<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX18700902" alias="GSM6833440_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700902</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833440_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833440: gRNA IL2primary popUN rep1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16141977">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16141977</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833440</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833440</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700903" alias="GSM6833441_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700903</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833441_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833441: gRNA IL2primary popUN rep2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16141978">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16141978</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833441</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833441</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700904" alias="GSM6833442_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700904</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833442_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833442: gRNA IL2primary popNEG rep1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16141979">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16141979</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833442</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833442</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700905" alias="GSM6833443_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700905</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833443_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833443: gRNA IL2primary popNEG rep2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16141980">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16141980</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833443</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833443</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700906" alias="GSM6833444_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700906</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833444_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833444: gRNA IL2primary popNEG rep3; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16141981">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16141981</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833444</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833444</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700907" alias="GSM6833445_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700907</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833445_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833445: gRNA IL2primary popIL2 rep1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16141982">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16141982</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833445</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833445</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700908" alias="GSM6833446_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700908</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833446_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833446: gRNA IL2primary popIL2 rep2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16141983">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16141983</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833446</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833446</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700909" alias="GSM6833447_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700909</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833447_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833447: gRNA IL2primary popIL2 rep3; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16141984">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16141984</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833447</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833447</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700910" alias="GSM6833448_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700910</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833448_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833448: gRNA IL2primary popDP rep1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16141985">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16141985</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833448</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833448</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700911" alias="GSM6833449_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700911</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833449_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833449: gRNA IL2primary popDP rep2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16141986">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16141986</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833449</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833449</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700912" alias="GSM6833450_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700912</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833450_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833450: gRNA IL2primary popDP rep3; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16141987">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16141987</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833450</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833450</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700913" alias="GSM6833451_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700913</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833451_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833451: gRNA IL2primary popIFNG rep1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16141988">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16141988</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833451</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833451</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700914" alias="GSM6833452_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700914</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833452_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833452: gRNA IL2primary popIFNG rep2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16141989">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16141989</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833452</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833452</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700915" alias="GSM6833453_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700915</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833453_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833453: gRNA IL2primary popIFNG rep3; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16141990">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16141990</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833453</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833453</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700916" alias="GSM6833454_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700916</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833454_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833454: gRNA IFNG popUN rep1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16141991">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16141991</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833454</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833454</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700917" alias="GSM6833455_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700917</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833455_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833455: gRNA IFNG popUN rep2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16141992">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16141992</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833455</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833455</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700918" alias="GSM6833456_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700918</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833456_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833456: gRNA IFNG popUN rep3; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16141993">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16141993</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833456</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833456</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700919" alias="GSM6833457_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700919</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833457_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833457: gRNA IFNG popNEG rep1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16141994">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16141994</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833457</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833457</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700920" alias="GSM6833458_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700920</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833458_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833458: gRNA IFNG popNEG rep2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16141995">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16141995</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833458</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833458</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700921" alias="GSM6833459_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700921</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833459_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833459: gRNA IFNG popNEG rep3; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16141997">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16141997</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833459</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833459</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700922" alias="GSM6833460_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700922</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833460_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833460: gRNA IFNG popIL2 rep1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16141996">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16141996</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833460</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833460</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700923" alias="GSM6833461_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700923</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833461_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833461: gRNA IFNG popIL2 rep2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16141998">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16141998</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833461</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833461</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700924" alias="GSM6833462_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700924</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833462_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833462: gRNA IFNG popIL2 rep3; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16141999">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16141999</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833462</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833462</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700925" alias="GSM6833463_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700925</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833463_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833463: gRNA IFNG popDP rep1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16142000">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16142000</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833463</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833463</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700926" alias="GSM6833464_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700926</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833464_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833464: gRNA IFNG popDP rep2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16142001">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16142001</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833464</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833464</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700927" alias="GSM6833465_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700927</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833465_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833465: gRNA IFNG popDP rep3; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16142002">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16142002</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833465</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833465</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700928" alias="GSM6833466_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700928</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833466_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833466: gRNA IFNG popIFNG rep1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16142003">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16142003</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833466</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833466</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700929" alias="GSM6833467_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700929</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833467_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833467: gRNA IFNG popIFNG rep2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16142004">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16142004</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833467</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833467</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700930" alias="GSM6833468_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700930</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833468_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833468: gRNA IFNG popIFNG rep3; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16142005">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16142005</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833468</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833468</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700931" alias="GSM6833469_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700931</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833469_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833469: gRNA IL2validation popUN rep1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16142006">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16142006</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833469</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833469</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700932" alias="GSM6833470_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700932</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833470_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833470: gRNA IL2validation popUN rep2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16142007">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16142007</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833470</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833470</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700933" alias="GSM6833471_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700933</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833471_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833471: gRNA IL2validation popUN rep3; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16142008">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16142008</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833471</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833471</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700934" alias="GSM6833472_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700934</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833472_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833472: gRNA IL2validation popNEG rep1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16142009">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16142009</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833472</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833472</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700935" alias="GSM6833473_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700935</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833473_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833473: gRNA IL2validation popNEG rep2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16142010">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16142010</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833473</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833473</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700936" alias="GSM6833474_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700936</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833474_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833474: gRNA IL2validation popNEG rep3; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16142011">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16142011</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833474</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833474</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700937" alias="GSM6833475_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700937</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833475_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833475: gRNA IL2validation popIL2 rep1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16142012">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16142012</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833475</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833475</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700938" alias="GSM6833476_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700938</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833476_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833476: gRNA IL2validation popIL2 rep2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16142013">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16142013</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833476</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833476</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18700939" alias="GSM6833477_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18700939</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6833477_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6833477: gRNA IL2validation popIL2 rep3; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP413083">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP413083</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA912209</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16142014">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16142014</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6833477</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6833477</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were sorted by FACS for live cells and for the cell populations expressing the constructs of interest. Genomic DNA (gDNA) was extracted from sorted cells for different cytokine populations using Quick-DNA Miniprep kit (Zymo) or a custom precipitation-based gDNA extraction protocol. gRNA enrichment libraries were prepared from gDNA using a 3-step custom PCR protocol using gRNA-specific nested primers.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
