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Series GSE202335 Query DataSets for GSE202335
Status Public on May 05, 2022
Title H3K9 methylation drives resistance to androgen receptor–antagonist therapy in prostate cancer
Organism Homo sapiens
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary The study was performed to identify the role of H3K9 methylation in prostate cancer. This experiment was conducted to determine the genomic localization of H3K9me2 and H3K9me3 in naïve, short-term antiandrogen treated and antiandrogen resistant prostate cancer cells.
 
Overall design Chromatin immunoprecipitation DNA-sequencing (ChIP-seq) for histone modifications H3K9me2 and H3K9me3 in naïve LNCaP, short-term antiandrogen treated LNCaP and LNCaP EnzR cells.
 
Contributor(s) Baratchian M, Tiwari R, Sharifi N
Citation(s) 35584120
Submission date May 05, 2022
Last update date Jun 23, 2022
Contact name Vladimir Makarov
E-mail(s) makarov@ccf.org
Phone 2162879971
Organization name CLEVELAND CLINIC LERNER COM-CWRU
Street address 9500 Euclid Ave
City Cleveland
State/province OH
ZIP/Postal code 44195
Country USA
 
Platforms (1)
GPL18573 Illumina NextSeq 500 (Homo sapiens)
Samples (8)
GSM6108627 LNCaP_Pooled_Input_1
GSM6108628 LNCaP_Pooled_Input_2
GSM6108629 LNCaP_Parental_H3K9me2
Relations
BioProject PRJNA835482

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
GSE202335_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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