<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX22246011" alias="GSM7868273_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22246011</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7868273_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7868273: LM_snRNA_seq; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP468763">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468763</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1032867</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS19299752">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19299752</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7868273</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7868273</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>FFPE samples were preprocessed on a prototype Singulator™ system. The sample was automatically processed in a NIC+™ cartridge (S2 Genomics #100-215-389) by three 10 min deparaffinization steps (CitriSolv, VWR), rehydrated by successive 1 mL washes of 100%, 100%, 70%, 50%, and 30% ethanol, followed by 2 washes of PBS. The sample was then spun at 1,000g for 3 min and resuspended in 0.5 mL Nuclei Isolation Reagent (NIR, S2 Genomics, #100-063-396) with 0.1 u/mL RNase inhibitor (Protector™, Millipore Sigma, #3335399001); all subsequent solutions had RNase inhibitor. The sample was dissociated to single nuclei in a second NIC+ cartridge with 2 mL of NIR for 10 min followed by a 2 mL wash with Nuclei Storage Reagent (NSR, S2 Genomics, #100-063-405). The single nuclei suspension was spun 500g for 5 min, resuspended in NSR, and counted. Single-nuclei RNA-Seq of FFPE-isolated nuclei suspensions was performed on Chromium instrument (10X genomics) following the user guide manual for Chromium Fixed RNA Kit, Mouse Transcriptome (SinglePlex) Illumina NovaSeq S4 platform (R1 – 28 cycles, i7 – 8 cycles, R2 – 90 cycles)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
