<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX10538874" alias="OIR-1-seq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX10538874</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9388840">OIR-1-seq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>scRNA-Seq of mus musculus: adult male eyes</TITLE>
    <STUDY_REF accession="SRP313889">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP313889</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9388840">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>P17 mouse retinal tissue were enzymatically dissociated as described above and 15 l of single-cell suspension at a concentration of ~900,000 cells/ml was loaded into one channel of the ChromiumTM Single Cell B Chip (10X Genomics1000073), aiming for a recovery of 8000-9000 cells. Cell populations were isolated from mouse retinal. Retinas of the eyes of two mice were taken at a time The Chromium Single Cell 3Library &amp; Gel Bead Kit v3 (10X Genomics, 1000075) was used for single-cell barcoding, cDNA synthesis and library preparation, following manufacturers instructions according to the Single Cell 3Reagent Kits User Guide Version 3. Libraries were sequenced on Illumina novaseq 6000 using paired-end 150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS8657951">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS8657951</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|axiedasen">OIR-1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>OIR-1-seq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC SINGLE CELL</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX10538875" alias="OIR-2-seq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX10538875</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9388840">OIR-2-seq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>scRNA-Seq of mus musculus: adult male eyes</TITLE>
    <STUDY_REF accession="SRP313889">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP313889</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9388840">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>P17 mouse retinal tissue were enzymatically dissociated as described above and 15 l of single-cell suspension at a concentration of ~900,000 cells/ml was loaded into one channel of the ChromiumTM Single Cell B Chip (10X Genomics1000073), aiming for a recovery of 8000-9000 cells. Cell populations were isolated from mouse retinal. Retinas of the eyes of two mice were taken at a time The Chromium Single Cell 3Library &amp; Gel Bead Kit v3 (10X Genomics, 1000075) was used for single-cell barcoding, cDNA synthesis and library preparation, following manufacturers instructions according to the Single Cell 3Reagent Kits User Guide Version 3. Libraries were sequenced on Illumina novaseq 6000 using paired-end 150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS8657952">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS8657952</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|axiedasen">OIR-2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>OIR-2-seq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC SINGLE CELL</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX10538876" alias="OIR-3-seq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX10538876</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9388840">OIR-3-seq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>scRNA-Seq of mus musculus: adult male eyes</TITLE>
    <STUDY_REF accession="SRP313889">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP313889</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9388840">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>P17 mouse retinal tissue were enzymatically dissociated as described above and 15 l of single-cell suspension at a concentration of ~900,000 cells/ml was loaded into one channel of the ChromiumTM Single Cell B Chip (10X Genomics1000073), aiming for a recovery of 8000-9000 cells. Cell populations were isolated from mouse retinal. Retinas of the eyes of two mice were taken at a time The Chromium Single Cell 3Library &amp; Gel Bead Kit v3 (10X Genomics, 1000075) was used for single-cell barcoding, cDNA synthesis and library preparation, following manufacturers instructions according to the Single Cell 3Reagent Kits User Guide Version 3. Libraries were sequenced on Illumina novaseq 6000 using paired-end 150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS8657953">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS8657953</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|axiedasen">OIR-3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>OIR-3-seq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC SINGLE CELL</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX10538877" alias="Ctrl-1-seq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX10538877</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9388840">Ctrl-1-seq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>scRNA-Seq of mus musculus: adult male eyes</TITLE>
    <STUDY_REF accession="SRP313889">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP313889</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9388840">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>P17 mouse retinal tissue were enzymatically dissociated as described above and 15 l of single-cell suspension at a concentration of ~900,000 cells/ml was loaded into one channel of the ChromiumTM Single Cell B Chip (10X Genomics1000073), aiming for a recovery of 8000-9000 cells. Cell populations were isolated from mouse retinal. Retinas of the eyes of two mice were taken at a time The Chromium Single Cell 3Library &amp; Gel Bead Kit v3 (10X Genomics, 1000075) was used for single-cell barcoding, cDNA synthesis and library preparation, following manufacturers instructions according to the Single Cell 3Reagent Kits User Guide Version 3. Libraries were sequenced on Illumina novaseq 6000 using paired-end 150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS8657954">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS8657954</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|axiedasen">Ctrl-1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Ctrl-1-seq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC SINGLE CELL</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX10538878" alias="Ctrl-2-seq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX10538878</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9388840">Ctrl-2-seq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>scRNA-Seq of mus musculus: adult male eyes</TITLE>
    <STUDY_REF accession="SRP313889">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP313889</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9388840">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>P17 mouse retinal tissue were enzymatically dissociated as described above and 15 l of single-cell suspension at a concentration of ~900,000 cells/ml was loaded into one channel of the ChromiumTM Single Cell B Chip (10X Genomics1000073), aiming for a recovery of 8000-9000 cells. Cell populations were isolated from mouse retinal. Retinas of the eyes of two mice were taken at a time The Chromium Single Cell 3Library &amp; Gel Bead Kit v3 (10X Genomics, 1000075) was used for single-cell barcoding, cDNA synthesis and library preparation, following manufacturers instructions according to the Single Cell 3Reagent Kits User Guide Version 3. Libraries were sequenced on Illumina novaseq 6000 using paired-end 150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS8657955">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS8657955</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|axiedasen">Ctrl-2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Ctrl-2-seq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC SINGLE CELL</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX10538879" alias="Ctrl-3-seq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX10538879</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9388840">Ctrl-3-seq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>scRNA-Seq of mus musculus: adult male eyes</TITLE>
    <STUDY_REF accession="SRP313889">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP313889</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9388840">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>P17 mouse retinal tissue were enzymatically dissociated as described above and 15 l of single-cell suspension at a concentration of ~900,000 cells/ml was loaded into one channel of the ChromiumTM Single Cell B Chip (10X Genomics1000073), aiming for a recovery of 8000-9000 cells. Cell populations were isolated from mouse retinal. Retinas of the eyes of two mice were taken at a time The Chromium Single Cell 3Library &amp; Gel Bead Kit v3 (10X Genomics, 1000075) was used for single-cell barcoding, cDNA synthesis and library preparation, following manufacturers instructions according to the Single Cell 3Reagent Kits User Guide Version 3. Libraries were sequenced on Illumina novaseq 6000 using paired-end 150 bp.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS8657956">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS8657956</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|axiedasen">Ctrl-3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Ctrl-3-seq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC SINGLE CELL</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
