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Inferring causal genomic alterations in breast cancer using gene expression data

BACKGROUND: One of the primary objectives in cancer research is to identify causal genomic alterations, such as somatic copy number variation (CNV) and somatic mutations, during tumor development. Many valuable studies lack genomic data to detect CNV; therefore, methods that are able to infer CNVs f...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Tran, Linh M, Zhang, Bin, Zhang, Zhan, Zhang, Chunsheng, Xie, Tao, Lamb, John R, Dai, Hongyue, Schadt, Eric E, Zhu, Jun
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: BioMed Central 2011
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC3162519/
https://ncbi.nlm.nih.gov/pubmed/21806811
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1752-0509-5-121
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