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Status |
Public on Aug 22, 2017 |
Title |
p53 ChIP-seq in Nutlin-treated HCT116, MCF7, and SJSA cell lines |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
To identify genomic loci occupied by p53, we performed p53 ChIP-seq analysis of colorectal carcinoma cell line HCT116, breast carcinoma line MCF7, and osteosarcoma line SJSA treated with MDM2 inhibitor Nutlin.
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Overall design |
HCT116, MCF7, and SJSA cells were treated with either DMSO or Nutlin for 12 hours. Samples from formaldehyde cross-linked cells were subjected to chromatin immunnoprecipitation and recovered DNA was sequenced.
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Contributor(s) |
Andrysik Z, Pandey A, Espinosa JM |
Citation(s) |
28904012 |
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Submission date |
Aug 29, 2016 |
Last update date |
May 15, 2019 |
Contact name |
Ahwan Pandey |
E-mail(s) |
ahwan.pandey@ucdenver.edu
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Organization name |
University of Colorado Anschutz Medical Center
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Department |
Pharmacology
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Lab |
Espinosa Lab
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Street address |
12800 E. 19th Ave.
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City |
Aurora |
State/province |
CO |
ZIP/Postal code |
80045 |
Country |
USA |
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Platforms (1) |
GPL16791 |
Illumina HiSeq 2500 (Homo sapiens) |
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Samples (9)
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GSM2296273 |
MCF7, ChIP-Seq, Input |
GSM2296274 |
MCF7, ChIP-Seq, DMSO treated |
GSM2296275 |
MCF7, ChIP-Seq, Nutlin treated |
GSM2296276 |
SJSA, ChIP-Seq, Input |
GSM2296277 |
SJSA, ChIP-Seq, DMSO treated |
GSM2296278 |
SJSA, ChIP-Seq, Nutlin treated |
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This SubSeries is part of SuperSeries: |
GSE86222 |
Identification of a core p53 transcriptional program with highly fractionated tumor suppressive activity |
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Relations |
BioProject |
PRJNA340392 |
SRA |
SRP083188 |
Supplementary file |
Size |
Download |
File type/resource |
GSE86164_RAW.tar |
3.3 Gb |
(http)(custom) |
TAR (of BIGWIG) |
SRA Run Selector |
Raw data are available in SRA |
Processed data provided as supplementary file |
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