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Status |
Public on Jun 14, 2016 |
Title |
Genome-wide H3K4me3 after MK2206/DMSO treatment of T47D cells |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
We perfomed ChIP-seq using H3K4me3 antibodies in T47D cells after 24 hour treatment with the AKT inhibitor MK2206 or DMSO. We demonstrate that at a selected group of loci H3K4me3 is affected by AKT inhibition.
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Overall design |
Comparison of genome-wide H3K4me3 binding after AKT inhibition vs vehicle
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Contributor(s) |
Dreijerink K, Groner A, Spangle J |
Citation(s) |
27292631 |
Submission date |
Apr 22, 2016 |
Last update date |
May 15, 2019 |
Contact name |
Koen M.A. Dreijerink |
E-mail(s) |
koendreijerink@yahoo.com
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Organization name |
Dana-Farber Cancer Institute
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Department |
Medical Oncology
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Street address |
450 Brookline Avenue
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City |
Boston |
State/province |
MA |
ZIP/Postal code |
02215 |
Country |
USA |
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Platforms (2) |
GPL11154 |
Illumina HiSeq 2000 (Homo sapiens) |
GPL18573 |
Illumina NextSeq 500 (Homo sapiens) |
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Samples (6)
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This SubSeries is part of SuperSeries: |
GSE80594 |
PI3K/AKT signaling regulates H3K4 methylation in breast cancer |
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Relations |
BioProject |
PRJNA319401 |
SRA |
SRP073742 |