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Series GSE143645 Query DataSets for GSE143645
Status Public on Jan 15, 2020
Title Joint Profiling of Chromatin Accessibility and CAR-T Integration Site Analysis at Population and Single-cell Levels I
Organism Homo sapiens
Experiment type Other
Genome binding/occupancy profiling by high throughput sequencing
Summary We report the development of a novel method called EpiVIA (https://github.com/VahediLab/epiVIA) for the joint profiling of the chromatin accessibility and lentiviral integration site analysis at the population and single-cell levels. We validate our technique in clonal cells with previously defined integration sites and further demonstrate the ability to measure lentiviral integration sites and chromatin accessibility of host and viral genomes at the single-cell resolution in CAR-T cells. We anticipate that EpiVIA will enable the single-cell deconstruction of gene regulation during CAR-T therapy, leading to the discovery of cellular factors associated with durable treatment.
 
Overall design Idenfification of integration sites in two clonal cells with ATAC-seq.
 
Contributor(s) Wang W, Vahedi G
Citation(s) 32094195
Submission date Jan 14, 2020
Last update date Mar 30, 2020
Contact name Wenliang Wang
E-mail(s) [email protected]
Organization name University of Pennsylvania
Street address 421 Curie Boulevard
City Philadelphia
State/province PENNSYLVANIA
ZIP/Postal code 19104
Country USA
 
Platforms (1)
GPL21697 NextSeq 550 (Homo sapiens)
Samples (2)
GSM4271121 clone 1
GSM4271122 clone 2
This SubSeries is part of SuperSeries:
GSE143647 Joint Profiling of Chromatin Accessibility and CAR-T Integration Site Analysis at Population and Single-cell Levels
Relations
BioProject PRJNA601178
SRA SRP241923

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
GSE143645_RAW.tar 10.0 Kb (http)(custom) TAR (of TXT)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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