Due to the tremendous heterogeneity of disease manifestations, many complex diseases that were once thought to be single diseases are now considered to have disease subtypes. Disease subtyping analysis, that is the identification of subgroups of patients with similar characteristics, is the first step to accomplish precision medicine. With the advancement of high-throughput technologies, omics data offers unprecedented opportunity to reveal disease subtypes. As a result, unsupervised clustering analysis has been widely used for this purpose. Though promising, the subtypes obtained from traditional quantitative approaches may not always be clinically meaningful (i.e. correlate with clinical outcomes). On the other hand, the collection of rich clinical data in modern epidemiology studies has the great potential to facilitate the disease subtyping process via omics data and to discovery clinically meaningful disease subtypes. Thus, we developed an outcome-guided Bayesian clustering (GuidedBayesianClustering) method to fully integrate the clinical data and the high-dimensional omics data. A Gaussian mixed model framework was applied to perform sample clustering; a spike-and-slab prior was utilized to perform gene selection; a mixture model prior was employed to incorporate the guidance from a clinical outcome variable; and a decision framework was adopted to infer the false discovery rate of the selected genes. We deployed conjugate priors to facilitate efficient Gibbs sampling. Our proposed full Bayesian method is capable of simultaneously (i) obtaining sample clustering (disease subtype discovery); (ii) performing feature selection (select genes related to the disease subtype); and (iii) utilizing clinical outcome variable to guide the disease subtype discovery. The superior performance of the GuidedBayesianClustering was demonstrated through simulations and applications of breast cancer expression data and Alzheimer's disease. An R package has been made publicly available on GitHub to improve the applicability of our method.
机构:
Guangdong Univ Technol, Sch Comp, Guangzhou 510006, Peoples R China
Tsinghua Univ, Dept Comp Sci & Technol, Beijing 100084, Peoples R ChinaGuangdong Univ Technol, Sch Comp, Guangzhou 510006, Peoples R China
Zeng, Yan
Hao, Zhifeng
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机构:
Shantou Univ, Coll Sci, Shantou 515063, Guangdong, Peoples R ChinaGuangdong Univ Technol, Sch Comp, Guangzhou 510006, Peoples R China
Hao, Zhifeng
Cai, Ruichu
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机构:
Guangdong Univ Technol, Sch Comp, Guangzhou 510006, Peoples R China
Pazhou Lab, Guangzhou 510006, Peoples R ChinaGuangdong Univ Technol, Sch Comp, Guangzhou 510006, Peoples R China
Cai, Ruichu
Xie, Feng
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机构:
Peking Univ, Sch Math Sci, Beijing 100084, Peoples R ChinaGuangdong Univ Technol, Sch Comp, Guangzhou 510006, Peoples R China
Xie, Feng
Huang, Libo
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机构:
Chinese Acad Sci, Inst Comp Technol, Beijing 100084, Peoples R ChinaGuangdong Univ Technol, Sch Comp, Guangzhou 510006, Peoples R China
Huang, Libo
Shimizu, Shohei
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机构:
Shiga Univ, Fac Data Sci, Hikone 5228522, Japan
RIKEN, Ctr Adv Intelligence Project AIP, Tokyo 1030027, JapanGuangdong Univ Technol, Sch Comp, Guangzhou 510006, Peoples R China