<?xml version="1.0" encoding="UTF-8"?>
<SAMPLE_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <SAMPLE alias="SAMEA3356196" accession="ERS710488">
    <IDENTIFIERS>
      <PRIMARY_ID>ERS710488</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMEA3356196</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>eNSC Bmi1-2</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>10090</TAXON_ID>
      <SCIENTIFIC_NAME>Mus musculus</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <DESCRIPTION>Protocols: Isolated neural stem cells from E18.5 or adult Swiss Webster mice were grown under non-adherent conditions for three weeks/two passages (eNSCs) or four weeks/three passages (aNSCs) prior to RNA isolation Embryonic NSCs were acutely transduced with empty vector (EV) or Bmi1-overexpressing lentiviral vector; adult NSCs were allowed to recover overnight prior to transduction Total RNA was isolated using RNAeasy Plus Micro kit (Qiagen) 150-250 ng RNA was used for library construction. Ribosomal RNA was removed using the Ribo-Zero Magnetic Kit (Epicentre), and libraries prepared using the ScripSeq V2 RNA-seq Kit (Epicentre), using the low input protocol.</DESCRIPTION>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>ENA-FIRST-PUBLIC</TAG>
        <VALUE>2015-12-01T17:02:04Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>ENA-LAST-UPDATE</TAG>
        <VALUE>2018-03-09T00:37:20Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>External Id</TAG>
        <VALUE>SAMEA3356196</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC center name</TAG>
        <VALUE>Wadsworth Center, NY State Dept of Health</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC first public</TAG>
        <VALUE>2015-12-01T17:02:04Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC last update</TAG>
        <VALUE>2018-03-09T00:37:20Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC status</TAG>
        <VALUE>public</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>Submitter Id</TAG>
        <VALUE>E-MTAB-3491:eNSC Bmi1-2</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>broker name</TAG>
        <VALUE>ArrayExpress</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>cell type</TAG>
        <VALUE>neural stem cell</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>common name</TAG>
        <VALUE>house mouse</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>developmental stage</TAG>
        <VALUE>embryonic day 18.5</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>genetic modification</TAG>
        <VALUE>Bmi1-overexpressing lentiviral vector</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>growth condition</TAG>
        <VALUE>neurospheres</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sample name</TAG>
        <VALUE>E-MTAB-3491:eNSC Bmi1-2</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>scientific_name</TAG>
        <VALUE>Mus musculus</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="SAMEA3356197" accession="ERS710489">
    <IDENTIFIERS>
      <PRIMARY_ID>ERS710489</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMEA3356197</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>aNSC EV-2</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>10090</TAXON_ID>
      <SCIENTIFIC_NAME>Mus musculus</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <DESCRIPTION>Protocols: Isolated neural stem cells from E18.5 or adult Swiss Webster mice were grown under non-adherent conditions for three weeks/two passages (eNSCs) or four weeks/three passages (aNSCs) prior to RNA isolation Embryonic NSCs were acutely transduced with empty vector (EV) or Bmi1-overexpressing lentiviral vector; adult NSCs were allowed to recover overnight prior to transduction Total RNA was isolated using RNAeasy Plus Micro kit (Qiagen) 150-250 ng RNA was used for library construction. Ribosomal RNA was removed using the Ribo-Zero Magnetic Kit (Epicentre), and libraries prepared using the ScripSeq V2 RNA-seq Kit (Epicentre), using the low input protocol.</DESCRIPTION>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>ENA-FIRST-PUBLIC</TAG>
        <VALUE>2015-12-01T17:02:04Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>ENA-LAST-UPDATE</TAG>
        <VALUE>2018-03-09T00:37:20Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>External Id</TAG>
        <VALUE>SAMEA3356197</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC center name</TAG>
        <VALUE>Wadsworth Center, NY State Dept of Health</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC first public</TAG>
        <VALUE>2015-12-01T17:02:04Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC last update</TAG>
        <VALUE>2018-03-09T00:37:20Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC status</TAG>
        <VALUE>public</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>Submitter Id</TAG>
        <VALUE>E-MTAB-3491:aNSC EV-2</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>broker name</TAG>
        <VALUE>ArrayExpress</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>cell type</TAG>
        <VALUE>neural stem cell</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>common name</TAG>
        <VALUE>house mouse</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>developmental stage</TAG>
        <VALUE>adult</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>genetic modification</TAG>
        <VALUE>empty vector control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>growth condition</TAG>
        <VALUE>neurospheres</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sample name</TAG>
        <VALUE>E-MTAB-3491:aNSC EV-2</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>scientific_name</TAG>
        <VALUE>Mus musculus</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="SAMEA3356198" accession="ERS710490">
    <IDENTIFIERS>
      <PRIMARY_ID>ERS710490</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMEA3356198</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>eNSC H1-2</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>10090</TAXON_ID>
      <SCIENTIFIC_NAME>Mus musculus</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <DESCRIPTION>Protocols: Isolated neural stem cells from E18.5 or adult Swiss Webster mice were grown under non-adherent conditions for three weeks/two passages (eNSCs) or four weeks/three passages (aNSCs) prior to RNA isolation Embryonic NSCs were acutely transduced with empty vector (EV) or Bmi1-overexpressing lentiviral vector; adult NSCs were allowed to recover overnight prior to transduction Total RNA was isolated using RNAeasy Plus Micro kit (Qiagen) 150-250 ng RNA was used for library construction. Ribosomal RNA was removed using the Ribo-Zero Magnetic Kit (Epicentre), and libraries prepared using the ScripSeq V2 RNA-seq Kit (Epicentre), using the low input protocol.</DESCRIPTION>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>ENA-FIRST-PUBLIC</TAG>
        <VALUE>2015-12-01T17:02:04Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>ENA-LAST-UPDATE</TAG>
        <VALUE>2018-03-09T00:37:20Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>External Id</TAG>
        <VALUE>SAMEA3356198</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC center name</TAG>
        <VALUE>Wadsworth Center, NY State Dept of Health</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC first public</TAG>
        <VALUE>2015-12-01T17:02:04Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC last update</TAG>
        <VALUE>2018-03-09T00:37:20Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC status</TAG>
        <VALUE>public</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>Submitter Id</TAG>
        <VALUE>E-MTAB-3491:eNSC H1-2</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>broker name</TAG>
        <VALUE>ArrayExpress</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>cell type</TAG>
        <VALUE>neural stem cell</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>common name</TAG>
        <VALUE>house mouse</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>developmental stage</TAG>
        <VALUE>embryonic day 18.5</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>genetic modification</TAG>
        <VALUE>empty vector control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>growth condition</TAG>
        <VALUE>neurospheres</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sample name</TAG>
        <VALUE>E-MTAB-3491:eNSC H1-2</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>scientific_name</TAG>
        <VALUE>Mus musculus</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="SAMEA3356199" accession="ERS710491">
    <IDENTIFIERS>
      <PRIMARY_ID>ERS710491</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMEA3356199</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>aNSC Bmi1-1</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>10090</TAXON_ID>
      <SCIENTIFIC_NAME>Mus musculus</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <DESCRIPTION>Protocols: Isolated neural stem cells from E18.5 or adult Swiss Webster mice were grown under non-adherent conditions for three weeks/two passages (eNSCs) or four weeks/three passages (aNSCs) prior to RNA isolation Embryonic NSCs were acutely transduced with empty vector (EV) or Bmi1-overexpressing lentiviral vector; adult NSCs were allowed to recover overnight prior to transduction Total RNA was isolated using RNAeasy Plus Micro kit (Qiagen) 150-250 ng RNA was used for library construction. Ribosomal RNA was removed using the Ribo-Zero Magnetic Kit (Epicentre), and libraries prepared using the ScripSeq V2 RNA-seq Kit (Epicentre), using the low input protocol.</DESCRIPTION>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>ENA-FIRST-PUBLIC</TAG>
        <VALUE>2015-12-01T17:02:04Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>ENA-LAST-UPDATE</TAG>
        <VALUE>2018-03-09T00:37:20Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>External Id</TAG>
        <VALUE>SAMEA3356199</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC center name</TAG>
        <VALUE>Wadsworth Center, NY State Dept of Health</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC first public</TAG>
        <VALUE>2015-12-01T17:02:04Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC last update</TAG>
        <VALUE>2018-03-09T00:37:20Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC status</TAG>
        <VALUE>public</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>Submitter Id</TAG>
        <VALUE>E-MTAB-3491:aNSC Bmi1-1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>broker name</TAG>
        <VALUE>ArrayExpress</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>cell type</TAG>
        <VALUE>neural stem cell</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>common name</TAG>
        <VALUE>house mouse</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>developmental stage</TAG>
        <VALUE>adult</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>genetic modification</TAG>
        <VALUE>Bmi1-overexpressing lentiviral vector</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>growth condition</TAG>
        <VALUE>neurospheres</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sample name</TAG>
        <VALUE>E-MTAB-3491:aNSC Bmi1-1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>scientific_name</TAG>
        <VALUE>Mus musculus</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="SAMEA3356200" accession="ERS710492">
    <IDENTIFIERS>
      <PRIMARY_ID>ERS710492</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMEA3356200</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>aNSC EV-1</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>10090</TAXON_ID>
      <SCIENTIFIC_NAME>Mus musculus</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <DESCRIPTION>Protocols: Isolated neural stem cells from E18.5 or adult Swiss Webster mice were grown under non-adherent conditions for three weeks/two passages (eNSCs) or four weeks/three passages (aNSCs) prior to RNA isolation Embryonic NSCs were acutely transduced with empty vector (EV) or Bmi1-overexpressing lentiviral vector; adult NSCs were allowed to recover overnight prior to transduction Total RNA was isolated using RNAeasy Plus Micro kit (Qiagen) 150-250 ng RNA was used for library construction. Ribosomal RNA was removed using the Ribo-Zero Magnetic Kit (Epicentre), and libraries prepared using the ScripSeq V2 RNA-seq Kit (Epicentre), using the low input protocol.</DESCRIPTION>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>ENA-FIRST-PUBLIC</TAG>
        <VALUE>2015-12-01T17:02:04Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>ENA-LAST-UPDATE</TAG>
        <VALUE>2018-03-09T00:37:36Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>External Id</TAG>
        <VALUE>SAMEA3356200</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC center name</TAG>
        <VALUE>Wadsworth Center, NY State Dept of Health</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC first public</TAG>
        <VALUE>2015-12-01T17:02:04Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC last update</TAG>
        <VALUE>2018-03-09T00:37:36Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC status</TAG>
        <VALUE>public</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>Submitter Id</TAG>
        <VALUE>E-MTAB-3491:aNSC EV-1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>broker name</TAG>
        <VALUE>ArrayExpress</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>cell type</TAG>
        <VALUE>neural stem cell</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>common name</TAG>
        <VALUE>house mouse</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>developmental stage</TAG>
        <VALUE>adult</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>genetic modification</TAG>
        <VALUE>empty vector control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>growth condition</TAG>
        <VALUE>neurospheres</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sample name</TAG>
        <VALUE>E-MTAB-3491:aNSC EV-1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>scientific_name</TAG>
        <VALUE>Mus musculus</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="SAMEA3356201" accession="ERS710493">
    <IDENTIFIERS>
      <PRIMARY_ID>ERS710493</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMEA3356201</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>aNSC Bmi1-2</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>10090</TAXON_ID>
      <SCIENTIFIC_NAME>Mus musculus</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <DESCRIPTION>Protocols: Isolated neural stem cells from E18.5 or adult Swiss Webster mice were grown under non-adherent conditions for three weeks/two passages (eNSCs) or four weeks/three passages (aNSCs) prior to RNA isolation Embryonic NSCs were acutely transduced with empty vector (EV) or Bmi1-overexpressing lentiviral vector; adult NSCs were allowed to recover overnight prior to transduction Total RNA was isolated using RNAeasy Plus Micro kit (Qiagen) 150-250 ng RNA was used for library construction. Ribosomal RNA was removed using the Ribo-Zero Magnetic Kit (Epicentre), and libraries prepared using the ScripSeq V2 RNA-seq Kit (Epicentre), using the low input protocol.</DESCRIPTION>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>ENA-FIRST-PUBLIC</TAG>
        <VALUE>2015-12-01T17:02:04Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>ENA-LAST-UPDATE</TAG>
        <VALUE>2018-03-09T00:37:36Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>External Id</TAG>
        <VALUE>SAMEA3356201</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC center name</TAG>
        <VALUE>Wadsworth Center, NY State Dept of Health</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC first public</TAG>
        <VALUE>2015-12-01T17:02:04Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC last update</TAG>
        <VALUE>2018-03-09T00:37:36Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC status</TAG>
        <VALUE>public</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>Submitter Id</TAG>
        <VALUE>E-MTAB-3491:aNSC Bmi1-2</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>broker name</TAG>
        <VALUE>ArrayExpress</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>cell type</TAG>
        <VALUE>neural stem cell</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>common name</TAG>
        <VALUE>house mouse</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>developmental stage</TAG>
        <VALUE>adult</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>genetic modification</TAG>
        <VALUE>Bmi1-overexpressing lentiviral vector</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>growth condition</TAG>
        <VALUE>neurospheres</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sample name</TAG>
        <VALUE>E-MTAB-3491:aNSC Bmi1-2</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>scientific_name</TAG>
        <VALUE>Mus musculus</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="SAMEA3356202" accession="ERS710494">
    <IDENTIFIERS>
      <PRIMARY_ID>ERS710494</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMEA3356202</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>eNSC H1-1</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>10090</TAXON_ID>
      <SCIENTIFIC_NAME>Mus musculus</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <DESCRIPTION>Protocols: Isolated neural stem cells from E18.5 or adult Swiss Webster mice were grown under non-adherent conditions for three weeks/two passages (eNSCs) or four weeks/three passages (aNSCs) prior to RNA isolation Embryonic NSCs were acutely transduced with empty vector (EV) or Bmi1-overexpressing lentiviral vector; adult NSCs were allowed to recover overnight prior to transduction Total RNA was isolated using RNAeasy Plus Micro kit (Qiagen) 150-250 ng RNA was used for library construction. Ribosomal RNA was removed using the Ribo-Zero Magnetic Kit (Epicentre), and libraries prepared using the ScripSeq V2 RNA-seq Kit (Epicentre), using the low input protocol.</DESCRIPTION>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>ENA-FIRST-PUBLIC</TAG>
        <VALUE>2015-12-01T17:02:04Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>ENA-LAST-UPDATE</TAG>
        <VALUE>2018-03-09T00:37:36Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>External Id</TAG>
        <VALUE>SAMEA3356202</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC center name</TAG>
        <VALUE>Wadsworth Center, NY State Dept of Health</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC first public</TAG>
        <VALUE>2015-12-01T17:02:04Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC last update</TAG>
        <VALUE>2018-03-09T00:37:36Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC status</TAG>
        <VALUE>public</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>Submitter Id</TAG>
        <VALUE>E-MTAB-3491:eNSC H1-1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>broker name</TAG>
        <VALUE>ArrayExpress</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>cell type</TAG>
        <VALUE>neural stem cell</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>common name</TAG>
        <VALUE>house mouse</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>developmental stage</TAG>
        <VALUE>embryonic day 18.5</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>genetic modification</TAG>
        <VALUE>empty vector control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>growth condition</TAG>
        <VALUE>neurospheres</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sample name</TAG>
        <VALUE>E-MTAB-3491:eNSC H1-1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>scientific_name</TAG>
        <VALUE>Mus musculus</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="SAMEA3356203" accession="ERS710495">
    <IDENTIFIERS>
      <PRIMARY_ID>ERS710495</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMEA3356203</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>eNSC Bmi1-1</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>10090</TAXON_ID>
      <SCIENTIFIC_NAME>Mus musculus</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <DESCRIPTION>Protocols: Isolated neural stem cells from E18.5 or adult Swiss Webster mice were grown under non-adherent conditions for three weeks/two passages (eNSCs) or four weeks/three passages (aNSCs) prior to RNA isolation Embryonic NSCs were acutely transduced with empty vector (EV) or Bmi1-overexpressing lentiviral vector; adult NSCs were allowed to recover overnight prior to transduction Total RNA was isolated using RNAeasy Plus Micro kit (Qiagen) 150-250 ng RNA was used for library construction. Ribosomal RNA was removed using the Ribo-Zero Magnetic Kit (Epicentre), and libraries prepared using the ScripSeq V2 RNA-seq Kit (Epicentre), using the low input protocol.</DESCRIPTION>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>ENA-FIRST-PUBLIC</TAG>
        <VALUE>2015-12-01T17:02:04Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>ENA-LAST-UPDATE</TAG>
        <VALUE>2018-03-09T00:37:36Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>External Id</TAG>
        <VALUE>SAMEA3356203</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC center name</TAG>
        <VALUE>Wadsworth Center, NY State Dept of Health</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC first public</TAG>
        <VALUE>2015-12-01T17:02:04Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC last update</TAG>
        <VALUE>2018-03-09T00:37:36Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC status</TAG>
        <VALUE>public</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>Submitter Id</TAG>
        <VALUE>E-MTAB-3491:eNSC Bmi1-1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>broker name</TAG>
        <VALUE>ArrayExpress</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>cell type</TAG>
        <VALUE>neural stem cell</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>common name</TAG>
        <VALUE>house mouse</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>developmental stage</TAG>
        <VALUE>embryonic day 18.5</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>genetic modification</TAG>
        <VALUE>Bmi1-overexpressing lentiviral vector</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>growth condition</TAG>
        <VALUE>neurospheres</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sample name</TAG>
        <VALUE>E-MTAB-3491:eNSC Bmi1-1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>scientific_name</TAG>
        <VALUE>Mus musculus</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
</SAMPLE_SET>
