Identification of Risk Pathways and Functional Modules for Coronary Artery Disease Based on Genome-wide SNP Data

Coronary artery disease (CAD) is a complex human disease, involving multiple genes and their nonlinear interactions, which often act in a modular fashion. Genome-wide single nucleotide polymorphism (SNP) profiling provides an effective technique to unravel these underlying genetic interplays or thei...

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Detalhes bibliográficos
Publicado no:Genomics Proteomics Bioinformatics
Main Authors: Zhao, Xiang, Luan, Yi-Zhao, Zuo, Xiaoyu, Chen, Ye-Da, Qin, Jiheng, Jin, Lv, Tan, Yiqing, Lin, Meihua, Zhang, Naizun, Liang, Yan, Rao, Shao-Qi
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2016
Assuntos:
Original Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5200919/
https://ncbi.nlm.nih.gov/pubmed/27965104
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.gpb.2016.04.008
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