NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM7791670 Query DataSets for GSM7791670
Status Public on Sep 19, 2023
Title Pool3-RNA-multiome
Sample type SRA
 
Source name tissue resident memory T cells
Organism Mus musculus
Characteristics tissue: Liver + Spleen
days p.i.: 14
replicate: 1
Extracted molecule total RNA
Extraction protocol Nuclei were isolated from frozen, flow cytometry sorted CD8+ T cell subsets
scATAC-seq libraries were constructed using 10X genomics reagents and protocols
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina NovaSeq 6000
 
Data processing Multiome fastq files were processed using CellRanger-ARC pipeline v2
After read alignment with bwa for ATAC, fragment files were generated by offsetting Tn5 inserts and deduplicating
After read alignment with STAR for RNA, a cell x genes count matrix was generated using the featureCounts options
Assembly: mm10
Supplementary files format and content: fragments file containing trimmed, deduplicated, high quality atac-seq fragments and cell barcodes; h5 files containing the cell x feature matrices
 
Submission date Sep 19, 2023
Last update date Sep 20, 2023
Contact name Caleb Lareau
E-mail(s) lareauc@mskcc.org
Organization name Memorial Sloan Kettering
Street address 417 E 68th St, Zuckerman - ZRC 1132
City New York
State/province New York
ZIP/Postal code 10065
Country USA
 
Platform ID GPL24247
Series (2)
GSE243593 A unique epigenomic landscape defines CD8+ tissue-resident memory T cells [multiome]
GSE243597 A unique epigenomic landscape defines CD8+ tissue-resident memory T cells
Relations
BioSample SAMN37472244
SRA SRX21828307

Supplementary file Size Download File type/resource
GSM7791670_pool3_filtered_feature_bc_matrix.h5 15.6 Mb (ftp)(http) H5
SRA Run SelectorHelp
Raw data are available in SRA

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap