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Series GSE218987 Query DataSets for GSE218987
Status Public on May 24, 2023
Title CRISPR-based epigenome editing screens identify transcriptional and epigenetic regulators of human CD8 T cell function [ATAC-seq]
Organism Homo sapiens
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary Human CD8+ T cells were transduced with lentivirus encoding for HER2-CAR-2A-GFP or HER2-CAR-2A-BATF3.
T cells were either only stimulated once after thawing (acute stimulation) or repeatedly stimulated with HER2+ SKBR3 cells at a 1:2 effector to target (E:T) ratio every 3 days (chronic stimulation).
 
Overall design Comparative chromatin accessibility analysis of ATAC-seq data of acutely (n = 3) and chronically (n = 2) stimulated CD8+ T cells with or without BATF3 overexpression.
 
Contributor(s) McCutcheon SR, Gersbach CA
Citation(s) 37205457, 37945901
Submission date Nov 29, 2022
Last update date Dec 14, 2023
Contact name Sean McCutcheon
E-mail(s) sean.mccutcheon@duke.edu
Phone 7073447178
Organization name Duke University
Department Biomedical Engineering
Lab Charles Gersbach
Street address 101 Science Drive, CIEMAS Rm. 2323
City Durham
State/province NC
ZIP/Postal code 27708
Country USA
 
Platforms (1)
GPL30173 NextSeq 2000 (Homo sapiens)
Samples (10)
GSM6761476 CD8 T cells, GFP control, acute, donor 1, day 14
GSM6761477 CD8 T cells, GFP control, acute, donor 2, day 14
GSM6761478 CD8 T cells, GFP control, acute, donor 3, day 14
This SubSeries is part of SuperSeries:
GSE218988 CRISPR-based epigenome editing screens identify transcriptional and epigenetic regulators of human CD8 T cell function
Relations
BioProject PRJNA906521

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Supplementary file Size Download File type/resource
GSE218987_RAW.tar 1.4 Gb (http)(custom) TAR (of BW, NARROWPEAK)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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