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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX14313189" alias="GSM5922114_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313189</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922114_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922114: C119_B6_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129336">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129336</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922114</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922114</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313190" alias="GSM5922115_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313190</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922115_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922115: C119_B7_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129335">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129335</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922115</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922115</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313191" alias="GSM5922116_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313191</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922116_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922116: C119_B8_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129337">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129337</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922116</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922116</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313192" alias="GSM5922117_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313192</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922117_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922117: C119_B9_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129338">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129338</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922117</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922117</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313193" alias="GSM5922118_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313193</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922118_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922118: C119_C1_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129340">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129340</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922118</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922118</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313194" alias="GSM5922119_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313194</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922119_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922119: C119_C10_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129339">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129339</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922119</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922119</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313195" alias="GSM5922120_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313195</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922120_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922120: C119_C11_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129342">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129342</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922120</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922120</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313196" alias="GSM5922121_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313196</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922121_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922121: C119_C12_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129341">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129341</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922121</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922121</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313197" alias="GSM5922122_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313197</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922122_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922122: C119_C3_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129344">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129344</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922122</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922122</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313198" alias="GSM5922123_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313198</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922123_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922123: C119_C6_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129343">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129343</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922123</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922123</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313199" alias="GSM5922172_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313199</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922172_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922172: C119_H9_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129345">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129345</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922172</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922172</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313200" alias="GSM5922173_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313200</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922173_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922173: C128_A10_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129346">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129346</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922173</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922173</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313201" alias="GSM5922174_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313201</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922174_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922174: C128_A11_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129347">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129347</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922174</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922174</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313202" alias="GSM5922175_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313202</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922175_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922175: C128_A3_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129348">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129348</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922175</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922175</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313203" alias="GSM5922176_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313203</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922176_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922176: C128_A6_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129349">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129349</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922176</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922176</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313204" alias="GSM5922177_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313204</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922177_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922177: C128_A7_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129350">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129350</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922177</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922177</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313205" alias="GSM5922178_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313205</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922178_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922178: C128_A8_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129351">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129351</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922178</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922178</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313206" alias="GSM5922179_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313206</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922179_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922179: C128_A9_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129352">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129352</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922179</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922179</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313207" alias="GSM5922180_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313207</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922180_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922180: C128_B1_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129353">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129353</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922180</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922180</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313208" alias="GSM5922181_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313208</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922181_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922181: C128_B10_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129354">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129354</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922181</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922181</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313209" alias="GSM5922182_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313209</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922182_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922182: C128_B11_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129355">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129355</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922182</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922182</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313210" alias="GSM5922183_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313210</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922183_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922183: C128_B12_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129356">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129356</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922183</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922183</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313211" alias="GSM5922184_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313211</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922184_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922184: C128_B2_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129357">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129357</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922184</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922184</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313212" alias="GSM5922185_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313212</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922185_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922185: C128_B3_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129358">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129358</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922185</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922185</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313213" alias="GSM5922186_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313213</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922186_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922186: C128_B4_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129360">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129360</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922186</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922186</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313214" alias="GSM5922187_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313214</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922187_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922187: C128_B5_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129359">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129359</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922187</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922187</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313215" alias="GSM5922284_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313215</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922284_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922284: C129_C7_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129361">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129361</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922284</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922284</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313216" alias="GSM5922285_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313216</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922285_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922285: C129_C8_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129362">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129362</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922285</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922285</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313217" alias="GSM5922286_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313217</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922286_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922286: C129_D1_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129363">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129363</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922286</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922286</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313218" alias="GSM5922287_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313218</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922287_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922287: C129_D10_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129364">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129364</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922287</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922287</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313219" alias="GSM5922288_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313219</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922288_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922288: C129_D11_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129366">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129366</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922288</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922288</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313220" alias="GSM5922289_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313220</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922289_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922289: C129_D12_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129365">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129365</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922289</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922289</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313221" alias="GSM5922290_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313221</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922290_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922290: C129_D2_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129368">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129368</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922290</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922290</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313222" alias="GSM5922291_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313222</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922291_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922291: C129_D5_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129367">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129367</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922291</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922291</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313223" alias="GSM5922292_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313223</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922292_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922292: C129_D6_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129369">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129369</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922292</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922292</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313224" alias="GSM5922293_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313224</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922293_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922293: C129_D7_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129370">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129370</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922293</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922293</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313225" alias="GSM5922294_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313225</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922294_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922294: C129_D8_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129372">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129372</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922294</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922294</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313226" alias="GSM5922295_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313226</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922295_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922295: C129_E1_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129371">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129371</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922295</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922295</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313227" alias="GSM5922296_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313227</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922296_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922296: C129_E10_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129373">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129373</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922296</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922296</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313228" alias="GSM5922297_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313228</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922297_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922297: C129_E11_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129375">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129375</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922297</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922297</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313229" alias="GSM5922298_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313229</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922298_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922298: C129_E12_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129374">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129374</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922298</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922298</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313230" alias="GSM5922299_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313230</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922299_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922299: C129_E2_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129376">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129376</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922299</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922299</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313231" alias="GSM5922060_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313231</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922060_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922060: C114_F1_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129377">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129377</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922060</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922060</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313232" alias="GSM5922061_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313232</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922061_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922061: C114_F1_L1_38w_RepI_IDTILL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129378">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129378</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922061</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922061</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313233" alias="GSM5922062_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313233</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922062_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922062: C114_F2_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129380">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129380</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922062</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922062</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313234" alias="GSM5922063_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313234</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922063_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922063: C114_F2_L1_38w_RepI_IDTILL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129379">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129379</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922063</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922063</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313235" alias="GSM5922064_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313235</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922064_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922064: C114_F3_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129381">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129381</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922064</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922064</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313236" alias="GSM5922065_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313236</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922065_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922065: C114_F3_L1_38w_RepI_IDTILL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129383">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129383</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922065</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922065</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313237" alias="GSM5922066_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313237</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922066_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922066: C114_F4_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129382">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129382</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922066</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922066</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313238" alias="GSM5922067_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313238</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922067_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922067: C114_F4_L1_38w_RepI_IDTILL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129384">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129384</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922067</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922067</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313239" alias="GSM5922068_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313239</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922068_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922068: C114_F5_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129386">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129386</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922068</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922068</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313240" alias="GSM5922069_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313240</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922069_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922069: C114_F6_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129385">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129385</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922069</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922069</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313241" alias="GSM5922070_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313241</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922070_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922070: C114_G1_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129387">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129387</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922070</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922070</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313242" alias="GSM5922071_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313242</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922071_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922071: C114_G2_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129389">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129389</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922071</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922071</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313243" alias="GSM5922072_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313243</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922072_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922072: C114_G2_L1_38w_RepI_IDTILL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129388">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129388</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922072</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922072</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313244" alias="GSM5922073_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313244</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922073_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922073: C114_G3_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129390">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129390</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922073</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922073</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313245" alias="GSM5922074_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313245</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922074_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922074: C114_G3_L1_38w_RepI__IDTILL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129392">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129392</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922074</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922074</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313246" alias="GSM5922075_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313246</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922075_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922075: C114_G4_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129391">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129391</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922075</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922075</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313247" alias="GSM5922076_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313247</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922076_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922076: C114_G5_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129393">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129393</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922076</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922076</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313248" alias="GSM5922077_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313248</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922077_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922077: C114_G5_L1_38w_RepI__IDTILL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129395">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129395</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922077</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922077</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313249" alias="GSM5922078_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313249</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922078_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922078: C114_G6_L1_38w_RepI__IDTILL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129394">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129394</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922078</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922078</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313250" alias="GSM5922079_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313250</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922079_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922079: C114_H1_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129396">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129396</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922079</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922079</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313251" alias="GSM5922080_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313251</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922080_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922080: C114_H3_L1_38w_RepI_IDTILL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129397">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129397</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922080</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922080</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313252" alias="GSM5922081_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313252</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922081_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922081: C118_A10_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129398">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129398</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922081</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922081</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313253" alias="GSM5922082_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313253</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922082_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922082: C118_A11_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129399">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129399</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922082</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922082</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313254" alias="GSM5922083_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313254</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922083_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922083: C118_A12_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129400">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129400</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922083</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922083</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313255" alias="GSM5922084_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313255</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922084_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922084: C118_A3_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129401">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129401</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922084</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922084</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313256" alias="GSM5922085_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313256</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922085_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922085: C118_A4_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129402">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129402</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922085</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922085</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313257" alias="GSM5922086_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313257</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922086_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922086: C118_A5_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129403">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129403</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922086</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922086</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313258" alias="GSM5922087_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313258</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922087_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922087: C118_A6_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129404">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129404</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922087</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922087</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313259" alias="GSM5922088_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313259</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922088_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922088: C118_A7_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129405">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129405</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922088</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922088</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313260" alias="GSM5922089_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313260</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922089_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922089: C118_A8_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129406">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129406</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922089</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922089</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313261" alias="GSM5922090_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313261</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922090_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922090: C118_A9_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129407">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129407</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922090</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922090</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313262" alias="GSM5922091_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313262</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922091_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922091: C118_B10_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129408">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129408</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922091</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922091</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313263" alias="GSM5922124_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313263</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922124_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922124: C119_C7_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129409">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129409</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922124</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922124</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313264" alias="GSM5922125_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313264</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922125_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922125: C119_C9_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129410">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129410</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922125</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922125</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313265" alias="GSM5922126_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313265</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922126_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922126: C119_D1_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129411">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129411</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922126</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922126</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313266" alias="GSM5922127_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313266</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922127_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922127: C119_D10_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129412">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129412</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922127</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922127</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313267" alias="GSM5922128_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313267</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922128_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922128: C119_D11_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129413">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129413</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922128</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922128</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313268" alias="GSM5922129_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313268</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922129_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922129: C119_D12_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129414">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129414</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922129</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922129</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313269" alias="GSM5922130_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313269</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922130_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922130: C119_D2_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129415">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129415</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922130</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922130</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313270" alias="GSM5922131_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313270</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922131_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922131: C119_D3_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129416">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129416</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922131</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922131</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313271" alias="GSM5922132_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313271</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922132_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922132: C119_D4_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129417">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129417</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922132</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922132</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313272" alias="GSM5922133_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313272</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922133_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922133: C119_D7_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129418">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129418</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922133</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922133</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313273" alias="GSM5922134_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313273</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922134_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922134: C119_D8_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129420">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129420</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922134</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922134</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313274" alias="GSM5922135_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313274</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922135_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922135: C119_D9_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129419">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129419</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922135</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922135</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313275" alias="GSM5922136_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313275</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922136_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922136: C119_E1_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129421">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129421</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922136</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922136</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313276" alias="GSM5922137_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313276</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922137_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922137: C119_E11_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129424">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129424</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922137</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922137</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313277" alias="GSM5922138_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313277</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922138_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922138: C119_E12_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129422">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129422</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922138</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922138</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313278" alias="GSM5922139_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313278</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922139_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922139: C119_E2_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129423">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129423</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922139</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922139</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313279" alias="GSM5922188_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313279</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922188_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922188: C128_B6_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129425">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129425</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922188</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922188</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313280" alias="GSM5922189_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313280</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922189_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922189: C128_B7_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129426">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129426</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922189</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922189</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313281" alias="GSM5922190_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313281</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922190_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922190: C128_B8_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129427">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129427</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922190</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922190</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313282" alias="GSM5922191_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313282</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922191_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922191: C128_B9_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129428">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129428</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922191</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922191</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313283" alias="GSM5922192_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313283</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922192_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922192: C128_C1_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129429">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129429</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922192</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922192</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313284" alias="GSM5922193_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313284</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922193_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922193: C128_C10_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129430">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129430</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922193</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922193</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313285" alias="GSM5922194_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313285</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922194_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922194: C128_C11_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129431">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129431</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922194</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922194</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313286" alias="GSM5922195_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313286</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922195_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922195: C128_C12_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129432">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129432</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922195</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922195</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313287" alias="GSM5922196_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313287</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922196_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922196: C128_C3_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129433">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129433</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922196</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922196</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313288" alias="GSM5922197_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313288</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922197_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922197: C128_C4_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129434">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129434</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922197</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922197</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313289" alias="GSM5922198_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313289</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922198_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922198: C128_C5_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129435">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129435</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922198</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922198</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313290" alias="GSM5922199_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313290</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922199_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922199: C128_C6_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129436">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129436</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922199</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922199</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313291" alias="GSM5922200_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313291</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922200_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922200: C128_C7_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129437">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129437</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922200</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922200</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313292" alias="GSM5922201_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313292</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922201_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922201: C128_C8_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129438">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129438</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922201</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922201</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313293" alias="GSM5922202_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313293</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922202_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922202: C128_C9_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129439">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129439</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922202</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922202</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313294" alias="GSM5922203_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313294</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922203_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922203: C128_D1_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129440">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129440</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922203</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922203</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313295" alias="GSM5922236_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313295</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922236_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922236: C128_F9_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129441">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129441</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922236</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922236</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313296" alias="GSM5922237_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313296</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922237_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922237: C128_G1_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129442">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129442</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922237</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922237</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313297" alias="GSM5922238_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313297</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922238_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922238: C128_G10_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129443">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129443</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922238</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922238</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313298" alias="GSM5922239_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313298</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922239_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922239: C128_G11_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129444">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129444</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922239</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922239</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313299" alias="GSM5922240_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313299</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922240_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922240: C128_G12_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129445">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129445</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922240</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922240</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313300" alias="GSM5922241_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313300</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922241_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922241: C128_G2_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129447">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129447</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922241</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922241</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313301" alias="GSM5922242_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313301</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922242_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922242: C128_G3_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129446">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129446</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922242</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922242</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313302" alias="GSM5922243_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313302</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922243_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922243: C128_G4_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129448">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129448</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922243</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922243</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313303" alias="GSM5922244_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313303</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922244_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922244: C128_G5_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129450">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129450</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922244</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922244</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313304" alias="GSM5922245_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313304</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922245_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922245: C128_G6_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129449">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129449</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922245</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922245</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313305" alias="GSM5922246_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313305</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922246_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922246: C128_G7_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129451">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129451</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922246</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922246</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313306" alias="GSM5922247_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313306</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922247_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922247: C128_G8_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129453">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129453</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922247</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922247</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313307" alias="GSM5922248_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313307</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922248_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922248: C128_G9_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129452">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129452</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922248</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922248</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313308" alias="GSM5922249_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313308</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922249_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922249: C128_H1_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129454">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129454</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922249</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922249</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313309" alias="GSM5922250_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313309</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922250_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922250: C128_H10_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129455">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129455</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922250</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922250</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313310" alias="GSM5922251_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313310</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922251_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922251: C128_H2_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129457">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129457</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922251</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922251</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313311" alias="GSM5922300_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313311</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922300_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922300: C129_E3_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129456">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129456</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922300</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922300</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313312" alias="GSM5922301_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313312</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922301_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922301: C129_E4_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129458">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129458</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922301</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922301</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313313" alias="GSM5922302_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313313</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922302_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922302: C129_E5_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129459">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129459</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922302</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922302</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313314" alias="GSM5922303_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313314</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922303_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922303: C129_E6_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129460">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129460</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922303</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922303</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313315" alias="GSM5922304_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313315</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922304_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922304: C129_E7_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129462">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129462</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922304</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922304</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313316" alias="GSM5922305_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313316</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922305_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922305: C129_E8_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129461">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129461</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922305</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922305</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313317" alias="GSM5922306_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313317</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922306_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922306: C129_F1_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129463">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129463</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922306</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922306</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313318" alias="GSM5922307_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313318</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922307_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922307: C129_F11_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129466">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129466</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922307</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922307</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313319" alias="GSM5922308_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313319</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922308_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922308: C129_F12_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129464">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129464</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922308</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922308</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313320" alias="GSM5922309_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313320</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922309_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922309: C129_F2_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129465">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129465</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922309</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922309</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313321" alias="GSM5922310_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313321</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922310_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922310: C129_F3_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129468">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129468</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922310</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922310</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313322" alias="GSM5922311_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313322</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922311_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922311: C129_F4_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129467">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129467</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922311</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922311</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313323" alias="GSM5922312_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313323</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922312_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922312: C129_F5_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129469">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129469</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922312</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922312</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313324" alias="GSM5922313_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313324</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922313_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922313: C129_F6_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129470">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129470</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922313</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922313</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313325" alias="GSM5922314_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313325</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922314_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922314: C129_F7_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129472">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129472</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922314</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922314</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313326" alias="GSM5922315_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313326</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922315_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922315: C129_F8_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129471">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129471</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922315</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922315</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313327" alias="GSM5922028_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313327</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922028_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922028: C114_A10_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129475">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129475</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922028</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922028</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313328" alias="GSM5922029_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313328</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922029_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922029: C114_A2_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129474">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129474</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922029</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922029</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313329" alias="GSM5922030_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313329</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922030_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922030: C114_A7_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129473">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129473</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922030</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922030</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313330" alias="GSM5922031_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313330</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922031_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922031: C114_A8_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129477">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129477</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922031</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922031</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313331" alias="GSM5922032_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313331</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922032_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922032: C114_A9_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129476">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129476</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922032</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922032</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313332" alias="GSM5922033_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313332</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922033_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922033: C114_B10_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129478">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129478</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922033</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922033</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313333" alias="GSM5922034_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313333</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922034_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922034: C114_B12_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129479">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129479</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922034</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922034</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313334" alias="GSM5922035_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313334</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922035_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922035: C114_B7_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129480">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129480</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922035</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922035</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313335" alias="GSM5922036_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313335</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922036_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922036: C114_B8_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129481">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129481</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922036</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922036</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313336" alias="GSM5922037_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313336</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922037_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922037: C114_B9_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129484">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129484</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922037</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922037</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313337" alias="GSM5922038_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313337</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922038_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922038: C114_C10_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129482">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129482</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922038</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922038</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313338" alias="GSM5922039_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313338</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922039_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922039: C114_C12_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129483">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129483</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922039</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922039</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313339" alias="GSM5922040_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313339</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922040_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922040: C114_C3_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129485">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129485</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922040</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922040</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313340" alias="GSM5922041_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313340</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922041_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922041: C114_C7_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129486">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129486</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922041</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922041</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313341" alias="GSM5922042_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313341</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922042_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922042: C114_C8_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129487">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129487</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922042</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922042</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313342" alias="GSM5922043_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313342</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922043_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922043: C114_C9_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129489">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129489</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922043</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922043</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313343" alias="GSM5922332_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313343</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922332_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922332: C129_H3_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129488">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129488</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922332</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922332</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313344" alias="GSM5922333_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313344</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922333_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922333: C129_H4_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129490">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129490</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922333</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922333</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313345" alias="GSM5922334_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313345</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922334_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922334: C129_H5_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129491">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129491</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922334</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922334</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313346" alias="GSM5922335_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313346</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922335_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922335: C129_H6_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129492">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129492</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922335</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922335</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313347" alias="GSM5922336_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313347</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922336_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922336: C129_H7_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129495">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129495</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922336</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922336</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313348" alias="GSM5922337_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313348</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922337_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922337: C129_H8_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129493">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129493</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922337</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922337</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313349" alias="GSM5922140_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313349</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922140_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922140: C119_E3_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129494">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129494</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922140</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922140</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313350" alias="GSM5922141_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313350</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922141_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922141: C119_E4_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129496">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129496</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922141</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922141</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313351" alias="GSM5922142_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313351</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922142_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922142: C119_E7_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129498">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129498</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922142</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922142</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313352" alias="GSM5922143_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313352</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922143_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922143: C119_E9_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129497">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129497</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922143</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922143</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313353" alias="GSM5922144_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313353</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922144_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922144: C119_F1_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129499">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129499</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922144</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922144</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313354" alias="GSM5922145_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313354</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922145_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922145: C119_F10_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129500">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129500</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922145</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922145</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313355" alias="GSM5922146_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313355</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922146_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922146: C119_F11_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129501">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129501</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922146</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922146</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313356" alias="GSM5922147_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313356</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922147_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922147: C119_F12_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129502">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129502</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922147</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922147</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313357" alias="GSM5922148_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313357</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922148_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922148: C119_F2_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129503">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129503</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922148</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922148</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313358" alias="GSM5922149_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313358</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922149_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922149: C119_F3_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129504">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129504</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922149</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922149</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313359" alias="GSM5922150_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313359</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922150_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922150: C119_F4_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129505">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129505</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922150</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922150</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313360" alias="GSM5922151_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313360</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922151_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922151: C119_F8_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129506">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129506</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922151</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922151</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313361" alias="GSM5922152_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313361</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922152_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922152: C119_F9_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129508">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129508</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922152</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922152</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313362" alias="GSM5922153_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313362</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922153_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922153: C119_G1_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129507">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129507</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922153</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922153</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313363" alias="GSM5922154_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313363</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922154_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922154: C119_G10_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129509">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129509</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922154</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922154</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313364" alias="GSM5922155_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313364</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922155_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922155: C119_G11_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129510">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129510</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922155</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922155</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313365" alias="GSM5922204_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313365</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922204_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922204: C128_D10_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129511">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129511</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922204</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922204</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313366" alias="GSM5922205_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313366</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922205_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922205: C128_D11_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129512">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129512</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922205</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922205</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313367" alias="GSM5922206_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313367</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922206_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922206: C128_D12_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129513">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129513</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922206</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922206</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313368" alias="GSM5922207_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313368</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922207_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922207: C128_D2_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129514">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129514</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922207</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922207</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313369" alias="GSM5922208_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313369</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922208_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922208: C128_D4_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129515">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129515</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922208</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922208</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313370" alias="GSM5922209_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313370</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922209_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922209: C128_D5_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129516">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129516</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922209</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922209</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313371" alias="GSM5922210_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313371</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922210_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922210: C128_D6_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129517">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129517</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922210</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922210</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313372" alias="GSM5922211_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313372</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922211_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922211: C128_D7_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129518">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129518</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922211</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922211</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313373" alias="GSM5922212_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313373</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922212_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922212: C128_D8_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129520">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129520</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922212</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922212</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313374" alias="GSM5922213_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313374</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922213_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922213: C128_D9_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129519">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129519</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922213</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922213</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313375" alias="GSM5922214_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313375</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922214_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922214: C128_E10_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129521">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129521</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922214</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922214</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313376" alias="GSM5922215_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313376</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922215_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922215: C128_E11_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129523">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129523</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922215</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922215</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313377" alias="GSM5922216_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313377</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922216_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922216: C128_E12_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129522">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129522</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922216</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922216</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313378" alias="GSM5922217_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313378</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922217_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922217: C128_E2_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129524">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129524</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922217</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922217</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313379" alias="GSM5922218_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313379</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922218_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922218: C128_E3_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129526">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129526</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922218</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922218</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313380" alias="GSM5922219_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313380</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922219_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922219: C128_E4_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129525">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129525</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922219</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922219</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313381" alias="GSM5922220_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313381</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922220_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922220: C128_E5_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129527">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129527</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922220</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922220</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313382" alias="GSM5922221_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313382</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922221_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922221: C128_E6_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129528">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129528</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922221</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922221</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313383" alias="GSM5922222_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313383</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922222_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922222: C128_E7_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129529">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129529</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922222</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922222</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313384" alias="GSM5922223_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313384</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922223_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922223: C128_E8_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129530">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129530</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922223</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922223</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313385" alias="GSM5922224_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313385</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922224_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922224: C128_E9_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129531">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129531</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922224</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922224</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313386" alias="GSM5922225_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313386</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922225_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922225: C128_F1_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129532">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129532</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922225</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922225</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313387" alias="GSM5922226_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313387</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922226_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922226: C128_F10_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129533">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129533</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922226</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922226</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313388" alias="GSM5922227_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313388</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922227_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922227: C128_F11_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129534">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129534</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922227</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922227</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313389" alias="GSM5922228_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313389</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922228_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922228: C128_F12_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129535">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129535</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922228</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922228</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313390" alias="GSM5922229_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313390</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922229_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922229: C128_F2_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129536">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129536</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922229</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922229</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313391" alias="GSM5922230_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313391</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922230_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922230: C128_F3_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129538">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129538</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922230</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922230</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313392" alias="GSM5922231_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313392</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922231_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922231: C128_F4_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129537">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129537</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922231</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922231</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313393" alias="GSM5922232_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313393</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922232_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922232: C128_F5_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129539">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129539</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922232</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922232</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313394" alias="GSM5922233_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313394</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922233_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922233: C128_F6_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129541">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129541</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922233</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922233</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313395" alias="GSM5922234_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313395</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922234_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922234: C128_F7_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129540">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129540</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922234</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922234</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313396" alias="GSM5922235_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313396</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922235_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922235: C128_F8_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129542">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129542</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922235</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922235</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313397" alias="GSM5922252_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313397</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922252_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922252: C128_H4_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129544">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129544</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922252</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922252</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313398" alias="GSM5922253_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313398</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922253_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922253: C128_H6_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129543">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129543</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922253</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922253</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313399" alias="GSM5922254_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313399</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922254_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922254: C128_H9_L1_38wUW_RepM; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129545">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129545</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922254</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922254</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313400" alias="GSM5922255_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313400</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922255_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922255: C129_A10_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129546">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129546</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922255</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922255</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313401" alias="GSM5922256_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313401</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922256_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922256: C129_A11_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129547">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129547</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922256</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922256</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313402" alias="GSM5922257_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313402</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922257_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922257: C129_A12_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129548">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129548</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922257</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922257</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313403" alias="GSM5922258_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313403</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922258_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922258: C129_A2_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129549">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129549</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922258</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922258</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313404" alias="GSM5922259_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313404</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922259_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922259: C129_A3_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129550">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129550</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922259</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922259</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313405" alias="GSM5922260_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313405</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922260_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922260: C129_A4_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129551">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129551</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922260</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922260</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313406" alias="GSM5922261_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313406</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922261_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922261: C129_A5_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129552">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129552</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922261</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922261</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313407" alias="GSM5922262_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313407</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922262_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922262: C129_A6_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129553">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129553</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922262</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922262</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313408" alias="GSM5922263_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313408</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922263_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922263: C129_A7_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129554">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129554</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922263</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922263</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313409" alias="GSM5922264_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313409</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922264_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922264: C129_A8_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129555">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129555</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922264</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922264</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313410" alias="GSM5922265_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313410</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922265_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922265: C129_B1_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129556">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129556</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922265</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922265</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313411" alias="GSM5922266_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313411</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922266_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922266: C129_B11_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129557">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129557</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922266</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922266</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313412" alias="GSM5922267_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313412</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922267_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922267: C129_B12_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129558">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129558</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922267</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922267</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313413" alias="GSM5922316_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313413</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922316_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922316: C129_G1_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129559">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129559</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922316</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922316</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313414" alias="GSM5922317_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313414</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922317_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922317: C129_G10_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129560">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129560</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922317</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922317</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313415" alias="GSM5922318_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313415</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922318_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922318: C129_G11_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129561">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129561</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922318</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922318</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313416" alias="GSM5922319_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313416</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922319_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922319: C129_G12_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129563">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129563</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922319</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922319</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313417" alias="GSM5922320_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313417</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922320_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922320: C129_G2_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129562">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129562</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922320</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922320</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313418" alias="GSM5922321_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313418</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922321_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922321: C129_G3_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129564">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129564</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922321</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922321</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313419" alias="GSM5922322_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313419</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922322_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922322: C129_G4_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129565">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129565</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922322</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922322</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313420" alias="GSM5922323_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313420</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922323_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922323: C129_G5_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129566">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129566</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922323</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922323</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313421" alias="GSM5922324_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313421</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922324_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922324: C129_G6_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129567">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129567</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922324</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922324</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313422" alias="GSM5922325_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313422</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922325_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922325: C129_G7_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129569">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129569</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922325</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922325</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313423" alias="GSM5922326_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313423</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922326_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922326: C129_G8_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129568">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129568</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922326</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922326</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313424" alias="GSM5922327_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313424</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922327_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922327: C129_H1_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129570">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129570</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922327</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922327</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313425" alias="GSM5922328_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313425</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922328_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922328: C129_H10_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129572">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129572</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922328</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922328</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313426" alias="GSM5922329_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313426</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922329_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922329: C129_H11_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129571">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129571</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922329</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922329</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313427" alias="GSM5922330_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313427</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922330_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922330: C129_H12_L1_38wUW_RepN_MBULK; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129573">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129573</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922330</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922330</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313428" alias="GSM5922331_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313428</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922331_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922331: C129_H2_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129574">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129574</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922331</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922331</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313429" alias="GSM5922044_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313429</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922044_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922044: C114_D10_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129575">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129575</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922044</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922044</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313430" alias="GSM5922045_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313430</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922045_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922045: C114_D11_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129576">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129576</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922045</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922045</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313431" alias="GSM5922046_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313431</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922046_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922046: C114_D3_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129577">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129577</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922046</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922046</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313432" alias="GSM5922047_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313432</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922047_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922047: C114_D7_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129578">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129578</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922047</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922047</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313433" alias="GSM5922048_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313433</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922048_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922048: C114_D8_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129579">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129579</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922048</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922048</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313434" alias="GSM5922049_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313434</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922049_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922049: C114_D9_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129580">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129580</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922049</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922049</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313435" alias="GSM5922050_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313435</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922050_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922050: C114_E1_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129581">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129581</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922050</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922050</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313436" alias="GSM5922051_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313436</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922051_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922051: C114_E1_L1_38w_RepI_IDTILL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129582">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129582</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922051</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922051</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313437" alias="GSM5922052_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313437</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922052_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922052: C114_E2_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129583">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129583</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922052</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922052</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313438" alias="GSM5922053_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313438</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922053_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922053: C114_E2_L1_38w_RepI_IDTILL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129584">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129584</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922053</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922053</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313439" alias="GSM5922054_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313439</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922054_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922054: C114_E3_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129585">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129585</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922054</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922054</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313440" alias="GSM5922055_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313440</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922055_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922055: C114_E3_L1_38w_RepI__IDTILL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129587">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129587</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922055</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922055</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313441" alias="GSM5922056_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313441</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922056_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922056: C114_E4_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129586">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129586</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922056</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922056</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313442" alias="GSM5922057_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313442</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922057_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922057: C114_E4_L1_38w_RepI__IDTILL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129588">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129588</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922057</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922057</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313443" alias="GSM5922058_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313443</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922058_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922058: C114_E5_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129589">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129589</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922058</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922058</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313444" alias="GSM5922059_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313444</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922059_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922059: C114_E6_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129590">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129590</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922059</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922059</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313445" alias="GSM5922092_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313445</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922092_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922092: C118_B11_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129591">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129591</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922092</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922092</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313446" alias="GSM5922093_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313446</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922093_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922093: C118_B12_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129594">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129594</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922093</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922093</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313447" alias="GSM5922094_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313447</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922094_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922094: C118_B3_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129593">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129593</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922094</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922094</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313448" alias="GSM5922095_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313448</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922095_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922095: C118_B4_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129592">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129592</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922095</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922095</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313449" alias="GSM5922096_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313449</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922096_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922096: C118_B7_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129595">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129595</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922096</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922096</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313450" alias="GSM5922097_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313450</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922097_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922097: C118_B9_L1_38w_RepI; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129596">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129596</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922097</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922097</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313451" alias="GSM5922098_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313451</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922098_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922098: C119_A10_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129597">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129597</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922098</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922098</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313452" alias="GSM5922099_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313452</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922099_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922099: C119_A11_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129599">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129599</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922099</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922099</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313453" alias="GSM5922100_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313453</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922100_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922100: C119_A12_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129598">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129598</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922100</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922100</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313454" alias="GSM5922101_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313454</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922101_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922101: C119_A2_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129600">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129600</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922101</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922101</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313455" alias="GSM5922102_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313455</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922102_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922102: C119_A3_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129601">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129601</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922102</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922102</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313456" alias="GSM5922103_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313456</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922103_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922103: C119_A4_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129602">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129602</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922103</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922103</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313457" alias="GSM5922104_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313457</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922104_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922104: C119_A6_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129603">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129603</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922104</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922104</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313458" alias="GSM5922105_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313458</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922105_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922105: C119_A7_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129604">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129604</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922105</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922105</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313459" alias="GSM5922106_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313459</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922106_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922106: C119_A8_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129605">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129605</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922106</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922106</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313460" alias="GSM5922107_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313460</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922107_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922107: C119_A9_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129606">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129606</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922107</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922107</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313461" alias="GSM5922156_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313461</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922156_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922156: C119_G12_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129607">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129607</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922156</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922156</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313462" alias="GSM5922157_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313462</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922157_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922157: C119_G2_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129608">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129608</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922157</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922157</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313463" alias="GSM5922158_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313463</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922158_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922158: C119_G3_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129609">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129609</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922158</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922158</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313464" alias="GSM5922159_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313464</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922159_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922159: C119_G4_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129610">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129610</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922159</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922159</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313465" alias="GSM5922160_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313465</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922160_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922160: C119_G6_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129611">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129611</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922160</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922160</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313466" alias="GSM5922161_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313466</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922161_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922161: C119_G7_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129612">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129612</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922161</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922161</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313467" alias="GSM5922162_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313467</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922162_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922162: C119_G8_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129613">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129613</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922162</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922162</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313468" alias="GSM5922163_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313468</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922163_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922163: C119_G9_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129615">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129615</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922163</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922163</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313469" alias="GSM5922164_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313469</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922164_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922164: C119_H1_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129614">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129614</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922164</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922164</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313470" alias="GSM5922165_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313470</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922165_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922165: C119_H10_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129616">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129616</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922165</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922165</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313471" alias="GSM5922166_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313471</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922166_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922166: C119_H11_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129618">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129618</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922166</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922166</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313472" alias="GSM5922167_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313472</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922167_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922167: C119_H12_L1_38w_RepL_MBULK; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129617">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129617</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922167</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922167</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313473" alias="GSM5922168_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313473</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922168_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922168: C119_H2_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129619">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129619</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922168</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922168</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313474" alias="GSM5922169_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313474</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922169_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922169: C119_H6_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129620">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129620</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922169</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922169</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313475" alias="GSM5922170_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313475</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922170_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922170: C119_H7_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129621">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129621</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922170</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922170</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313476" alias="GSM5922171_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313476</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922171_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922171: C119_H8_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129622">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129622</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922171</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922171</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313477" alias="GSM5922268_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313477</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922268_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922268: C129_B2_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129623">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129623</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922268</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922268</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313478" alias="GSM5922269_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313478</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922269_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922269: C129_B3_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129624">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129624</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922269</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922269</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313479" alias="GSM5922270_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313479</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922270_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922270: C129_B4_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129625">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129625</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922270</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922270</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313480" alias="GSM5922271_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313480</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922271_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922271: C129_B5_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129626">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129626</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922271</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922271</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313481" alias="GSM5922272_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313481</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922272_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922272: C129_B6_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129627">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129627</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922272</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922272</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313482" alias="GSM5922273_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313482</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922273_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922273: C129_B7_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129628">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129628</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922273</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922273</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313483" alias="GSM5922274_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313483</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922274_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922274: C129_B8_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129629">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129629</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922274</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922274</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313484" alias="GSM5922275_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313484</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922275_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922275: C129_C1_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129630">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129630</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922275</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922275</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313485" alias="GSM5922276_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313485</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922276_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922276: C129_C10_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129631">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129631</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922276</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922276</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313486" alias="GSM5922277_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313486</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922277_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922277: C129_C11_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129632">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129632</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922277</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922277</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313487" alias="GSM5922278_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313487</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922278_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922278: C129_C12_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129633">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129633</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922278</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922278</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313488" alias="GSM5922279_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313488</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922279_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922279: C129_C2_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129634">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129634</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922279</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922279</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313489" alias="GSM5922280_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313489</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922280_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922280: C129_C3_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129635">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129635</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922280</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922280</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313490" alias="GSM5922281_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313490</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922281_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922281: C129_C4_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129636">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129636</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922281</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922281</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313491" alias="GSM5922282_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313491</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922282_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922282: C129_C5_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129637">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129637</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922282</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922282</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313492" alias="GSM5922283_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313492</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922283_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922283: C129_C6_L1_38wUW_RepN; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129638">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129638</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922283</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922283</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313493" alias="GSM5922108_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313493</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922108_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922108: C119_B10_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129639">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129639</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922108</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922108</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313494" alias="GSM5922109_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313494</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922109_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922109: C119_B11_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129640">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129640</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922109</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922109</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313495" alias="GSM5922110_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313495</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922110_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922110: C119_B12_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129641">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129641</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922110</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922110</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313496" alias="GSM5922111_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313496</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922111_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922111: C119_B2_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129642">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129642</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922111</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922111</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313497" alias="GSM5922112_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313497</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922112_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922112: C119_B3_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129643">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129643</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922112</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922112</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX14313498" alias="GSM5922113_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX14313498</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5922113_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5922113: C119_B4_L1_38w_RepL; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP361807">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP361807</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA811146</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12129644">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12129644</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5922113</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5922113</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>Flow citometry was used to sort tomato positive epidermal cells Full length single cell RNA-seq was performed using a modified version of the Smart-seq2 protocol. Briefly, individual cells are sorted into 96 well plates containing lysis buffer in presence of RNase inhibitor, dNTPs and OligodT. Reverse transcription of the polyadenylated RNA will be performed with SuperScriptII and Template Switching Oligos. The resulting cDNA will be amplified with 25 cycles of PCR and libraries will be prepared for sequencing with standard NexteraXT Illumina protocol. Libraries were sequenced on Illumina NextSeq 500 System (single-end 75bp reads).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
