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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Detalles Bibliográficos
Autores principales: Cao, Qingyi, Zhou, Meng, Wang, Xujun, Meyer, Cliff A., Zhang, Yong, Chen, Zhi, Li, Cheng, Liu, X. Shirley
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2011
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3013814/
https://www.ncbi.nlm.nih.gov/pubmed/20972221
http://dx.doi.org/10.1093/nar/gkq997

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3013814/
https://www.ncbi.nlm.nih.gov/pubmed/20972221
http://dx.doi.org/10.1093/nar/gkq997

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