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Status |
Public on Aug 07, 2023 |
Title |
TooManyPeaks identifies drug-resistant-specific regulatory elements from single-cell leukemic epigenomes [ATAC-seq] |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
Purpose: To characterize epigenomic heterogeneity in GSI-responsive and -resistant T-ALL cells Method: We generated GSI-resistant T-ALL DND41 cells and profiled their epigenome using single-cell RNA sequencing. Result: We report here the presence of resistant-like subpopulation in drug naïve DND41 T-ALL cells. Conclusion: While other popular scRNA-seq clustering algorithms failed, TooManyPeaks, a suite of clustering and visualization algorithm developed in our lab, could identify rare resistant-like DND41 T-ALL cells.
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Overall design |
Single-cell ATAC-seq was performed on cells acquiring resistance to a gamma secretase inhibitor (GSI) after long-term treatment of Notch-mutated T-cell acute lymphoblastic leukemia (T-ALL) DND41 cells.
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Contributor(s) |
Zhou Y, Faryabi RB |
Citation missing |
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Submission date |
Aug 08, 2020 |
Last update date |
Aug 07, 2023 |
Contact name |
Robert Babak Faryabi |
E-mail(s) |
[email protected]
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Phone |
215-573-8220
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Organization name |
University of Pennsylvania
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Department |
Pathology
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Lab |
Faryabi Lab
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Street address |
Room 553 BRB II/III, 421 Curie Boulevard
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City |
Philadelphia |
State/province |
Pennsylvania |
ZIP/Postal code |
19104 |
Country |
USA |
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Platforms (1) |
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Samples (2) |
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Relations |
BioProject |
PRJNA656191 |
SRA |
SRP276947 |