<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX18025336" alias="GSM6679417_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18025336</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6679417_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6679417: KO_gingiva infiltration immune cells; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP404534">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP404534</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA894293</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15532975">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15532975</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6679417</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6679417</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>Single cells were mixed with Gel Beads, Partitioning Oil and glycerol, using for preparation of GEMs with ChromiumTM Next GEM Chip G Single Cell Kit. The GEMs were subjected to RT-PCR, and the products were purified with Dynabeads, followed by cDNA amplification. RNA libraries were prepared with ChromiumTM Next GEM Single Cell 3' GEM, Library &amp; Gel Bead Kit v3.1 according to the manufacturer's protocol.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18025337" alias="GSM6679416_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18025337</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6679416_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6679416: WT_gingiva infiltration immune cells; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP404534">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP404534</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA894293</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15532974">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15532974</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6679416</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6679416</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>Single cells were mixed with Gel Beads, Partitioning Oil and glycerol, using for preparation of GEMs with ChromiumTM Next GEM Chip G Single Cell Kit. The GEMs were subjected to RT-PCR, and the products were purified with Dynabeads, followed by cDNA amplification. RNA libraries were prepared with ChromiumTM Next GEM Single Cell 3' GEM, Library &amp; Gel Bead Kit v3.1 according to the manufacturer's protocol.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
