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Series GSE218985 Query DataSets for GSE218985
Status Public on May 24, 2023
Title CRISPR-based epigenome editing screens identify transcriptional and epigenetic regulators of human CD8 T cell function [CRISPRi/a TF scRNA-seq characterization]
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Other
Summary Human CD8+CCR7+ T cells from three donors were transduced with CRISPRi and CRISPRa TF gRNA libraries and expanded for 10 days. After 10 days, we used single-cell RNA sequencing (scRNA-seq) to analyze the transcriptomic effects of silencing or activating each gene candidate.
 
Overall design The transcriptome profiles of cells with the same targeting gRNA were compared to cells with only non-targeting gRNAs.
 
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)
GPL24676 Illumina NovaSeq 6000 (Homo sapiens)
Samples (6)
GSM6761464 TF CRISPRi screen donor 1, day 10
GSM6761465 TF CRISPRi screen donor 2, day 10
GSM6761466 TF CRISPRi screen donor 3, day 10
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 PRJNA906519

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE218985_RAW.tar 1.9 Gb (http)(custom) TAR (of TAR)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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