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Status |
Public on Oct 15, 2018 |
Title |
RNA-seq analysis of BAP1-depleted uveal melanoma cells |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by high throughput sequencing
|
Summary |
OCM-1A uveal melanoma cells were infected with lentivirus carrying shRNA expression constructs specific for BAP1 or GFP (control), and placed under selection for 6 days. RNA-seq was performed.
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Overall design |
Samples represent three independent experiments treated with control or BAP1 shRNA
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Contributor(s) |
Onken MD, Yen M |
Citation(s) |
30400891 |
NIH grant(s) |
Grant ID |
Grant title |
Affiliation |
Name |
R01 GM038542 |
ACTIN AND MICROTUBULE-BASED MECHANISMS FOR FUNCTIONS OF NK LYMPHOID CELLS |
WASHINGTON UNIVERSITY |
JOHN A COOPER |
R35 GM118171 |
ACTIN ASSEMBLY AND CELL MOTILITY: MECHANISMS AND REGULATION |
WASHINGTON UNIVERSITY |
JOHN A COOPER |
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Submission date |
Feb 06, 2018 |
Last update date |
Mar 27, 2019 |
Contact name |
Michael D Onken |
Organization name |
Washington University School of Medicine
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Department |
Biochemistry & Molecular Biophysics
|
Lab |
Box 8231
|
Street address |
660 S. Euclid Ave
|
City |
Saint Louis |
State/province |
MO |
ZIP/Postal code |
63110 |
Country |
USA |
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Platforms (1) |
GPL16791 |
Illumina HiSeq 2500 (Homo sapiens) |
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Samples (6)
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Relations |
BioProject |
PRJNA433106 |
SRA |
SRP132263 |