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Status |
Public on Mar 07, 2022 |
Title |
Peaksat: An R package for ChIP-seq peak saturation analysis |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
ChIP-Seq was performed on naiive cell lines from a Breast Cancer Progression model, including MCF10A, MCF10AT1, and DCIS. Biological replicates (n=2) were performed for all factors across all cell lines described.
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Overall design |
ChIP-Seq from a breast cancer progression cell model (including MCF10A, MCF10AT1, and DCIS)
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Contributor(s) |
Boyd J, Gao C, Quinn K, Fritz A, Glass K, Stein G, Frietze S |
Citation(s) |
36698077 |
Submission date |
Mar 04, 2022 |
Last update date |
Feb 08, 2023 |
Contact name |
Seth Frietze |
E-mail(s) |
Seth.Frietze@med.uvm.edu
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Organization name |
The University of Vermont
|
Department |
Biomedical and Health Sciences
|
Street address |
The University of Vermont
|
City |
Burtlington |
State/province |
VT |
ZIP/Postal code |
05405 |
Country |
USA |
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Platforms (1) |
GPL18460 |
Illumina HiSeq 1500 (Homo sapiens) |
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Samples (12)
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Relations |
Reanalysis of |
GSM1700382 |
Reanalysis of |
GSM1700383 |
BioProject |
PRJNA812937 |