GSM2094821[Accession] - GEO DataSets

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Items: 3

Select item 2000794021.

CNV Identification: Prostate Cancer (PCa) vs Benign Prostatic Hyperplasia (BPH) Human DNA Samples

(Submitter supplied) Copy number variations (CNVs) in the human genome have been linked to various carcinomas including prostate cancer (PCa). This study was conducted to identify CNVs in high grade PCa. We performed a pilot genome-wide CNV analysis in 36 subjects (18 high grade PCa and 18 benign prostatic hyperplasia) using array comparative genomic hybridization (aCGH) technique. Array results were validated using PCR-based copy number counting method. more...

Organism:: Homo sapiens

Type:: Genome variation profiling by genome tiling array

Platform:: GPL10154
18 Samples

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Accession:: GSE79402

ID:: 200079402

Select item 1000101542.

Agilent-021365 SurePrint G3 Human CNV Microarray 2x400K (Feature Number version)

(Submitter supplied) Agilent's SurePrint G3 Human CNV Microarray, 2x400K Arrays of this design have barcodes that begin with 16021365 or 2521365. Data table annotations based on build hg18:NCBI36:Mar2006. Orientation: Features are numbered numbered Left-to-Right, Top-to-Bottom as scanned by an Agilent scanner (barcode on the left, DNA on the back surface, scanned through the glass), matching the FeatureNum output from Agilent's Feature Extraction software. more...