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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX23174298" alias="Control 1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23174298</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14140590">Control 1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA seq of cortical mouse astrocytes Control 1</TITLE>
    <STUDY_REF accession="SRP483350">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP483350</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14140590">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA from FACS isolated cells (astrocytes) was extracted with the Purelink RNA Micro kit (ThermoFisher). RNA was amplified with the MessageAmp II aRNA Amplification kit (ThermoFisher), which included a polyA selection.  Libraries from the amplified RNA were prepared using the Illumina Stranded mRNA kit (omitting the polyA tail pull down step). All samples were then multiplexed.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20123594">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20123594</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|jill.stobart@orcid">Control-119512</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Control 1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23174299" alias="Control 2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23174299</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14140590">Control 2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNAseqofcorticalmouseastrocytesControl 2</TITLE>
    <STUDY_REF accession="SRP483350">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP483350</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14140590">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA from FACS isolated cells (astrocytes) was extracted with the Purelink RNA Micro kit (ThermoFisher). RNA was amplified with the MessageAmp II aRNA Amplification kit (ThermoFisher), which included a polyA selection.  Libraries from the amplified RNA were prepared using the Illumina Stranded mRNA kit (omitting the polyA tail pull down step). All samples were then multiplexed.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20123595">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20123595</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|jill.stobart@orcid">Control-119513</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Control 2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23174300" alias="Grin1KD 2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23174300</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14140590">Grin1KD 2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA seq of cortical mouse astrocytes Grin1KD 2</TITLE>
    <STUDY_REF accession="SRP483350">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP483350</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14140590">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA from FACS isolated cells (astrocytes) was extracted with the Purelink RNA Micro kit (ThermoFisher). RNA was amplified with the MessageAmp II aRNA Amplification kit (ThermoFisher), which included a polyA selection.  Libraries from the amplified RNA were prepared using the Illumina Stranded mRNA kit (omitting the polyA tail pull down step). All samples were then multiplexed.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20123596">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20123596</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|jill.stobart@orcid">Grin1KD-119515</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Grin1KD 2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23174301" alias="Grin1KD 3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23174301</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14140590">Grin1KD 3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNAseqofcorticalmouseastrocytesGrin1KD 3</TITLE>
    <STUDY_REF accession="SRP483350">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP483350</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14140590">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA from FACS isolated cells (astrocytes) was extracted with the Purelink RNA Micro kit (ThermoFisher). RNA was amplified with the MessageAmp II aRNA Amplification kit (ThermoFisher), which included a polyA selection.  Libraries from the amplified RNA were prepared using the Illumina Stranded mRNA kit (omitting the polyA tail pull down step). All samples were then multiplexed.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20123598">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20123598</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|jill.stobart@orcid">Grin1KD-119516</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Grin1KD 3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23174302" alias="Grin1KD 4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23174302</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14140590">Grin1KD 4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNAseqofcorticalmouseastrocytesGrin1KD 4</TITLE>
    <STUDY_REF accession="SRP483350">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP483350</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14140590">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA from FACS isolated cells (astrocytes) was extracted with the Purelink RNA Micro kit (ThermoFisher). RNA was amplified with the MessageAmp II aRNA Amplification kit (ThermoFisher), which included a polyA selection.  Libraries from the amplified RNA were prepared using the Illumina Stranded mRNA kit (omitting the polyA tail pull down step). All samples were then multiplexed.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20123597">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20123597</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|jill.stobart@orcid">Grin1KD-149742</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Grin1KD 4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23174303" alias="Grin1KD 5">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23174303</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14140590">Grin1KD 5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNAseqofcorticalmouseastrocytesGrin1KD 5</TITLE>
    <STUDY_REF accession="SRP483350">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP483350</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14140590">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA from FACS isolated cells (astrocytes) was extracted with the Purelink RNA Micro kit (ThermoFisher). RNA was amplified with the MessageAmp II aRNA Amplification kit (ThermoFisher), which included a polyA selection.  Libraries from the amplified RNA were prepared using the Illumina Stranded mRNA kit (omitting the polyA tail pull down step). All samples were then multiplexed.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20123599">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20123599</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|jill.stobart@orcid">Grin1KD-153307</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Grin1KD 5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23174304" alias="Grin1KD 6">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23174304</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14140590">Grin1KD 6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNAseqofcorticalmouseastrocytesGrin1KD 6</TITLE>
    <STUDY_REF accession="SRP483350">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP483350</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14140590">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA from FACS isolated cells (astrocytes) was extracted with the Purelink RNA Micro kit (ThermoFisher). RNA was amplified with the MessageAmp II aRNA Amplification kit (ThermoFisher), which included a polyA selection.  Libraries from the amplified RNA were prepared using the Illumina Stranded mRNA kit (omitting the polyA tail pull down step). All samples were then multiplexed.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20123600">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20123600</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|jill.stobart@orcid">Grin1KD-153308</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Grin1KD 6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23174305" alias="Grin1KD 7">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23174305</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14140590">Grin1KD 7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNAseqofcorticalmouseastrocytesGrin1KD 7</TITLE>
    <STUDY_REF accession="SRP483350">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP483350</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14140590">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA from FACS isolated cells (astrocytes) was extracted with the Purelink RNA Micro kit (ThermoFisher). RNA was amplified with the MessageAmp II aRNA Amplification kit (ThermoFisher), which included a polyA selection.  Libraries from the amplified RNA were prepared using the Illumina Stranded mRNA kit (omitting the polyA tail pull down step). All samples were then multiplexed.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20123601">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20123601</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|jill.stobart@orcid">Grin1KD-153316</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Grin1KD 7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23174306" alias="Control 3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23174306</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14140590">Control 3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNAseqofcorticalmouseastrocytesControl 3</TITLE>
    <STUDY_REF accession="SRP483350">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP483350</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14140590">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA from FACS isolated cells (astrocytes) was extracted with the Purelink RNA Micro kit (ThermoFisher). RNA was amplified with the MessageAmp II aRNA Amplification kit (ThermoFisher), which included a polyA selection.  Libraries from the amplified RNA were prepared using the Illumina Stranded mRNA kit (omitting the polyA tail pull down step). All samples were then multiplexed.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20123602">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20123602</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|jill.stobart@orcid">Control-149739</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Control 3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23174307" alias="Control 4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23174307</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14140590">Control 4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNAseqofcorticalmouseastrocytesControl 4</TITLE>
    <STUDY_REF accession="SRP483350">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP483350</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14140590">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA from FACS isolated cells (astrocytes) was extracted with the Purelink RNA Micro kit (ThermoFisher). RNA was amplified with the MessageAmp II aRNA Amplification kit (ThermoFisher), which included a polyA selection.  Libraries from the amplified RNA were prepared using the Illumina Stranded mRNA kit (omitting the polyA tail pull down step). All samples were then multiplexed.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20123603">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20123603</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|jill.stobart@orcid">Control-149740</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Control 4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23174308" alias="Control 5">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23174308</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14140590">Control 5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNAseqofcorticalmouseastrocytesControl 5</TITLE>
    <STUDY_REF accession="SRP483350">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP483350</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14140590">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA from FACS isolated cells (astrocytes) was extracted with the Purelink RNA Micro kit (ThermoFisher). RNA was amplified with the MessageAmp II aRNA Amplification kit (ThermoFisher), which included a polyA selection.  Libraries from the amplified RNA were prepared using the Illumina Stranded mRNA kit (omitting the polyA tail pull down step). All samples were then multiplexed.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20123604">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20123604</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|jill.stobart@orcid">Control-149741</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Control 5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23174309" alias="Control 6">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23174309</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14140590">Control 6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNAseqofcorticalmouseastrocytesControl 6</TITLE>
    <STUDY_REF accession="SRP483350">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP483350</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14140590">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA from FACS isolated cells (astrocytes) was extracted with the Purelink RNA Micro kit (ThermoFisher). RNA was amplified with the MessageAmp II aRNA Amplification kit (ThermoFisher), which included a polyA selection.  Libraries from the amplified RNA were prepared using the Illumina Stranded mRNA kit (omitting the polyA tail pull down step). All samples were then multiplexed.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20123605">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20123605</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|jill.stobart@orcid">Control-153309</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Control 6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23174310" alias="Control 7">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23174310</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14140590">Control 7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNAseqofcorticalmouseastrocytesControl 7</TITLE>
    <STUDY_REF accession="SRP483350">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP483350</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14140590">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA from FACS isolated cells (astrocytes) was extracted with the Purelink RNA Micro kit (ThermoFisher). RNA was amplified with the MessageAmp II aRNA Amplification kit (ThermoFisher), which included a polyA selection.  Libraries from the amplified RNA were prepared using the Illumina Stranded mRNA kit (omitting the polyA tail pull down step). All samples were then multiplexed.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20123606">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20123606</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|jill.stobart@orcid">Control-153310</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Control 7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23174311" alias="Control 8">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23174311</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14140590">Control 8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNAseqofcorticalmouseastrocytesControl 8</TITLE>
    <STUDY_REF accession="SRP483350">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP483350</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14140590">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA from FACS isolated cells (astrocytes) was extracted with the Purelink RNA Micro kit (ThermoFisher). RNA was amplified with the MessageAmp II aRNA Amplification kit (ThermoFisher), which included a polyA selection.  Libraries from the amplified RNA were prepared using the Illumina Stranded mRNA kit (omitting the polyA tail pull down step). All samples were then multiplexed.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20123607">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20123607</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|jill.stobart@orcid">Control-153312</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Control 8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23174312" alias="Control 9">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23174312</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14140590">Control 9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNAseqofcorticalmouseastrocytesControl 9</TITLE>
    <STUDY_REF accession="SRP483350">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP483350</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14140590">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA from FACS isolated cells (astrocytes) was extracted with the Purelink RNA Micro kit (ThermoFisher). RNA was amplified with the MessageAmp II aRNA Amplification kit (ThermoFisher), which included a polyA selection.  Libraries from the amplified RNA were prepared using the Illumina Stranded mRNA kit (omitting the polyA tail pull down step). All samples were then multiplexed.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20123609">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20123609</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|jill.stobart@orcid">Control-153313</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Control 9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX23174313" alias="Grin1KD 1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23174313</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14140590">Grin1KD 1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA seq of cortical mouse astrocytes Grin1KD 1</TITLE>
    <STUDY_REF accession="SRP483350">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP483350</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14140590">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA from FACS isolated cells (astrocytes) was extracted with the Purelink RNA Micro kit (ThermoFisher). RNA was amplified with the MessageAmp II aRNA Amplification kit (ThermoFisher), which included a polyA selection.  Libraries from the amplified RNA were prepared using the Illumina Stranded mRNA kit (omitting the polyA tail pull down step). All samples were then multiplexed.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20123608">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20123608</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|jill.stobart@orcid">Grin1KD-119514</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Grin1KD 1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
