343736">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP343736</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA776167</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10779573">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10779573</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5661493</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5661493</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>Culture plates were placed on ice for the extraction procedure. Cells were washed with 1ml of cold 1xPBS, suspended in 350µl of RLT-plus lysis buffer (Qiagen) and the total RNA was exctracted using RNEasy Plus Mini Kit (Qiagen). NEBNext Ultra II Directional RNA library after polyA purification</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12834743" alias="GSM5661494_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12834743</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5661494_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5661494: 3dps_Tgfb1_68_S14; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP343736">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP343736</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA776167</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10779574">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10779574</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5661494</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5661494</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>Culture plates were placed on ice for the extraction procedure. Cells were washed with 1ml of cold 1xPBS, suspended in 350µl of RLT-plus lysis buffer (Qiagen) and the total RNA was exctracted using RNEasy Plus Mini Kit (Qiagen). NEBNext Ultra II Directional RNA library after polyA purification</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12834744" alias="GSM5661495_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12834744</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5661495_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5661495: 3dps_Tgfb1_70_S15; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP343736">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP343736</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA776167</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10779575">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10779575</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5661495</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5661495</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>Culture plates were placed on ice for the extraction procedure. Cells were washed with 1ml of cold 1xPBS, suspended in 350µl of RLT-plus lysis buffer (Qiagen) and the total RNA was exctracted using RNEasy Plus Mini Kit (Qiagen). NEBNext Ultra II Directional RNA library after polyA purification</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12834745" alias="GSM5661496_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12834745</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5661496_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5661496: 3dps_Tgfb1_71_S16; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP343736">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP343736</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA776167</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10779576">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10779576</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5661496</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5661496</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>Culture plates were placed on ice for the extraction procedure. Cells were washed with 1ml of cold 1xPBS, suspended in 350µl of RLT-plus lysis buffer (Qiagen) and the total RNA was exctracted using RNEasy Plus Mini Kit (Qiagen). NEBNext Ultra II Directional RNA library after polyA purification</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12834746" alias="GSM5661497_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12834746</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5661497_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5661497: 3dps_Tgfb1_72_S17; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP343736">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP343736</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA776167</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10779577">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10779577</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5661497</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5661497</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>Culture plates were placed on ice for the extraction procedure. Cells were washed with 1ml of cold 1xPBS, suspended in 350µl of RLT-plus lysis buffer (Qiagen) and the total RNA was exctracted using RNEasy Plus Mini Kit (Qiagen). NEBNext Ultra II Directional RNA library after polyA purification</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12834747" alias="GSM5661498_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12834747</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5661498_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5661498: 3dps_Tgfb1_73_S18; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP343736">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP343736</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA776167</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10779578">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10779578</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5661498</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5661498</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>Culture plates were placed on ice for the extraction procedure. Cells were washed with 1ml of cold 1xPBS, suspended in 350µl of RLT-plus lysis buffer (Qiagen) and the total RNA was exctracted using RNEasy Plus Mini Kit (Qiagen). NEBNext Ultra II Directional RNA library after polyA purification</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12834748" alias="GSM5661499_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12834748</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5661499_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5661499: 3dps_Tgfb1_74_S19; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP343736">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP343736</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA776167</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10779579">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10779579</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5661499</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5661499</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>Culture plates were placed on ice for the extraction procedure. Cells were washed with 1ml of cold 1xPBS, suspended in 350µl of RLT-plus lysis buffer (Qiagen) and the total RNA was exctracted using RNEasy Plus Mini Kit (Qiagen). NEBNext Ultra II Directional RNA library after polyA purification</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12834749" alias="GSM5661500_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12834749</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5661500_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5661500: 3dps_Tgfb1_75_S20; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP343736">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP343736</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA776167</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10779580">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10779580</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5661500</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5661500</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>Culture plates were placed on ice for the extraction procedure. Cells were washed with 1ml of cold 1xPBS, suspended in 350µl of RLT-plus lysis buffer (Qiagen) and the total RNA was exctracted using RNEasy Plus Mini Kit (Qiagen). NEBNext Ultra II Directional RNA library after polyA purification</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12834750" alias="GSM5661501_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12834750</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5661501_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5661501: 3dps_IL12_62_S21; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP343736">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP343736</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA776167</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10779581">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10779581</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5661501</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5661501</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>Culture plates were placed on ice for the extraction procedure. Cells were washed with 1ml of cold 1xPBS, suspended in 350µl of RLT-plus lysis buffer (Qiagen) and the total RNA was exctracted using RNEasy Plus Mini Kit (Qiagen). NEBNext Ultra II Directional RNA library after polyA purification</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12834751" alias="GSM5661502_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12834751</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5661502_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5661502: 3dps_IL12_63_S22; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP343736">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP343736</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA776167</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10779582">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10779582</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5661502</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5661502</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>Culture plates were placed on ice for the extraction procedure. Cells were washed with 1ml of cold 1xPBS, suspended in 350µl of RLT-plus lysis buffer (Qiagen) and the total RNA was exctracted using RNEasy Plus Mini Kit (Qiagen). NEBNext Ultra II Directional RNA library after polyA purification</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12834752" alias="GSM5661503_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12834752</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5661503_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5661503: 3dps_IL12_67_S23; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP343736">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP343736</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA776167</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10779583">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10779583</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5661503</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5661503</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>Culture plates were placed on ice for the extraction procedure. Cells were washed with 1ml of cold 1xPBS, suspended in 350µl of RLT-plus lysis buffer (Qiagen) and the total RNA was exctracted using RNEasy Plus Mini Kit (Qiagen). NEBNext Ultra II Directional RNA library after polyA purification</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12834753" alias="GSM5661504_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12834753</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5661504_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5661504: 3dps_IL12_68_S24; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP343736">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP343736</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA776167</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10779584">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10779584</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5661504</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5661504</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>Culture plates were placed on ice for the extraction procedure. Cells were washed with 1ml of cold 1xPBS, suspended in 350µl of RLT-plus lysis buffer (Qiagen) and the total RNA was exctracted using RNEasy Plus Mini Kit (Qiagen). NEBNext Ultra II Directional RNA library after polyA purification</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12834754" alias="GSM5661505_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12834754</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5661505_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5661505: 3dps_IL12_70_S25; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP343736">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP343736</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA776167</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10779585">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10779585</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5661505</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5661505</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>Culture plates were placed on ice for the extraction procedure. Cells were washed with 1ml of cold 1xPBS, suspended in 350µl of RLT-plus lysis buffer (Qiagen) and the total RNA was exctracted using RNEasy Plus Mini Kit (Qiagen). NEBNext Ultra II Directional RNA library after polyA purification</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12834755" alias="GSM5661506_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12834755</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5661506_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5661506: 3dps_IL12_71_S26; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP343736">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP343736</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA776167</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10779586">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10779586</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5661506</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5661506</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>Culture plates were placed on ice for the extraction procedure. Cells were washed with 1ml of cold 1xPBS, suspended in 350µl of RLT-plus lysis buffer (Qiagen) and the total RNA was exctracted using RNEasy Plus Mini Kit (Qiagen). NEBNext Ultra II Directional RNA library after polyA purification</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12834756" alias="GSM5661507_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12834756</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5661507_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5661507: 3dps_IL12_72_S27; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP343736">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP343736</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA776167</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10779587">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10779587</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5661507</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5661507</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>Culture plates were placed on ice for the extraction procedure. Cells were washed with 1ml of cold 1xPBS, suspended in 350µl of RLT-plus lysis buffer (Qiagen) and the total RNA was exctracted using RNEasy Plus Mini Kit (Qiagen). NEBNext Ultra II Directional RNA library after polyA purification</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12834757" alias="GSM5661508_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12834757</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5661508_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5661508: 3dps_IL12_73_S28; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP343736">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP343736</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA776167</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10779588">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10779588</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5661508</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5661508</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>Culture plates were placed on ice for the extraction procedure. Cells were washed with 1ml of cold 1xPBS, suspended in 350µl of RLT-plus lysis buffer (Qiagen) and the total RNA was exctracted using RNEasy Plus Mini Kit (Qiagen). NEBNext Ultra II Directional RNA library after polyA purification</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12834758" alias="GSM5661509_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12834758</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5661509_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5661509: 3dps_IL12_74_S29; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP343736">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP343736</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA776167</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10779589">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10779589</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5661509</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5661509</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>Culture plates were placed on ice for the extraction procedure. Cells were washed with 1ml of cold 1xPBS, suspended in 350µl of RLT-plus lysis buffer (Qiagen) and the total RNA was exctracted using RNEasy Plus Mini Kit (Qiagen). NEBNext Ultra II Directional RNA library after polyA purification</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12834759" alias="GSM5661510_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12834759</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5661510_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5661510: 3dps_IL12_75_S30; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP343736">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP343736</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA776167</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10779590">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10779590</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5661510</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5661510</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>Culture plates were placed on ice for the extraction procedure. Cells were washed with 1ml of cold 1xPBS, suspended in 350µl of RLT-plus lysis buffer (Qiagen) and the total RNA was exctracted using RNEasy Plus Mini Kit (Qiagen). NEBNext Ultra II Directional RNA library after polyA purification</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
