<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX18379097" alias="GSM6756589_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379097</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756589_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756589: 190712_media_M5_Diff_S2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15864972">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15864972</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756589</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756589</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379098" alias="GSM6756590_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379098</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756590_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756590: 190712_media_M5_Stem_S1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15864973">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15864973</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756590</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756590</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379099" alias="GSM6756591_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379099</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756591_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756591: 190712_media_M5_Stem_S2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15864974">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15864974</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756591</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756591</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379100" alias="GSM6756592_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379100</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756592_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756592: 190712_media_M5_Unsorted_S1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15864975">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15864975</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756592</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756592</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379101" alias="GSM6756593_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379101</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756593_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756593: 190712_media_M5_Unsorted_S2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15864976">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15864976</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756593</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756593</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379102" alias="GSM6756594_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379102</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756594_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756594: 190712_media_M6_Diff_S1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15864977">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15864977</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756594</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756594</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379103" alias="GSM6756595_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379103</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756595_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756595: 190712_media_M6_Diff_S2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15864978">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15864978</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756595</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756595</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379104" alias="GSM6756596_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379104</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756596_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756596: 190712_media_M6_Stem_S1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15864979">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15864979</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756596</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756596</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379105" alias="GSM6756597_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379105</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756597_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756597: 190712_media_M6_Stem_S2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15864980">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15864980</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756597</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756597</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379106" alias="GSM6756598_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379106</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756598_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756598: 190712_media_M6_Unsorted_S1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15864981">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15864981</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756598</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756598</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379107" alias="GSM6756599_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379107</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756599_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756599: 190712_media_M6_Unsorted_S2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15864982">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15864982</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756599</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756599</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379108" alias="GSM6756600_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379108</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756600_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756600: 190712_media_M7_Diff_S1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15864983">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15864983</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756600</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756600</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379109" alias="GSM6756601_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379109</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756601_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756601: 190712_media_M7_Diff_S2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15864984">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15864984</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756601</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756601</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379110" alias="GSM6756602_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379110</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756602_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756602: 190712_media_M7_Stem_S1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15864985">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15864985</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756602</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756602</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379111" alias="GSM6756603_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379111</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756603_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756603: 190712_media_M7_Stem_S2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15864986">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15864986</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756603</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756603</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379112" alias="GSM6756604_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379112</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756604_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756604: 190712_media_M7_Unsorted_S1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15864987">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15864987</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756604</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756604</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379113" alias="GSM6756605_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379113</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756605_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756605: 190712_media_M7_Unsorted_S2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15864988">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15864988</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756605</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756605</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379114" alias="GSM6756562_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379114</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756562_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756562: 190712_media_Plasmid; Escherichia coli; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15864989">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15864989</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756562</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756562</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>OTHER</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379115" alias="GSM6756563_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379115</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756563_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756563: 190712_media_Lentivirus; Lentivirus; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15864990">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15864990</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756563</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756563</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>OTHER</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379116" alias="GSM6756564_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379116</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756564_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756564: 190712_media_M1_Diff_S1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15864991">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15864991</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756564</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756564</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379117" alias="GSM6756565_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379117</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756565_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756565: 190712_media_M1_Diff_S2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15864992">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15864992</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756565</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756565</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379118" alias="GSM6756566_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379118</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756566_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756566: 190712_media_M1_Stem_S1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15864993">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15864993</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756566</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756566</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379119" alias="GSM6756567_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379119</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756567_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756567: 190712_media_M1_Stem_S2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15864994">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15864994</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756567</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756567</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379120" alias="GSM6756568_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379120</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756568_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756568: 190712_media_M1_Unsorted_S1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15864995">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15864995</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756568</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756568</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379121" alias="GSM6756569_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379121</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756569_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756569: 190712_media_M1_Unsorted_S2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15864996">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15864996</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756569</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756569</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379122" alias="GSM6756570_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379122</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756570_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756570: 190712_media_M2_Diff_S1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15864997">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15864997</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756570</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756570</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379123" alias="GSM6756571_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379123</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756571_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756571: 190712_media_M2_Diff_S2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15864998">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15864998</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756571</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756571</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379124" alias="GSM6756572_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379124</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756572_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756572: 190712_media_M2_Stem_S1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15864999">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15864999</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756572</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756572</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379125" alias="GSM6756573_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379125</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756573_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756573: 190712_media_M2_Stem_S2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15865000">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15865000</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756573</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756573</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379126" alias="GSM6756574_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379126</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756574_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756574: 190712_media_M2_Unsorted_S1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15865001">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15865001</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756574</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756574</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379127" alias="GSM6756575_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379127</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756575_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756575: 190712_media_M2_Unsorted_S2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15865002">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15865002</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756575</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756575</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379128" alias="GSM6756576_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379128</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756576_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756576: 190712_media_M3_Diff_S1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15865003">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15865003</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756576</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756576</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379129" alias="GSM6756577_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379129</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756577_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756577: 190712_media_M3_Diff_S2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15865004">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15865004</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756577</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756577</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379130" alias="GSM6756578_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379130</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756578_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756578: 190712_media_M3_Stem_S1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15865005">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15865005</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756578</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756578</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379131" alias="GSM6756579_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379131</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756579_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756579: 190712_media_M3_Stem_S2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15865006">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15865006</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756579</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756579</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379132" alias="GSM6756580_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379132</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756580_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756580: 190712_media_M3_Unsorted_S1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15865007">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15865007</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756580</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756580</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379133" alias="GSM6756581_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379133</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756581_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756581: 190712_media_M3_Unsorted_S2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15865008">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15865008</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756581</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756581</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379134" alias="GSM6756582_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379134</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756582_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756582: 190712_media_M4_Diff_S1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15865009">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15865009</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756582</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756582</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379135" alias="GSM6756583_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379135</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756583_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756583: 190712_media_M4_Diff_S2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15865010">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15865010</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756583</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756583</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379136" alias="GSM6756584_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379136</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756584_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756584: 190712_media_M4_Stem_S1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15865011">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15865011</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756584</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756584</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379137" alias="GSM6756585_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379137</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756585_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756585: 190712_media_M4_Stem_S2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15865012">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15865012</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756585</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756585</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379138" alias="GSM6756586_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379138</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756586_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756586: 190712_media_M4_Unsorted_S1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15865013">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15865013</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756586</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756586</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379139" alias="GSM6756587_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379139</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756587_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756587: 190712_media_M4_Unsorted_S2; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15865014">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15865014</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756587</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756587</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18379140" alias="GSM6756588_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18379140</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6756588_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6756588: 190712_media_M5_Diff_S1; Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP409826">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409826</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905451</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15865015">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15865015</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6756588</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6756588</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Lentivirus RNA was extracted using the QIAmp Viral RNA Mini Kit (Qiagen 52906). Genomic DNA was extracted using the Quick-DNA Midiprep Plus Kit (Zymo D4075) Lentivirus RNA was reverse transcribed using the qScript Flex cDNA Kit (VWR 95049-100) with a custom primer (see Methods). Libraries were prepared by PCR amplification of TF barcodes using custom primers (see Methods)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 550</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
