GENE NETWORK RECONSTRUCTION USING GLOBAL-LOCAL SHRINKAGE PRIORS

被引:14
|
作者
Leday, Gwenael G. R. [1 ]
de Gunst, Mathisca C. M. [2 ]
Kpogbezan, Gino B. [3 ]
van der Vaart, Aad W. [3 ]
van Wieringen, Wessel N. [2 ,4 ]
van de Wiel, Mark A. [2 ,4 ]
机构
[1] Univ Cambridge, Cambridge Inst Publ Hlth, Sch Clin Med, MRC Biostat Unit, Forvie Site,Robinson Way,Cambridge Biomed Campus, Cambridge CB2 0SR, England
[2] Vrije Univ Amsterdam, Dept Math, De Boelelaan 1081, NL-1081 HV Amsterdam, Netherlands
[3] Leiden Univ, Fac Sci, Math Inst, POB 9512, NL-2300 RA Leiden, Netherlands
[4] Vrije Univ Amsterdam Med Ctr, Dept Epidemiol & Biostat, POB 7057, NL-1007 MB Amsterdam, Netherlands
来源
ANNALS OF APPLIED STATISTICS | 2017年 / 11卷 / 01期
关键词
Undirected gene network; Bayesian inference; shrinkage; variational approximation; empirical Bayes; COVARIANCE-MATRIX ESTIMATION; TUNING PARAMETER SELECTION; VARIABLE SELECTION; BAYESIAN-INFERENCE; GRAPHICAL MODELS; VARIATIONAL INFERENCE; EXPRESSION; CATHEPSINS; LIKELIHOOD;
D O I
10.1214/16-AOAS990
中图分类号
O21 [概率论与数理统计]; C8 [统计学];
学科分类号
020208 ; 070103 ; 0714 ;
摘要
Reconstructing a gene network from high-throughput molecular data is an important but challenging task, as the number of parameters to estimate easily is much larger than the sample size. A conventional remedy is to regularize or penalize the model likelihood. In network models, this is often done locally in the neighborhood of each node or gene. However, estimation of the many regularization parameters is often difficult and can result in large statistical uncertainties. In this paper we propose to combine local regularization with global shrinkage of the regularization parameters to borrow strength between genes and improve inference. We employ a simple Bayesian model with nonsparse, conjugate priors to facilitate the use of fast variational approximations to posteriors. We discuss empirical Bayes estimation of hyperparameters of the priors, and propose a novel approach to rank-based posterior thresholding. Using extensive model-and data-based simulations, we demonstrate that the proposed inference strategy outperforms popular (sparse) methods, yields more stable edges, and is more reproducible. The proposed method, termed ShrinkNet, is then applied to Glioblastoma to investigate the interactions between genes associated with patient survival.
引用
收藏
页码:41 / 68
页数:28
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