<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX22443472" alias="GSM7887113_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22443472</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7887113_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7887113: RRBS Retinal ganglion cells, GFP overexpression, uninjured, replicate 1; Mus musculus; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP470947">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP470947</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1037107</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS19461191">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19461191</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7887113</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7887113</LIBRARY_NAME>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Reduced Representation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>DNA was extracted from retinal ganglion cells using the Quick-DNA Microprep Plus Kit (Zymo Research D4074) following the manufacture's manual. RRBS library preparation and sequencing were done by Zymo Research. Briefly, 10 ng genomic DNA was digested with 30 units of MspI. Fragments were ligated to pre-annealed adapters containing 5'-methyl-cytosine instead of cytosine according to Illumina's specified guidelines. Adaptor-ligated fragments ≥ 50 bp in size were recovered using the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003). The fragments were then bisulfite-treated using the EZ DNA Methylation-Lightning Kit (Zymo Research D5030). Preparative-scale PCR was performed, and the product was purified with the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22443473" alias="GSM7887114_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22443473</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7887114_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7887114: RRBS Retinal ganglion cells, GFP overexpression, uninjured, replicate 2; Mus musculus; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP470947">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP470947</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1037107</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS19461190">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19461190</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7887114</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7887114</LIBRARY_NAME>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Reduced Representation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>DNA was extracted from retinal ganglion cells using the Quick-DNA Microprep Plus Kit (Zymo Research D4074) following the manufacture's manual. RRBS library preparation and sequencing were done by Zymo Research. Briefly, 10 ng genomic DNA was digested with 30 units of MspI. Fragments were ligated to pre-annealed adapters containing 5'-methyl-cytosine instead of cytosine according to Illumina's specified guidelines. Adaptor-ligated fragments ≥ 50 bp in size were recovered using the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003). The fragments were then bisulfite-treated using the EZ DNA Methylation-Lightning Kit (Zymo Research D5030). Preparative-scale PCR was performed, and the product was purified with the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22443474" alias="GSM7887115_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22443474</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7887115_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7887115: RRBS Retinal ganglion cells, GFP overexpression, uninjured, replicate 3; Mus musculus; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP470947">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP470947</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1037107</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS19461193">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19461193</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7887115</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7887115</LIBRARY_NAME>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Reduced Representation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>DNA was extracted from retinal ganglion cells using the Quick-DNA Microprep Plus Kit (Zymo Research D4074) following the manufacture's manual. RRBS library preparation and sequencing were done by Zymo Research. Briefly, 10 ng genomic DNA was digested with 30 units of MspI. Fragments were ligated to pre-annealed adapters containing 5'-methyl-cytosine instead of cytosine according to Illumina's specified guidelines. Adaptor-ligated fragments ≥ 50 bp in size were recovered using the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003). The fragments were then bisulfite-treated using the EZ DNA Methylation-Lightning Kit (Zymo Research D5030). Preparative-scale PCR was performed, and the product was purified with the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22443475" alias="GSM7887116_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22443475</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7887116_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7887116: RRBS Retinal ganglion cells, Ezh2 overexpression, uninjured, replicate 1; Mus musculus; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP470947">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP470947</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1037107</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS19461192">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19461192</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7887116</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7887116</LIBRARY_NAME>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Reduced Representation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>DNA was extracted from retinal ganglion cells using the Quick-DNA Microprep Plus Kit (Zymo Research D4074) following the manufacture's manual. RRBS library preparation and sequencing were done by Zymo Research. Briefly, 10 ng genomic DNA was digested with 30 units of MspI. Fragments were ligated to pre-annealed adapters containing 5'-methyl-cytosine instead of cytosine according to Illumina's specified guidelines. Adaptor-ligated fragments ≥ 50 bp in size were recovered using the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003). The fragments were then bisulfite-treated using the EZ DNA Methylation-Lightning Kit (Zymo Research D5030). Preparative-scale PCR was performed, and the product was purified with the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22443476" alias="GSM7887117_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22443476</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7887117_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7887117: RRBS Retinal ganglion cells, Ezh2 overexpression, uninjured, replicate 2; Mus musculus; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP470947">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP470947</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1037107</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS19461195">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19461195</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7887117</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7887117</LIBRARY_NAME>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Reduced Representation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>DNA was extracted from retinal ganglion cells using the Quick-DNA Microprep Plus Kit (Zymo Research D4074) following the manufacture's manual. RRBS library preparation and sequencing were done by Zymo Research. Briefly, 10 ng genomic DNA was digested with 30 units of MspI. Fragments were ligated to pre-annealed adapters containing 5'-methyl-cytosine instead of cytosine according to Illumina's specified guidelines. Adaptor-ligated fragments ≥ 50 bp in size were recovered using the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003). The fragments were then bisulfite-treated using the EZ DNA Methylation-Lightning Kit (Zymo Research D5030). Preparative-scale PCR was performed, and the product was purified with the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22443477" alias="GSM7887118_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22443477</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7887118_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7887118: RRBS Retinal ganglion cells, Ezh2 overexpression, uninjured, replicate 3; Mus musculus; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP470947">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP470947</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1037107</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS19461194">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19461194</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7887118</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7887118</LIBRARY_NAME>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Reduced Representation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>DNA was extracted from retinal ganglion cells using the Quick-DNA Microprep Plus Kit (Zymo Research D4074) following the manufacture's manual. RRBS library preparation and sequencing were done by Zymo Research. Briefly, 10 ng genomic DNA was digested with 30 units of MspI. Fragments were ligated to pre-annealed adapters containing 5'-methyl-cytosine instead of cytosine according to Illumina's specified guidelines. Adaptor-ligated fragments ≥ 50 bp in size were recovered using the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003). The fragments were then bisulfite-treated using the EZ DNA Methylation-Lightning Kit (Zymo Research D5030). Preparative-scale PCR was performed, and the product was purified with the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22443478" alias="GSM7887119_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22443478</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7887119_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7887119: RRBS Retinal ganglion cells, Ezh2-Y726D overexpression, uninjured, replicate 1; Mus musculus; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP470947">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP470947</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1037107</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS19461196">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19461196</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7887119</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7887119</LIBRARY_NAME>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Reduced Representation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>DNA was extracted from retinal ganglion cells using the Quick-DNA Microprep Plus Kit (Zymo Research D4074) following the manufacture's manual. RRBS library preparation and sequencing were done by Zymo Research. Briefly, 10 ng genomic DNA was digested with 30 units of MspI. Fragments were ligated to pre-annealed adapters containing 5'-methyl-cytosine instead of cytosine according to Illumina's specified guidelines. Adaptor-ligated fragments ≥ 50 bp in size were recovered using the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003). The fragments were then bisulfite-treated using the EZ DNA Methylation-Lightning Kit (Zymo Research D5030). Preparative-scale PCR was performed, and the product was purified with the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22443479" alias="GSM7887120_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22443479</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7887120_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7887120: RRBS Retinal ganglion cells, Ezh2-Y726D overexpression, uninjured, replicate 2; Mus musculus; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP470947">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP470947</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1037107</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS19461197">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19461197</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7887120</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7887120</LIBRARY_NAME>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Reduced Representation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>DNA was extracted from retinal ganglion cells using the Quick-DNA Microprep Plus Kit (Zymo Research D4074) following the manufacture's manual. RRBS library preparation and sequencing were done by Zymo Research. Briefly, 10 ng genomic DNA was digested with 30 units of MspI. Fragments were ligated to pre-annealed adapters containing 5'-methyl-cytosine instead of cytosine according to Illumina's specified guidelines. Adaptor-ligated fragments ≥ 50 bp in size were recovered using the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003). The fragments were then bisulfite-treated using the EZ DNA Methylation-Lightning Kit (Zymo Research D5030). Preparative-scale PCR was performed, and the product was purified with the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22443480" alias="GSM7887121_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22443480</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7887121_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7887121: RRBS Retinal ganglion cells, Ezh2-Y726D overexpression, uninjured, replicate 3; Mus musculus; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP470947">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP470947</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1037107</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS19461198">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19461198</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7887121</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7887121</LIBRARY_NAME>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Reduced Representation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>DNA was extracted from retinal ganglion cells using the Quick-DNA Microprep Plus Kit (Zymo Research D4074) following the manufacture's manual. RRBS library preparation and sequencing were done by Zymo Research. Briefly, 10 ng genomic DNA was digested with 30 units of MspI. Fragments were ligated to pre-annealed adapters containing 5'-methyl-cytosine instead of cytosine according to Illumina's specified guidelines. Adaptor-ligated fragments ≥ 50 bp in size were recovered using the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003). The fragments were then bisulfite-treated using the EZ DNA Methylation-Lightning Kit (Zymo Research D5030). Preparative-scale PCR was performed, and the product was purified with the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22443481" alias="GSM7887122_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22443481</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7887122_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7887122: RRBS Retinal ganglion cells, GFP overexpression, injured, replicate 1; Mus musculus; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP470947">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP470947</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1037107</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS19461199">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19461199</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7887122</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7887122</LIBRARY_NAME>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Reduced Representation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>DNA was extracted from retinal ganglion cells using the Quick-DNA Microprep Plus Kit (Zymo Research D4074) following the manufacture's manual. RRBS library preparation and sequencing were done by Zymo Research. Briefly, 10 ng genomic DNA was digested with 30 units of MspI. Fragments were ligated to pre-annealed adapters containing 5'-methyl-cytosine instead of cytosine according to Illumina's specified guidelines. Adaptor-ligated fragments ≥ 50 bp in size were recovered using the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003). The fragments were then bisulfite-treated using the EZ DNA Methylation-Lightning Kit (Zymo Research D5030). Preparative-scale PCR was performed, and the product was purified with the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22443482" alias="GSM7887123_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22443482</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7887123_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7887123: RRBS Retinal ganglion cells, GFP overexpression, injured, replicate 2; Mus musculus; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP470947">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP470947</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1037107</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS19461200">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19461200</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7887123</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7887123</LIBRARY_NAME>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Reduced Representation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>DNA was extracted from retinal ganglion cells using the Quick-DNA Microprep Plus Kit (Zymo Research D4074) following the manufacture's manual. RRBS library preparation and sequencing were done by Zymo Research. Briefly, 10 ng genomic DNA was digested with 30 units of MspI. Fragments were ligated to pre-annealed adapters containing 5'-methyl-cytosine instead of cytosine according to Illumina's specified guidelines. Adaptor-ligated fragments ≥ 50 bp in size were recovered using the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003). The fragments were then bisulfite-treated using the EZ DNA Methylation-Lightning Kit (Zymo Research D5030). Preparative-scale PCR was performed, and the product was purified with the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22443483" alias="GSM7887124_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22443483</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7887124_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7887124: RRBS Retinal ganglion cells, GFP overexpression, injured, replicate 3; Mus musculus; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP470947">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP470947</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1037107</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS19461201">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19461201</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7887124</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7887124</LIBRARY_NAME>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Reduced Representation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>DNA was extracted from retinal ganglion cells using the Quick-DNA Microprep Plus Kit (Zymo Research D4074) following the manufacture's manual. RRBS library preparation and sequencing were done by Zymo Research. Briefly, 10 ng genomic DNA was digested with 30 units of MspI. Fragments were ligated to pre-annealed adapters containing 5'-methyl-cytosine instead of cytosine according to Illumina's specified guidelines. Adaptor-ligated fragments ≥ 50 bp in size were recovered using the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003). The fragments were then bisulfite-treated using the EZ DNA Methylation-Lightning Kit (Zymo Research D5030). Preparative-scale PCR was performed, and the product was purified with the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22443484" alias="GSM7887125_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22443484</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7887125_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7887125: RRBS Retinal ganglion cells, Ezh2 overexpression, injured, replicate 1; Mus musculus; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP470947">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP470947</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1037107</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS19461202">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19461202</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7887125</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7887125</LIBRARY_NAME>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Reduced Representation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>DNA was extracted from retinal ganglion cells using the Quick-DNA Microprep Plus Kit (Zymo Research D4074) following the manufacture's manual. RRBS library preparation and sequencing were done by Zymo Research. Briefly, 10 ng genomic DNA was digested with 30 units of MspI. Fragments were ligated to pre-annealed adapters containing 5'-methyl-cytosine instead of cytosine according to Illumina's specified guidelines. Adaptor-ligated fragments ≥ 50 bp in size were recovered using the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003). The fragments were then bisulfite-treated using the EZ DNA Methylation-Lightning Kit (Zymo Research D5030). Preparative-scale PCR was performed, and the product was purified with the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22443485" alias="GSM7887126_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22443485</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7887126_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7887126: RRBS Retinal ganglion cells, Ezh2 overexpression, injured, replicate 2; Mus musculus; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP470947">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP470947</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1037107</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS19461203">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19461203</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7887126</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7887126</LIBRARY_NAME>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Reduced Representation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>DNA was extracted from retinal ganglion cells using the Quick-DNA Microprep Plus Kit (Zymo Research D4074) following the manufacture's manual. RRBS library preparation and sequencing were done by Zymo Research. Briefly, 10 ng genomic DNA was digested with 30 units of MspI. Fragments were ligated to pre-annealed adapters containing 5'-methyl-cytosine instead of cytosine according to Illumina's specified guidelines. Adaptor-ligated fragments ≥ 50 bp in size were recovered using the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003). The fragments were then bisulfite-treated using the EZ DNA Methylation-Lightning Kit (Zymo Research D5030). Preparative-scale PCR was performed, and the product was purified with the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22443486" alias="GSM7887127_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22443486</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7887127_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7887127: RRBS Retinal ganglion cells, Ezh2 overexpression, injured, replicate 3; Mus musculus; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP470947">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP470947</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1037107</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS19461205">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19461205</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7887127</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7887127</LIBRARY_NAME>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Reduced Representation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>DNA was extracted from retinal ganglion cells using the Quick-DNA Microprep Plus Kit (Zymo Research D4074) following the manufacture's manual. RRBS library preparation and sequencing were done by Zymo Research. Briefly, 10 ng genomic DNA was digested with 30 units of MspI. Fragments were ligated to pre-annealed adapters containing 5'-methyl-cytosine instead of cytosine according to Illumina's specified guidelines. Adaptor-ligated fragments ≥ 50 bp in size were recovered using the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003). The fragments were then bisulfite-treated using the EZ DNA Methylation-Lightning Kit (Zymo Research D5030). Preparative-scale PCR was performed, and the product was purified with the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22443487" alias="GSM7887128_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22443487</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7887128_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7887128: RRBS Retinal ganglion cells, Ezh2-Y726D overexpression, injured, replicate 1; Mus musculus; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP470947">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP470947</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1037107</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS19461204">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19461204</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7887128</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7887128</LIBRARY_NAME>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Reduced Representation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>DNA was extracted from retinal ganglion cells using the Quick-DNA Microprep Plus Kit (Zymo Research D4074) following the manufacture's manual. RRBS library preparation and sequencing were done by Zymo Research. Briefly, 10 ng genomic DNA was digested with 30 units of MspI. Fragments were ligated to pre-annealed adapters containing 5'-methyl-cytosine instead of cytosine according to Illumina's specified guidelines. Adaptor-ligated fragments ≥ 50 bp in size were recovered using the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003). The fragments were then bisulfite-treated using the EZ DNA Methylation-Lightning Kit (Zymo Research D5030). Preparative-scale PCR was performed, and the product was purified with the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22443488" alias="GSM7887129_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22443488</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7887129_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7887129: RRBS Retinal ganglion cells, Ezh2-Y726D overexpression, injured, replicate 2; Mus musculus; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP470947">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP470947</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1037107</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS19461206">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19461206</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7887129</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7887129</LIBRARY_NAME>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Reduced Representation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>DNA was extracted from retinal ganglion cells using the Quick-DNA Microprep Plus Kit (Zymo Research D4074) following the manufacture's manual. RRBS library preparation and sequencing were done by Zymo Research. Briefly, 10 ng genomic DNA was digested with 30 units of MspI. Fragments were ligated to pre-annealed adapters containing 5'-methyl-cytosine instead of cytosine according to Illumina's specified guidelines. Adaptor-ligated fragments ≥ 50 bp in size were recovered using the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003). The fragments were then bisulfite-treated using the EZ DNA Methylation-Lightning Kit (Zymo Research D5030). Preparative-scale PCR was performed, and the product was purified with the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22443489" alias="GSM7887130_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22443489</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7887130_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7887130: RRBS Retinal ganglion cells, Ezh2-Y726D overexpression, injured, replicate 3; Mus musculus; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP470947">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP470947</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1037107</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS19461207">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19461207</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7887130</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7887130</LIBRARY_NAME>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Reduced Representation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>DNA was extracted from retinal ganglion cells using the Quick-DNA Microprep Plus Kit (Zymo Research D4074) following the manufacture's manual. RRBS library preparation and sequencing were done by Zymo Research. Briefly, 10 ng genomic DNA was digested with 30 units of MspI. Fragments were ligated to pre-annealed adapters containing 5'-methyl-cytosine instead of cytosine according to Illumina's specified guidelines. Adaptor-ligated fragments ≥ 50 bp in size were recovered using the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003). The fragments were then bisulfite-treated using the EZ DNA Methylation-Lightning Kit (Zymo Research D5030). Preparative-scale PCR was performed, and the product was purified with the DNA Clean &amp; Concentrator-5 Kit (Zymo Research D4003).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
