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Status |
Public on Dec 28, 2016 |
Title |
SOX9 Drives WNT Pathway Activation in Prostate Cancer [ChIP-seq] |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
SOX9 is critical for prostate development and is implicated in prostate cancer, we used SOX9 ChIP-seq in combination with transcriptome profiling to identify genes and pathways it regulates in normal or neoplastic epithelium.
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Overall design |
Chromatin was immunoprecipitated by SOX9 antibody in the TMPRSS2-ERG fusion positive prostate cancer cell line VCaP with high basal SOX9 expression and submitted for high throughput sequencing in parallel with input control.
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Contributor(s) |
Ma F, Yuan X, Balk SP |
Citation(s) |
27043282 |
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Submission date |
Dec 31, 2015 |
Last update date |
May 15, 2019 |
Contact name |
Fen Ma |
E-mail(s) |
fenmag@gmail.com
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Organization name |
BIDMC
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Department |
Hem/Onc
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Lab |
Balk lab
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Street address |
3 Blackfan Circle
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City |
Boston |
State/province |
MA |
ZIP/Postal code |
02115 |
Country |
USA |
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Platforms (1) |
GPL11154 |
Illumina HiSeq 2000 (Homo sapiens) |
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Samples (2) |
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This SubSeries is part of SuperSeries: |
GSE76452 |
SOX9 Drives WNT Pathway Activation in Prostate Cancer |
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Relations |
BioProject |
PRJNA307344 |
SRA |
SRP067970 |