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Article

Detection of prostate cancer related copy number variations with SNP genotyping array.

European review for medical and pharmacological sciences - 1 Nov 2013

Wang Y, Yao X, Li S-N, Suo A-L, Tian T, Ruan Z-P, Guo H, Yao Y

Abstract excerpt

AIM: Prostate cancer is characterized by the accumulation of multiple copy number variants (CNVs) across the genome. We aim to identify potential prostate cancer related CNVs. MATERIALS AND METHODS: Whole-genome SNP genotyping data of 18 prostate cancer patients was downloaded from the GEO (Gene Expression Omnibus) database. PennCNV was used to detect CNVs. All genes and miRNAs affected by CNVs were annotated. We...

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PMID: 24254561

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