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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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखकों: Cao, Qingyi, Zhou, Meng, Wang, Xujun, Meyer, Cliff A., Zhang, Yong, Chen, Zhi, Li, Cheng, Liu, X. Shirley
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Oxford University Press 2011
विषय:
ऑनलाइन पहुंच: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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