<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX18273072" alias="GSM6732454_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273072</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732454_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732454: Patient 3 CD8+ [Pt03_CD8 RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765561">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765561</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732454</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732454</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273073" alias="GSM6732455_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273073</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732455_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732455: Patient 7 CD4+ [Pt07_CD4 RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765562">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765562</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732455</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732455</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273074" alias="GSM6732480_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273074</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732480_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732480: Patient 21 CD8+ [Pt21_CD8 RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765563">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765563</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732480</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732480</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273075" alias="GSM6732481_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273075</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732481_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732481: Patient 21 CD4+CD8+ [Pt21_DP RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765564">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765564</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732481</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732481</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273076" alias="GSM6732482_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273076</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732482_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732482: Patient 22 CD4+ [Pt22_CD4 RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765565">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765565</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732482</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732482</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273077" alias="GSM6732483_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273077</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732483_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732483: Patient 22 CD8+ [Pt22_CD8 RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765566">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765566</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732483</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732483</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273078" alias="GSM6732484_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273078</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732484_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732484: Patient 22 CD4+CD8+ [Pt22_DP RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765567">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765567</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732484</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732484</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273079" alias="GSM6732485_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273079</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732485_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732485: Patient 23 CD4+ [Pt23_CD4 RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765568">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765568</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732485</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732485</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273080" alias="GSM6732487_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273080</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732487_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732487: Patient 24 CD8+ [Pt24_CD8 RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765569">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765569</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732487</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732487</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273081" alias="GSM6732486_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273081</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732486_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732486: Patient 24 CD4+ [Pt24_CD4 RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765570">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765570</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732486</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732486</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273082" alias="GSM6732456_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273082</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732456_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732456: Patient 7 CD8+ [Pt07_CD8 RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765571">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765571</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732456</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732456</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273083" alias="GSM6732457_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273083</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732457_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732457: Patient 7 CD4+CD8+ [Pt07_DP RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765572">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765572</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732457</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732457</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273084" alias="GSM6732458_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273084</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732458_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732458: Patient 8 CD4+ [Pt08_CD4 RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765573">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765573</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732458</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732458</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273085" alias="GSM6732459_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273085</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732459_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732459: Patient 8 CD4+CD8+ [Pt08_DP RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765574">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765574</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732459</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732459</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273086" alias="GSM6732460_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273086</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732460_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732460: Patient 9 CD4+ [Pt09_CD4 RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765575">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765575</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732460</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732460</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273087" alias="GSM6732461_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273087</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732461_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732461: Patient 9 CD8+ [Pt09_CD8 RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765576">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765576</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732461</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732461</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273088" alias="GSM6732462_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273088</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732462_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732462: Patient 9 CD4+CD8+ [Pt09_DP RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765577">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765577</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732462</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732462</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273089" alias="GSM6732463_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273089</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732463_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732463: Patient 11 CD4+ [Pt11_CD4 RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765578">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765578</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732463</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732463</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273090" alias="GSM6732464_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273090</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732464_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732464: Patient 11 CD8+ [Pt11_CD8 RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765579">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765579</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732464</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732464</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273091" alias="GSM6732465_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273091</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732465_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732465: Patient 11 CD4+CD8+ [Pt11_DP RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765580">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765580</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732465</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732465</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273092" alias="GSM6732466_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273092</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732466_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732466: Patient 14 CD4+ [Pt14_CD4 RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765581">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765581</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732466</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732466</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273093" alias="GSM6732467_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273093</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732467_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732467: Patient 14 CD8+ [Pt14_CD8 RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765582">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765582</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732467</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732467</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273094" alias="GSM6732468_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273094</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732468_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732468: Patient 15 CD4+ [Pt15_CD4 RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765583">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765583</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732468</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732468</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273095" alias="GSM6732469_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273095</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732469_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732469: Patient 15 CD4+CD8+ [Pt15_DP RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765584">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765584</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732469</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732469</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273096" alias="GSM6732470_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273096</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732470_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732470: Patient 16 CD4+ [Pt16_CD4 RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765585">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765585</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732470</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732470</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273097" alias="GSM6732471_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273097</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732471_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732471: Patient 16 CD8+ [Pt16_CD8 RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765586">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765586</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732471</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732471</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273098" alias="GSM6732472_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273098</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732472_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732472: Patient 16 CD4+CD8+ [Pt16_DP RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765587">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765587</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732472</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732472</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273099" alias="GSM6732473_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273099</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732473_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732473: Patient 18 CD4+ [Pt18_CD4 RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765588">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765588</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732473</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732473</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273100" alias="GSM6732474_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273100</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732474_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732474: Patient 18 CD8+ [Pt18_CD8 RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765589">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765589</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732474</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732474</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273101" alias="GSM6732475_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273101</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732475_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732475: Patient 18 CD4+CD8+ [Pt18_DP RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765590">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765590</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732475</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732475</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273102" alias="GSM6732476_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273102</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732476_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732476: Patient 20 CD4+ [Pt20_CD4 RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765591">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765591</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732476</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732476</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273103" alias="GSM6732477_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273103</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732477_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732477: Patient 20 CD8+ [Pt20_CD8 RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765592">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765592</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732477</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732477</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273104" alias="GSM6732478_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273104</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732478_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732478: Patient 20 CD4+CD8+ [Pt20_DP RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765593">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765593</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732478</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732478</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18273105" alias="GSM6732479_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18273105</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6732479_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6732479: Patient 21 CD4+ [Pt21_CD4 RNA-seq]; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408054">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408054</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901910</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15765594">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15765594</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6732479</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6732479</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was extracted from CD4+ and CD8+ sorted TIL with the Qiagen RNEasy Mini Kit. 100ng of RNA was used to generate cDNA and a strand-specific library following the manufacturer's protocol (NuGEN Technologies, Inc., San Carlos, CA). These libraries were then sequenced on the Illumina NextSeq 500 v2 sequencer with a 75-base paired-end run in order to generate 30-40 million read pairs per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
