Comment[ArrayExpressAccession] E-GEOD-45000 MAGE-TAB Version 1.1 Public Release Date 2013-08-01 Investigation Title Genome-wide methylation analysis of prostate tissues reveals global methylation patterns of prostate cancer Comment[Submitted Name] Genome-wide methylation analysis of prostate tissues reveals global methylation patterns of prostate cancer Experiment Description High-throughput analyses of concordant gene methylation and expression events were carried out for 91 human prostate specimens, including prostate cancer (T), matched normal adjacent to tumor (AT), and organ donor (OD). Methylated DNA in genomic DNA was immunoprecipitated with anti-methylcytidine antibodies and detected by Affymetrix human whole genome SNP 6.0 chips. Methylated genomic DNA was purified by 5-hmc antibodies and Affymetrix SNP arrays were performed according to the manufacturer's manual. Copy number analysis of Affymetrix human SNP arrays was performed for both 5mc- and genomic DNA of prostate cancer samples. Methylations of genes were called when the allel amplification was reported in 5_mc DNA, and the background of the detection was suppressed by matched DNA sample. we used copy number of each probe set as baseline to detect the enrichment of methylated DNA from the same sample. Therefore, each specimen has two arrays; one is straight copy number (*SNP.CEL), another methylation enriched DNA (*5MC_SNP.CEL). Each CNV probe is based on the design from Affymetrix but no SNP ID was assigned. Term Source Name ArrayExpress EFO Term Source File http://www.ebi.ac.uk/arrayexpress/ http://www.ebi.ac.uk/efo/efo.owl Person Last Name Yu Yu Luo Person First Name Yan P. Yan Jian-hua Person Mid Initials P Person Email ypyu@pitt.edu Person Affiliation University of Pittsburgh Person Address Pathology, University of Pittsburgh, 3550 Terrace st., Pittsburgh, PA, USA Person Roles submitter Protocol Name P-GSE45000-4 P-GSE45000-5 P-GSE45000-1 P-GSE45000-2 P-GSE45000-3 P-GSE45000-6 Protocol Description As per manufacturer (Affymetrix) DNA was restriction digested, methylated genomic DNA was immunoprecipitated and purified with 5-hmc antibody, PCR amplified, fragmented, labeled and hybridized to each array according to the manufacturer's instructions. Prostate tissues were microdissected to obtain T or N samples. Cell lines were grown according to standard conditions. Genomic DNA was extracted from microdissected prostate tissues using Qiagen DNA Blood Mini Kit. DNA quality and quantity was assessed using a Nanodrop Spectrophotometer. The Arrays were then washed using Affymetrix fluidics stations, and scanned using the Gene Chip Scanner 3000. Protocol Type labelling protocol hybridization protocol sample treatment protocol growth protocol nucleic acid extraction protocol array scanning protocol Experimental Factor Name SAMPLE TYPE TISSUE SUBTYPE Experimental Factor Type sample type tissue subtype Comment[SecondaryAccession] GSE45000 Comment[GEOReleaseDate] 2013-08-01 Comment[ArrayExpressSubmissionDate] 2013-03-11 Comment[GEOLastUpdateDate] 2013-08-03 Comment[AEExperimentType] methylation profiling by array Comment[AdditionalFile:Data1] GSE45000_copy_number.txt SDRF File E-GEOD-45000.sdrf.txt