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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX18311923" alias="GSM6742797_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18311923</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6742797_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6742797: A2776; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408651">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408651</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903193</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15801945">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15801945</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6742797</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6742797</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC SINGLE CELL</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Mice were perfused with cold PBS, and half of each brain tissue, excluding olfactory and cerebellum, were immediately dissected and dissociated using Neural Tissue Dissociation Kit (P) (Miltenyi). Myelin was removed after tissue dissociation using Myelin Removal Beads II (Miltenyi). Dead Cell Removal Kit (Miltenyi, USA) was applied to dead cells and debris. Libraries were prepared using the Chromium Next GEM Single Cell 3' Kit v3.1 and Chip G Single Cell Kit (10x Genomics, USA) according to manufacturer's protocol.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18311924" alias="GSM6742798_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18311924</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6742798_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6742798: A2779; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408651">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408651</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903193</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
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      <SAMPLE_DESCRIPTOR accession="SRS15801947">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15801947</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6742798</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6742798</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC SINGLE CELL</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Mice were perfused with cold PBS, and half of each brain tissue, excluding olfactory and cerebellum, were immediately dissected and dissociated using Neural Tissue Dissociation Kit (P) (Miltenyi). Myelin was removed after tissue dissociation using Myelin Removal Beads II (Miltenyi). Dead Cell Removal Kit (Miltenyi, USA) was applied to dead cells and debris. Libraries were prepared using the Chromium Next GEM Single Cell 3' Kit v3.1 and Chip G Single Cell Kit (10x Genomics, USA) according to manufacturer's protocol.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18311925" alias="GSM6742799_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18311925</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6742799_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6742799: A2804; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408651">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408651</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903193</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15801946">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15801946</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6742799</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6742799</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC SINGLE CELL</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Mice were perfused with cold PBS, and half of each brain tissue, excluding olfactory and cerebellum, were immediately dissected and dissociated using Neural Tissue Dissociation Kit (P) (Miltenyi). Myelin was removed after tissue dissociation using Myelin Removal Beads II (Miltenyi). Dead Cell Removal Kit (Miltenyi, USA) was applied to dead cells and debris. Libraries were prepared using the Chromium Next GEM Single Cell 3' Kit v3.1 and Chip G Single Cell Kit (10x Genomics, USA) according to manufacturer's protocol.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18311926" alias="GSM6742800_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18311926</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6742800_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6742800: A2814; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408651">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408651</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903193</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15801948">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15801948</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6742800</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6742800</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC SINGLE CELL</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Mice were perfused with cold PBS, and half of each brain tissue, excluding olfactory and cerebellum, were immediately dissected and dissociated using Neural Tissue Dissociation Kit (P) (Miltenyi). Myelin was removed after tissue dissociation using Myelin Removal Beads II (Miltenyi). Dead Cell Removal Kit (Miltenyi, USA) was applied to dead cells and debris. Libraries were prepared using the Chromium Next GEM Single Cell 3' Kit v3.1 and Chip G Single Cell Kit (10x Genomics, USA) according to manufacturer's protocol.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18311927" alias="GSM6742801_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18311927</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6742801_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6742801: A2780; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408651">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408651</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903193</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15801949">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15801949</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6742801</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6742801</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC SINGLE CELL</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Mice were perfused with cold PBS, and half of each brain tissue, excluding olfactory and cerebellum, were immediately dissected and dissociated using Neural Tissue Dissociation Kit (P) (Miltenyi). Myelin was removed after tissue dissociation using Myelin Removal Beads II (Miltenyi). Dead Cell Removal Kit (Miltenyi, USA) was applied to dead cells and debris. Libraries were prepared using the Chromium Next GEM Single Cell 3' Kit v3.1 and Chip G Single Cell Kit (10x Genomics, USA) according to manufacturer's protocol.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18311928" alias="GSM6742802_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18311928</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6742802_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6742802: A2783; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408651">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408651</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903193</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15801950">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15801950</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6742802</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6742802</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC SINGLE CELL</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Mice were perfused with cold PBS, and half of each brain tissue, excluding olfactory and cerebellum, were immediately dissected and dissociated using Neural Tissue Dissociation Kit (P) (Miltenyi). Myelin was removed after tissue dissociation using Myelin Removal Beads II (Miltenyi). Dead Cell Removal Kit (Miltenyi, USA) was applied to dead cells and debris. Libraries were prepared using the Chromium Next GEM Single Cell 3' Kit v3.1 and Chip G Single Cell Kit (10x Genomics, USA) according to manufacturer's protocol.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18311929" alias="GSM6742803_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18311929</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6742803_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6742803: A2806; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408651">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408651</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903193</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15801951">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15801951</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6742803</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6742803</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC SINGLE CELL</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Mice were perfused with cold PBS, and half of each brain tissue, excluding olfactory and cerebellum, were immediately dissected and dissociated using Neural Tissue Dissociation Kit (P) (Miltenyi). Myelin was removed after tissue dissociation using Myelin Removal Beads II (Miltenyi). Dead Cell Removal Kit (Miltenyi, USA) was applied to dead cells and debris. Libraries were prepared using the Chromium Next GEM Single Cell 3' Kit v3.1 and Chip G Single Cell Kit (10x Genomics, USA) according to manufacturer's protocol.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
