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Status |
Public on Oct 26, 2018 |
Title |
Genome-wide maps of ONECUT2 binding sites in 22Rv1 human castration resistant prostate cancer cell |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
In order to determine whether ONECUT2 directly regulates the AR transcriptional program, or whether the effect of ONECUT2 is a mere consequence of AR downregulation, we performed ONECUT2 ChIP-sequencing (ChIP-seq) using the 22Rv1 human castration resistant prostate cancer cell line, which expresses high levels of ONECUT2 in comparison to other human prostate cancer cell lines
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Overall design |
Genome-wide binding profile of ONECUT2 transcription factor in 22Rv1 cell.
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Contributor(s) |
Freeman MR, Rotinen M, You S |
Citation(s) |
30478421 |
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Submission date |
Apr 09, 2017 |
Last update date |
May 15, 2019 |
Contact name |
Sungyong You |
E-mail(s) |
[email protected]
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Organization name |
Cedars-Sinai Medical Center
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Department |
Surgery
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Lab |
Freeman Lab.
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Street address |
Beverly Blvd 8400
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City |
LA |
State/province |
CA |
ZIP/Postal code |
90048 |
Country |
USA |
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Platforms (1) |
GPL21290 |
Illumina HiSeq 3000 (Homo sapiens) |
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Samples (4)
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Relations |
BioProject |
PRJNA382273 |
SRA |
SRP103756 |