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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
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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.
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Overall design |
The transcriptome profiles of cells with the same targeting gRNA were compared to cells with only non-targeting gRNAs.
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Contributor(s) |
McCutcheon SR, Gersbach CA |
Citation(s) |
37205457, 37945901 |
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Submission date |
Nov 29, 2022 |
Last update date |
Dec 14, 2023 |
Contact name |
Sean McCutcheon |
E-mail(s) |
sean.mccutcheon@duke.edu
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Phone |
7073447178
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Organization name |
Duke University
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Department |
Biomedical Engineering
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Lab |
Charles Gersbach
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Street address |
101 Science Drive, CIEMAS Rm. 2323
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City |
Durham |
State/province |
NC |
ZIP/Postal code |
27708 |
Country |
USA |
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Platforms (1) |
GPL24676 |
Illumina NovaSeq 6000 (Homo sapiens) |
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Samples (6)
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This SubSeries is part of SuperSeries: |
GSE218988 |
CRISPR-based epigenome editing screens identify transcriptional and epigenetic regulators of human CD8 T cell function |
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Relations |
BioProject |
PRJNA906519 |