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Series GSE30336 Query DataSets for GSE30336
Status Public on Feb 16, 2012
Title Expression analysis of 52 glioma clinical samples (36 CIMP+ and 16 CIMP-) and 6 cell line samples
Organism Homo sapiens
Experiment type Expression profiling by array
Summary Glioma CIMP (G-CIMP) is a powerful determinant of tumor pathogenicity but the molecular cause of G-CIMP is a fundamental question that is unresolved. Here, we show that mutation of a single gene, isocitrate dehydrogenase 1 (IDH1), directly causes the G-CIMP in gliomas by remodeling the methylome.
 
Overall design In this study 52 glioma clinic samples (36 CIMP+ and 16 CIMP-) were analyzed. Parental IDH1 wild-type and IDH1 mutant cells were passaged 40 and passage 40 were cell line was sent for expression array.
 
Contributor(s) Fang F, Chan T
Citation(s) 22343889, 27165745
Submission date Jun 30, 2011
Last update date Oct 04, 2019
Contact name FANG FANG
E-mail(s) fangf100088@gmail.com
Phone 646-8882783
Fax 646-8882595
Organization name Memorial Sloan-Kettering Cancer Center
Department The Human Oncology and Pathogenesis Program
Lab Timothy Chan
Street address 1275 York Avenue
City New York
State/province NY
ZIP/Postal code 10065
Country USA
 
Platforms (2)
GPL570 [HG-U133_Plus_2] Affymetrix Human Genome U133 Plus 2.0 Array
GPL571 [HG-U133A_2] Affymetrix Human Genome U133A 2.0 Array
Samples (58)
GSM752089 Tumor ID 21
GSM752090 Tumor ID 18
GSM752091 Tumor ID 19
This SubSeries is part of SuperSeries:
GSE30339 IDH1 Mutation is a Master Regulator of Epigenomic Remodeling and is Sufficient to Establish the Glioma Hypermethylator Phenotype
Relations
BioProject PRJNA154809

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
GSE30336_RAW.tar 122.9 Mb (http)(custom) TAR (of CEL)
Processed data included within Sample table

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