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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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Bibliografske podrobnosti
Main Authors: Tran, Linh M, Zhang, Bin, Zhang, Zhan, Zhang, Chunsheng, Xie, Tao, Lamb, John R, Dai, Hongyue, Schadt, Eric E, Zhu, Jun
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2011
Teme:
Online dostop: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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