<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="GSM3561456" accession="SRX5246885">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5246885</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3561456</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3561456: SMARCA4 ChIP-Seq (NSC); Homo sapiens; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP179040" refname="GSE125033">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP179040</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4249120">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4249120</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3561456</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromatin immunoprecipitation was done as described previously (Ding et al., 2015) using 20 μl of ChIP-grade SMARCA4 (abcam 110641). DNA was fragmented to 200-500bp with a Covaris water-bath sonicator before the IP. DNA was purified and eluted using a PCR purification kit (Qiagen) in 30 μl HPLC-grade water. ChIP-Seq libraries were prepared for sequencing using standard Illumina protocols.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303561456</ID>
          <LABEL>GSM3561456</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3561456</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3561457" accession="SRX5246886">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5246886</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3561457</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3561457: Input ChIP-Seq (NSC); Homo sapiens; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP179040" refname="GSE125033">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP179040</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4249121">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4249121</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3561457</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total genomic DNA was fragmented to 200-500bp with a Covaris water-bath sonicator. DNA was purified and eluted using a PCR purification kit (Qiagen) in 30 μl HPLC-grade water. ChIP-Seq libraries were prepared for sequencing using standard Illumina protocols.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303561457</ID>
          <LABEL>GSM3561457</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3561457</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3561458" accession="SRX5246887">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5246887</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3561458</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3561458: HSPC CD34+ day 12 RNA-Seq; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP179040" refname="GSE125033">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP179040</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4249122">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4249122</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3561458</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>For RNA extraction, typically 1-2 million cells were pooled down. Total RNA extraction was performed with the RNeasy Mini kit (Qiagen) according to manufacturer's instructions. To avoid contamination with genomic DNA an on-column DNase I digest was included as part of the RNase Mini kit protocol. RNA libraries were prepared for sequencing using standard Illumina protocols.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303561458</ID>
          <LABEL>GSM3561458</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3561458</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3561459" accession="SRX5246888">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5246888</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3561459</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3561459: HSPC CD34+ day 22 RNA-Seq; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP179040" refname="GSE125033">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP179040</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4249123">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4249123</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3561459</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>For RNA extraction, typically 1-2 million cells were pooled down. Total RNA extraction was performed with the RNeasy Mini kit (Qiagen) according to manufacturer's instructions. To avoid contamination with genomic DNA an on-column DNase I digest was included as part of the RNase Mini kit protocol. RNA libraries were prepared for sequencing using standard Illumina protocols.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303561459</ID>
          <LABEL>GSM3561459</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3561459</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3561460" accession="SRX5246889">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5246889</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3561460</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3561460: iPSC RNA-Seq; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP179040" refname="GSE125033">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP179040</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4249124">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4249124</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3561460</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>For RNA extraction, typically 1-2 million cells were pooled down. Total RNA extraction was performed with the RNeasy Mini kit (Qiagen) according to manufacturer's instructions. To avoid contamination with genomic DNA an on-column DNase I digest was included as part of the RNase Mini kit protocol. RNA libraries were prepared for sequencing using standard Illumina protocols.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303561460</ID>
          <LABEL>GSM3561460</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3561460</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3561461" accession="SRX5246890">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5246890</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3561461</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3561461: NSC RNA-Seq; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP179040" refname="GSE125033">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP179040</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4249125">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4249125</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3561461</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>For RNA extraction, typically 1-2 million cells were pooled down. Total RNA extraction was performed with the RNeasy Mini kit (Qiagen) according to manufacturer's instructions. To avoid contamination with genomic DNA an on-column DNase I digest was included as part of the RNase Mini kit protocol. RNA libraries were prepared for sequencing using standard Illumina protocols.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303561461</ID>
          <LABEL>GSM3561461</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3561461</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3561462" accession="SRX5246891">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5246891</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3561462</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3561462: HSPC CD34+ shRNA screen (day 2); Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP179040" refname="GSE125033">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP179040</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4249126">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4249126</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3561462</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells carrying shRNAs were sorted according to the given sorting criteria and DNA fragments containing the shRNA barcodes were PCR amplified from genomic DNA. Libraries were prepared for sequencing using standard Illumina protocols for PCR amplicons.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303561462</ID>
          <LABEL>GSM3561462</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3561462</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3561463" accession="SRX5246892">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5246892</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3561463</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3561463: HSPC CD34+ shRNA screen (day 12); Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP179040" refname="GSE125033">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP179040</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4249127">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4249127</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3561463</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells carrying shRNAs were sorted according to the given sorting criteria and DNA fragments containing the shRNA barcodes were PCR amplified from genomic DNA. Libraries were prepared for sequencing using standard Illumina protocols for PCR amplicons.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303561463</ID>
          <LABEL>GSM3561463</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3561463</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3561464" accession="SRX5246893">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5246893</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3561464</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3561464: HSPC CD34+ shRNA screen (day 22); Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP179040" refname="GSE125033">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP179040</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4249128">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4249128</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3561464</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells carrying shRNAs were sorted according to the given sorting criteria and DNA fragments containing the shRNA barcodes were PCR amplified from genomic DNA. Libraries were prepared for sequencing using standard Illumina protocols for PCR amplicons.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303561464</ID>
          <LABEL>GSM3561464</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3561464</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3561465" accession="SRX5246894">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5246894</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3561465</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3561465: HSPC CD34- shRNA screen (day 12); Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP179040" refname="GSE125033">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP179040</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4249129">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4249129</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3561465</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells carrying shRNAs were sorted according to the given sorting criteria and DNA fragments containing the shRNA barcodes were PCR amplified from genomic DNA. Libraries were prepared for sequencing using standard Illumina protocols for PCR amplicons.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303561465</ID>
          <LABEL>GSM3561465</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3561465</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3561466" accession="SRX5246895">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5246895</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3561466</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3561466: HSPC CD34- shRNA screen (day 22); Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP179040" refname="GSE125033">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP179040</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4249130">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4249130</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3561466</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells carrying shRNAs were sorted according to the given sorting criteria and DNA fragments containing the shRNA barcodes were PCR amplified from genomic DNA. Libraries were prepared for sequencing using standard Illumina protocols for PCR amplicons.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303561466</ID>
          <LABEL>GSM3561466</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3561466</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3561467" accession="SRX5246896">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5246896</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3561467</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3561467: NSC shRNA screen (day 2); Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP179040" refname="GSE125033">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP179040</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4249131">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4249131</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3561467</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells carrying shRNAs were sorted according to the given sorting criteria and DNA fragments containing the shRNA barcodes were PCR amplified from genomic DNA. Libraries were prepared for sequencing using standard Illumina protocols for PCR amplicons.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303561467</ID>
          <LABEL>GSM3561467</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3561467</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3561468" accession="SRX5246897">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5246897</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3561468</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3561468: NSC shRNA screen (day 12); Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP179040" refname="GSE125033">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP179040</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4249132">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4249132</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3561468</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells carrying shRNAs were sorted according to the given sorting criteria and DNA fragments containing the shRNA barcodes were PCR amplified from genomic DNA. Libraries were prepared for sequencing using standard Illumina protocols for PCR amplicons.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303561468</ID>
          <LABEL>GSM3561468</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3561468</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3561469" accession="SRX5246898">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5246898</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3561469</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3561469: NSC shRNA screen (day 22); Homo sapiens; OTHER</TITLE>
    <STUDY_REF accession="SRP179040" refname="GSE125033">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP179040</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4249133">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4249133</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3561469</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells carrying shRNAs were sorted according to the given sorting criteria and DNA fragments containing the shRNA barcodes were PCR amplified from genomic DNA. Libraries were prepared for sequencing using standard Illumina protocols for PCR amplicons.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303561469</ID>
          <LABEL>GSM3561469</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3561469</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
</EXPERIMENT_SET>
