CaSNP: a database for interrogating copy number alterations of cancer genome from SNP array data

Cancer is known to have abundant copy number alterations (CNAs) that greatly contribute to its pathogenesis and progression. Investigation of CNA regions could potentially help identify oncogenes and tumor suppressor genes and infer cancer mechanisms. Although single-nucleotide polymorphism (SNP) ar...

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Bibliographic Details
Main Authors: Cao, Qingyi, Zhou, Meng, Wang, Xujun, Meyer, Cliff A., Zhang, Yong, Chen, Zhi, Li, Cheng, Liu, X. Shirley
Format: Artigo
Language:Inglês
Published: Oxford University Press 2011
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Articles
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC3013814/
https://ncbi.nlm.nih.gov/pubmed/20972221
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkq997
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