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Series GSE102097 Query DataSets for GSE102097
Status Public on Aug 22, 2017
Title VHL/HIF2a axis alters transcriptomic profiles in ccRCC
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary VHL loss is the most common genetic alteration event in ccRCC. VHL loss stabilizes hypoxia-inducible factor-2 alpha (HIF2a). We compared the changes in transcriptomics profiles after VHL restoration or HIF2a siRNA knockdown in 786-O cells.
 
Overall design RNA-seq profiles of ccRCC cell line 786-O with and without wild-type VHL restoration, with non-targeting control or pooled siRNA against HIF2a
 
Contributor(s) Yao X, Tan P
Citation(s) 28893800
Submission date Jul 31, 2017
Last update date Jul 25, 2021
Contact name Xiaosai Yao
E-mail(s) xiaosai.yao@gmail.com, yao.xiaosai@gene.com
Phone +65 68088271
Organization name Genome Institute of Singapore
Street address 60 Biopolis Street, Genome, #02-01
City Singapore
ZIP/Postal code 138672
Country Singapore
 
Platforms (1)
GPL11154 Illumina HiSeq 2000 (Homo sapiens)
Samples (4)
GSM2723874 786-O EV RNA-seq
GSM2723875 786-O VHL RNA-seq
GSM2723876 786-O NT RNA-seq
This SubSeries is part of SuperSeries:
GSE86095 VHL deficiency drives enhancer activation of oncogenes in clear cell renal cell carcinoma
Relations
BioProject PRJNA396577
SRA SRP114458

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE102097_RAW.tar 1.3 Gb (http)(custom) TAR (of BW)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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