<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="GSM3021797" accession="SRX3741065">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3741065</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3021797</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3021797: RNA-seq NOTCH2NL WT rep 1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP133438" refname="GSE111082">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP133438</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2997737">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2997737</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3021797</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>Human organoid samples: Pools of 5-10 organoids per replicate were harvested in TRIzol at day 28 for RNA extraction. Mouse organoid samples: Three pools of 16 organoids were isolated in TRIzol after 6 days of differentiation for EV and NOTCH2NL-Sh_T197I organoids. RNA was isolated using standard TRIzol protocol, followed by DNaseI treatment (Rochte) and column purification (Zymo RNA clean and concentrator 5). mRNA was isolated from total RNA using polyA selection Dynabeads mRNA DIRECT Micro Purification Kit (Thermofisher). Library was prepared using strand-specific Ion Total RNA-seq Kit v2 (Thermofisher) and Ion Xpress RNA-seq Barcode 1-16 (Thermofisher) to label different samples.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303021797</ID>
          <LABEL>GSM3021797</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3021797</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3021798" accession="SRX3741066">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3741066</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3021798</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3021798: RNA-seq NOTCH2NL WT rep 2; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP133438" refname="GSE111082">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP133438</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2997738">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2997738</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3021798</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>Human organoid samples: Pools of 5-10 organoids per replicate were harvested in TRIzol at day 28 for RNA extraction. Mouse organoid samples: Three pools of 16 organoids were isolated in TRIzol after 6 days of differentiation for EV and NOTCH2NL-Sh_T197I organoids. RNA was isolated using standard TRIzol protocol, followed by DNaseI treatment (Rochte) and column purification (Zymo RNA clean and concentrator 5). mRNA was isolated from total RNA using polyA selection Dynabeads mRNA DIRECT Micro Purification Kit (Thermofisher). Library was prepared using strand-specific Ion Total RNA-seq Kit v2 (Thermofisher) and Ion Xpress RNA-seq Barcode 1-16 (Thermofisher) to label different samples.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303021798</ID>
          <LABEL>GSM3021798</LABEL>
        </XREF_LINK>
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    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3021798</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3021799" accession="SRX3741067">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3741067</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3021799</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3021799: RNA-seq NOTCH2NL WT rep 3; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP133438" refname="GSE111082">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP133438</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2997739">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2997739</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3021799</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>Human organoid samples: Pools of 5-10 organoids per replicate were harvested in TRIzol at day 28 for RNA extraction. Mouse organoid samples: Three pools of 16 organoids were isolated in TRIzol after 6 days of differentiation for EV and NOTCH2NL-Sh_T197I organoids. RNA was isolated using standard TRIzol protocol, followed by DNaseI treatment (Rochte) and column purification (Zymo RNA clean and concentrator 5). mRNA was isolated from total RNA using polyA selection Dynabeads mRNA DIRECT Micro Purification Kit (Thermofisher). Library was prepared using strand-specific Ion Total RNA-seq Kit v2 (Thermofisher) and Ion Xpress RNA-seq Barcode 1-16 (Thermofisher) to label different samples.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303021799</ID>
          <LABEL>GSM3021799</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3021799</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3021800" accession="SRX3741068">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3741068</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3021800</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3021800: RNA-seq NOTCH2NL KO rep 1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP133438" refname="GSE111082">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP133438</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2997740">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2997740</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3021800</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>Human organoid samples: Pools of 5-10 organoids per replicate were harvested in TRIzol at day 28 for RNA extraction. Mouse organoid samples: Three pools of 16 organoids were isolated in TRIzol after 6 days of differentiation for EV and NOTCH2NL-Sh_T197I organoids. RNA was isolated using standard TRIzol protocol, followed by DNaseI treatment (Rochte) and column purification (Zymo RNA clean and concentrator 5). mRNA was isolated from total RNA using polyA selection Dynabeads mRNA DIRECT Micro Purification Kit (Thermofisher). Library was prepared using strand-specific Ion Total RNA-seq Kit v2 (Thermofisher) and Ion Xpress RNA-seq Barcode 1-16 (Thermofisher) to label different samples.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303021800</ID>
          <LABEL>GSM3021800</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3021800</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3021801" accession="SRX3741069">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3741069</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3021801</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3021801: RNA-seq NOTCH2NL KO rep 2; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP133438" refname="GSE111082">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP133438</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2997741">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2997741</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3021801</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>Human organoid samples: Pools of 5-10 organoids per replicate were harvested in TRIzol at day 28 for RNA extraction. Mouse organoid samples: Three pools of 16 organoids were isolated in TRIzol after 6 days of differentiation for EV and NOTCH2NL-Sh_T197I organoids. RNA was isolated using standard TRIzol protocol, followed by DNaseI treatment (Rochte) and column purification (Zymo RNA clean and concentrator 5). mRNA was isolated from total RNA using polyA selection Dynabeads mRNA DIRECT Micro Purification Kit (Thermofisher). Library was prepared using strand-specific Ion Total RNA-seq Kit v2 (Thermofisher) and Ion Xpress RNA-seq Barcode 1-16 (Thermofisher) to label different samples.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303021801</ID>
          <LABEL>GSM3021801</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3021801</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3021802" accession="SRX3741070">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3741070</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3021802</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3021802: RNA-seq NOTCH2NL KO rep 3; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP133438" refname="GSE111082">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP133438</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2997742">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2997742</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3021802</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>Human organoid samples: Pools of 5-10 organoids per replicate were harvested in TRIzol at day 28 for RNA extraction. Mouse organoid samples: Three pools of 16 organoids were isolated in TRIzol after 6 days of differentiation for EV and NOTCH2NL-Sh_T197I organoids. RNA was isolated using standard TRIzol protocol, followed by DNaseI treatment (Rochte) and column purification (Zymo RNA clean and concentrator 5). mRNA was isolated from total RNA using polyA selection Dynabeads mRNA DIRECT Micro Purification Kit (Thermofisher). Library was prepared using strand-specific Ion Total RNA-seq Kit v2 (Thermofisher) and Ion Xpress RNA-seq Barcode 1-16 (Thermofisher) to label different samples.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303021802</ID>
          <LABEL>GSM3021802</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3021802</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3021803" accession="SRX3741071">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3741071</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3021803</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3021803: RNA-seq EV ctrl rep 1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP133438" refname="GSE111082">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP133438</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2997743">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2997743</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3021803</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>Human organoid samples: Pools of 5-10 organoids per replicate were harvested in TRIzol at day 28 for RNA extraction. Mouse organoid samples: Three pools of 16 organoids were isolated in TRIzol after 6 days of differentiation for EV and NOTCH2NL-Sh_T197I organoids. RNA was isolated using standard TRIzol protocol, followed by DNaseI treatment (Rochte) and column purification (Zymo RNA clean and concentrator 5). mRNA was isolated from total RNA using polyA selection Dynabeads mRNA DIRECT Micro Purification Kit (Thermofisher). Library was prepared using strand-specific Ion Total RNA-seq Kit v2 (Thermofisher) and Ion Xpress RNA-seq Barcode 1-16 (Thermofisher) to label different samples.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303021803</ID>
          <LABEL>GSM3021803</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3021803</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3021804" accession="SRX3741072">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3741072</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3021804</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3021804: RNA-seq EV ctrl rep 2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP133438" refname="GSE111082">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP133438</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2997744">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2997744</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3021804</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>Human organoid samples: Pools of 5-10 organoids per replicate were harvested in TRIzol at day 28 for RNA extraction. Mouse organoid samples: Three pools of 16 organoids were isolated in TRIzol after 6 days of differentiation for EV and NOTCH2NL-Sh_T197I organoids. RNA was isolated using standard TRIzol protocol, followed by DNaseI treatment (Rochte) and column purification (Zymo RNA clean and concentrator 5). mRNA was isolated from total RNA using polyA selection Dynabeads mRNA DIRECT Micro Purification Kit (Thermofisher). Library was prepared using strand-specific Ion Total RNA-seq Kit v2 (Thermofisher) and Ion Xpress RNA-seq Barcode 1-16 (Thermofisher) to label different samples.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303021804</ID>
          <LABEL>GSM3021804</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3021804</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3021805" accession="SRX3741073">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3741073</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3021805</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3021805: RNA-seq EV ctrl rep 3; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP133438" refname="GSE111082">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP133438</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2997745">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2997745</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3021805</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>Human organoid samples: Pools of 5-10 organoids per replicate were harvested in TRIzol at day 28 for RNA extraction. Mouse organoid samples: Three pools of 16 organoids were isolated in TRIzol after 6 days of differentiation for EV and NOTCH2NL-Sh_T197I organoids. RNA was isolated using standard TRIzol protocol, followed by DNaseI treatment (Rochte) and column purification (Zymo RNA clean and concentrator 5). mRNA was isolated from total RNA using polyA selection Dynabeads mRNA DIRECT Micro Purification Kit (Thermofisher). Library was prepared using strand-specific Ion Total RNA-seq Kit v2 (Thermofisher) and Ion Xpress RNA-seq Barcode 1-16 (Thermofisher) to label different samples.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303021805</ID>
          <LABEL>GSM3021805</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3021805</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3021806" accession="SRX3741074">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3741074</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3021806</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3021806: RNA-seq N2NL-Sh_T197I rep 1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP133438" refname="GSE111082">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP133438</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2997746">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2997746</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3021806</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>Human organoid samples: Pools of 5-10 organoids per replicate were harvested in TRIzol at day 28 for RNA extraction. Mouse organoid samples: Three pools of 16 organoids were isolated in TRIzol after 6 days of differentiation for EV and NOTCH2NL-Sh_T197I organoids. RNA was isolated using standard TRIzol protocol, followed by DNaseI treatment (Rochte) and column purification (Zymo RNA clean and concentrator 5). mRNA was isolated from total RNA using polyA selection Dynabeads mRNA DIRECT Micro Purification Kit (Thermofisher). Library was prepared using strand-specific Ion Total RNA-seq Kit v2 (Thermofisher) and Ion Xpress RNA-seq Barcode 1-16 (Thermofisher) to label different samples.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303021806</ID>
          <LABEL>GSM3021806</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3021806</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3021807" accession="SRX3741075">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3741075</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3021807</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3021807: RNA-seq N2NL-Sh_T197I rep 2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP133438" refname="GSE111082">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP133438</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2997747">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2997747</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3021807</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>Human organoid samples: Pools of 5-10 organoids per replicate were harvested in TRIzol at day 28 for RNA extraction. Mouse organoid samples: Three pools of 16 organoids were isolated in TRIzol after 6 days of differentiation for EV and NOTCH2NL-Sh_T197I organoids. RNA was isolated using standard TRIzol protocol, followed by DNaseI treatment (Rochte) and column purification (Zymo RNA clean and concentrator 5). mRNA was isolated from total RNA using polyA selection Dynabeads mRNA DIRECT Micro Purification Kit (Thermofisher). Library was prepared using strand-specific Ion Total RNA-seq Kit v2 (Thermofisher) and Ion Xpress RNA-seq Barcode 1-16 (Thermofisher) to label different samples.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303021807</ID>
          <LABEL>GSM3021807</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3021807</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3021808" accession="SRX3741076">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3741076</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3021808</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3021808: RNA-seq N2NL-Sh_T197I rep 3; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP133438" refname="GSE111082">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP133438</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2997748">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2997748</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3021808</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>Human organoid samples: Pools of 5-10 organoids per replicate were harvested in TRIzol at day 28 for RNA extraction. Mouse organoid samples: Three pools of 16 organoids were isolated in TRIzol after 6 days of differentiation for EV and NOTCH2NL-Sh_T197I organoids. RNA was isolated using standard TRIzol protocol, followed by DNaseI treatment (Rochte) and column purification (Zymo RNA clean and concentrator 5). mRNA was isolated from total RNA using polyA selection Dynabeads mRNA DIRECT Micro Purification Kit (Thermofisher). Library was prepared using strand-specific Ion Total RNA-seq Kit v2 (Thermofisher) and Ion Xpress RNA-seq Barcode 1-16 (Thermofisher) to label different samples.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303021808</ID>
          <LABEL>GSM3021808</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3021808</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
</EXPERIMENT_SET>
