<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX17953348" alias="GSM6658038_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17953348</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6658038_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6658038: healthy control PBMC; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP403429">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP403429</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA892009</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15470534">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15470534</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6658038</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6658038</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>Peripheral blood was drawn from each patient and volunteer into a tube containing EDTA-2Na and centrifuged to separate PBMCs and frozen. All samples were thawed on same day and immediately processed 10x Genomics Gene Expression 3' Chromium V 2.0 per manufacturer's instructions. A single cell suspension was obtained by filtering with a 40 μm cell strainer. Library preparation were performed with the Single Cell 3' Library &amp; Gel Bead Kit v3.1 according to the 10X Genomics' standard protocol.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17953349" alias="GSM6658039_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17953349</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6658039_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6658039: Autoimmune hepatitis patient PBMC; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP403429">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP403429</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA892009</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15470535">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15470535</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6658039</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6658039</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>Peripheral blood was drawn from each patient and volunteer into a tube containing EDTA-2Na and centrifuged to separate PBMCs and frozen. All samples were thawed on same day and immediately processed 10x Genomics Gene Expression 3' Chromium V 2.0 per manufacturer's instructions. A single cell suspension was obtained by filtering with a 40 μm cell strainer. Library preparation were performed with the Single Cell 3' Library &amp; Gel Bead Kit v3.1 according to the 10X Genomics' standard protocol.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
