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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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Detalhes bibliográficos
Main Authors: Cao, Qingyi, Zhou, Meng, Wang, Xujun, Meyer, Cliff A., Zhang, Yong, Chen, Zhi, Li, Cheng, Liu, X. Shirley
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2011
Assuntos:
Acesso em linha: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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