<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX20355854" alias="GSM7350645_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX20355854</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7350645_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7350645: Kidney, rabrhabdomyolysis + vehicle; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP437774">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP437774</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA972752</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17673248">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17673248</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7350645</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7350645</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>The single cell suspension with 95% viability was run on a 10x Chromium Single Cell instrument (10x Genomics, Pleasanton, CA) following Manufacturer's instructions 3' gene expression libraries were constructed following 10x Genomics's instructions Libraries were sequenced on an Illumina NextSeq500 (Illumina Inc., San Diego, CA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX20355855" alias="GSM7350646_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX20355855</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7350646_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7350646: Kidney, rabrhabdomyolysis + CA3; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP437774">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP437774</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA972752</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17673249">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17673249</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7350646</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7350646</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>The single cell suspension with 95% viability was run on a 10x Chromium Single Cell instrument (10x Genomics, Pleasanton, CA) following Manufacturer's instructions 3' gene expression libraries were constructed following 10x Genomics's instructions Libraries were sequenced on an Illumina NextSeq500 (Illumina Inc., San Diego, CA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
