Bayesian Graphical Models for Differential Pathways

被引:20
作者
Mitra, Riten [1 ]
Mueller, Peter [2 ]
Ji, Yuan [3 ]
机构
[1] Univ Louisville, Dept Biostat, Louisville, KY 40292 USA
[2] Univ Texas Austin, Dept Math, Austin, TX 78712 USA
[3] Northshore Univ HealthSyst, Ctr Clin & Res Informat, Glenview, IL 60026 USA
来源
BAYESIAN ANALYSIS | 2016年 / 11卷 / 01期
关键词
autologistic regression; histone modifications; Markov random fields; networks; reverse phase protein arrays; INVERSE WISHART DISTRIBUTIONS; HISTONE MODIFICATIONS; VARIABLE-SELECTION; HUMAN GENOME; METHYLATIONS; SIMULATION; INFERENCE; LASSO;
D O I
10.1214/14-BA931
中图分类号
O1 [数学];
学科分类号
0701 ; 070101 ;
摘要
Graphical models can be used to characterize the dependence structure for a set of random variables. In some applications, the form of dependence varies across different subgroups. This situation arises, for example, when protein activation on a certain pathway is recorded, and a subgroup of patients is characterized by a pathological disruption of that pathway. A similar situation arises when one subgroup of patients is treated with a drug that targets that same pathway. In both cases, understanding changes in the joint distribution and dependence structure across the two subgroups is key to the desired inference. Fitting a single model for the entire data could mask the differences. Separate independent analyses, on the other hand, could reduce the effective sample size and ignore the common features. In this paper, we develop a Bayesian graphical model that addresses heterogeneity and implements borrowing of strength across the two subgroups by simultaneously centering the prior towards a global network. The key feature is a hierarchical prior for graphs that borrows strength across edges, resulting in a comparison of pathways across subpopulations (differential pathways) under a unified model-based framework. We apply the proposed model to data sets from two very different studies: histone modifications from ChIP-seq experiments, and protein measurements based on tissue microarrays.
引用
收藏
页码:99 / 124
页数:26
相关论文
共 52 条
[1]  
[Anonymous], J AM STAT ASS
[2]   Monte Carlo method for computing the marginal likelihood in nondecomposable Gaussian graphical models [J].
Atay-Kayis, A ;
Massam, H .
BIOMETRIKA, 2005, 92 (02) :317-335
[3]  
Atchade Y., 2008, TECHNICAL REPORT, P107
[4]   High-resolution profiling of histone methylations in the human genome [J].
Barski, Artern ;
Cuddapah, Suresh ;
Cui, Kairong ;
Roh, Tae-Young ;
Schones, Dustin E. ;
Wang, Zhibin ;
Wei, Gang ;
Chepelev, Iouri ;
Zhao, Keji .
CELL, 2007, 129 (04) :823-837
[5]  
BESAG J, 1974, J ROY STAT SOC B MET, V36, P192
[6]   Objective Bayesian model selection in Gaussian graphical models [J].
Carvalho, C. M. ;
Scott, J. G. .
BIOMETRIKA, 2009, 96 (03) :497-512
[7]   Simulation of hyper-inverse Wishart distributions in graphical models [J].
Carvalho, Carlos M. ;
Massam, Helene ;
West, Mike .
BIOMETRIKA, 2007, 94 (03) :647-659
[8]  
Chen MH, 1997, ANN STAT, V25, P1563
[9]  
Chen Ming-Hui., 2000, Monte Carlo Methods in Bayesian Computation, P213, DOI [DOI 10.1007/978-1-4612-1276-8, 10.1007/978-1-4612-1276-87]
[10]  
Chen S., 2013, ARXIV13110085