On Joint Estimation of Gaussian Graphical Models for Spatial and Temporal Data

被引:27
|
作者
Lin, Zhixiang [1 ,2 ]
Wang, Tao [3 ]
Yang, Can [4 ]
Zhao, Hongyu [5 ]
机构
[1] Yale Univ, Program Computat Biol & Bioinformat, New Haven, CT USA
[2] Stanford Univ, Dept Stat, Stanford, CA 94305 USA
[3] Shanghai Jiao Tong Univ, Dept Bioinformat & Biostat, Shanghai, Peoples R China
[4] Hong Kong Baptist Univ, Dept Math, Kowloon Tong, Hong Kong, Peoples R China
[5] Yale Univ, Sch Publ Hlth, Dept Biostat, New Haven, CT 06520 USA
基金
中国国家自然科学基金; 美国国家卫生研究院; 美国国家科学基金会;
关键词
Bayesian variable selection; Gaussian graphical model; Neighborhood selection; Markov random field; Spatial and temporal data; INVERSE COVARIANCE ESTIMATION; BAYESIAN VARIABLE SELECTION; REGULATION NETWORK; GENE-EXPRESSION; LASSO; TRANSCRIPTOME; INFERENCE; IDENTITY; NEURONS; TBR1;
D O I
10.1111/biom.12650
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In this article, we first propose a Bayesian neighborhood selection method to estimate Gaussian Graphical Models (GGMs). We show the graph selection consistency of this method in the sense that the posterior probability of the true model converges to one. When there are multiple groups of data available, instead of estimating the networks independently for each group, joint estimation of the networks may utilize the shared information among groups and lead to improved estimation for each individual network. Our method is extended to jointly estimate GGMs in multiple groups of data with complex structures, including spatial data, temporal data, and data with both spatial and temporal structures. Markov random field (MRF) models are used to efficiently incorporate the complex data structures. We develop and implement an efficient algorithm for statistical inference that enables parallel computing. Simulation studies suggest that our approach achieves better accuracy in network estimation compared with methods not incorporating spatial and temporal dependencies when there are shared structures among the networks, and that it performs comparably well otherwise. Finally, we illustrate our method using the human brain gene expression microarray dataset, where the expression levels of genes are measured in different brain regions across multiple time periods.
引用
收藏
页码:769 / 779
页数:11
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