<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX18319180" alias="GSM6743921_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18319180</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6743921_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6743921: "spike for sgEts1_1"_ day 7 1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408728">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408728</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903380</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15809627">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15809627</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6743921</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6743921</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC SINGLE CELL</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>CD8+ OT-I T cells were sorted from the dual-color transfer system at day 7 post adoptive transfer from B16-OVA tumor and loaded onto  the Chromium Controller according to their respective cell counts to target 9000 single cell GEMs (gel beads in emulsion) per sample. Libraries were prepared using the Chromium Single Cell 3' v3 Library and Gel Bead Kit (10x Genomics)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18319181" alias="GSM6743922_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18319181</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6743922_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6743922: "spike for sgEts1_1"_ day 7 2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408728">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408728</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903380</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15809628">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15809628</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6743922</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6743922</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC SINGLE CELL</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>CD8+ OT-I T cells were sorted from the dual-color transfer system at day 7 post adoptive transfer from B16-OVA tumor and loaded onto  the Chromium Controller according to their respective cell counts to target 9000 single cell GEMs (gel beads in emulsion) per sample. Libraries were prepared using the Chromium Single Cell 3' v3 Library and Gel Bead Kit (10x Genomics)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18319182" alias="GSM6743923_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18319182</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6743923_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6743923: sgEts1_1_day 7 1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408728">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408728</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903380</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15809629">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15809629</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6743923</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6743923</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC SINGLE CELL</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>CD8+ OT-I T cells were sorted from the dual-color transfer system at day 7 post adoptive transfer from B16-OVA tumor and loaded onto  the Chromium Controller according to their respective cell counts to target 9000 single cell GEMs (gel beads in emulsion) per sample. Libraries were prepared using the Chromium Single Cell 3' v3 Library and Gel Bead Kit (10x Genomics)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18319183" alias="GSM6743924_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18319183</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6743924_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6743924: sgEts1_1_day 7 2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408728">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408728</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903380</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15809630">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15809630</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6743924</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6743924</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC SINGLE CELL</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>CD8+ OT-I T cells were sorted from the dual-color transfer system at day 7 post adoptive transfer from B16-OVA tumor and loaded onto  the Chromium Controller according to their respective cell counts to target 9000 single cell GEMs (gel beads in emulsion) per sample. Libraries were prepared using the Chromium Single Cell 3' v3 Library and Gel Bead Kit (10x Genomics)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
