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Status |
Public on May 20, 2016 |
Title |
AR and ERG ChIP-seq in presence or absence of PRMT5 |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
Replicates of ChIP seq data using AR and ERG antibodies from VCaP cell lines harboring inducible shRNA constructs for PRMT5 (3 independent, sh1, sh2, sh3) and 1 non targeting control (NTC), all sample stimulated with ligand, either DHT or R1881
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Overall design |
AR ChIPseq in VCaP cells, 3 replicates each of DHT stimulated cells with one of 4 inducible shRNA constructs, sh1, sh2, sh3 targeting PRMT5 or NTC non targeting controls. Furthermore 2 AR ChIPseq in the same system stimulated with R1881 for targeting constructs sh1, sh2 and NTC. ERG ChIPseq 2 replicates DHT stimulated, each of sh1, sh2, sh3 constructs. Cells where induced (doxycyclin) for shRNA expression on day0, hormone starved on day3 and harvested on day5.
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Contributor(s) |
Westerling T, Mounir Z, Pagliarini R, Brown M |
Citation(s) |
27183006 |
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Submission date |
Mar 11, 2016 |
Last update date |
May 15, 2019 |
Contact name |
Thomas Westerling |
E-mail(s) |
thomas_westerling@dfci.harvard.edu
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Organization name |
Dana Farber Cancer institute
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Department |
Medical Oncology
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Lab |
Myles Brown
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Street address |
450 Brookline Ave
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City |
Boston |
State/province |
MA |
ZIP/Postal code |
02215 |
Country |
USA |
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Platforms (1) |
GPL18573 |
Illumina NextSeq 500 (Homo sapiens) |
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Samples (26)
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Relations |
BioProject |
PRJNA314989 |
SRA |
SRP071668 |