<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE188319" accession="SRP344807">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP344807</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA778256</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE188319</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Population RNA-seq and ATAC-seq of SLAMF6+ and CXCR6+ Th17 cells</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Other"/>
      <STUDY_ABSTRACT>To characterize and validate the functional roles of the splenic SLAMF6+ and CXCR6+ Th17 cells during EAE, we performed population RNA-seq and ATAC-seq for wild type mice, as well as population RNA-seq for Il17aCre Il23rfl/fl knockout mice. Overall design: We isolated SLAMF6+ and CXCR6+ Th17 cells from the spleen during EAE for three independent experiments: (1) RNA-seq for cells from four Il17aCre tdTomato reporter mice; (2) ATAC-seq for cells from five Il17aCre tdTomato reporter mice. (3) RNA-seq for cells from four Il17aCre Il23rfl/fl (Il23r KO) vs. four Il17aCre Il23rWT (Il23r WT) mice.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE188319</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_LINKS>
      <STUDY_LINK>
        <XREF_LINK>
          <DB>pubmed</DB>
          <ID>34875227</ID>
        </XREF_LINK>
      </STUDY_LINK>
    </STUDY_LINKS>
    <STUDY_ATTRIBUTES>
      <STUDY_ATTRIBUTE>
        <TAG>parent_bioproject</TAG>
        <VALUE>PRJNA778252</VALUE>
      </STUDY_ATTRIBUTE>
    </STUDY_ATTRIBUTES>
  </STUDY>
</STUDY_SET>
