Information enhanced model selection for Gaussian graphical model with application to metabolomic data. (15th March 2021)

• Record Type: Journal Article
• Authors: Zhou, Jie; Hoen, Anne G; Mcritchie, Susan; Pathmasiri, Wimal; Viles, Weston D; Nguyen, Quang P; Madan, Juliette C; Dade, Erika; Karagas, Margaret R; Gui, Jiang
• Is Part Of: Biostatistics. Volume 23:Number 3(2022)
• Page Start: 926
• Page End: 948
• Publication Date: 2021-03-15
• Subjects: Chow–Liu algorithm -- Metabolite pathway analysis -- Model pool -- Prior structure -- Structural BIC -- Structure learning algorithm -- Two-step algorithm -- Undirected Gaussian graphical model; Medical statistics -- Periodicals; Biometry -- Periodicals; Health risk assessment -- Periodicals; Medicine -- Research -- Statistical methods -- Periodicals; 610.727
• DOI: 10.1093/biostatistics/kxab006
• Languages: English
• ISSNs: 1465-4644

Abstract

Summary: In light of the low signal-to-noise nature of many large biological data sets, we propose a novel method to learn the structure of association networks using Gaussian graphical models combined with prior knowledge. Our strategy includes two parts. In the first part, we propose a model selection criterion called structural Bayesian information criterion, in which the prior structure is modeled and incorporated into Bayesian information criterion. It is shown that the popular extended Bayesian information criterion is a special case of structural Bayesian information criterion. In the second part, we propose a two-step algorithm to construct the candidate model pool. The algorithm is data-driven and the prior structure is embedded into the candidate model automatically. Theoretical investigation shows that under some mild conditions structural Bayesian information criterion is a consistent model selection criterion for high-dimensional Gaussian graphical model. Simulation studies validate the superiority of the proposed algorithm over the existing ones and show the robustness to the model misspecification. Application to relative concentration data from infant feces collected from subjects enrolled in a large molecular epidemiological cohort study validates that metabolic pathway involvement is a statistically significant factor for the conditional dependence between metabolites. Furthermore, new relationships among metabolites are discovered which can not be identified by the conventional methods of pathway analysis. Some of them have been widely recognized in biological literature.