Adaptive modelling of gene regulatory network using Bayesian information criterion-guided sparse regression approach

被引:6
作者
Shi, Ming [1 ,2 ]
Shen, Weiming [2 ]
Wang, Hong-Qiang [1 ]
Chong, Yanwen [2 ]
机构
[1] Chinese Acad Sci, Inst Intelligent Machines, Machine Intelligence & Computat Biol Lab, POB 1130, Hefei 230031, Peoples R China
[2] Wuhan Univ, State Key Lab Informat Engn Surveying Mapping & R, 129 Luoyu Rd, Wuhan 430079, Peoples R China
基金
中国国家自然科学基金;
关键词
genetics; Bayes methods; genomics; regression analysis; inference mechanisms; bioinformatics; adaptive modelling; gene regulatory network; Bayesian information criterion-guided sparse regression approach; GRN; microarray expression data; systems biology; GRN reconstruction; optimisation; l(1)-norm regularisation; TRANSCRIPTION FACTOR; SELECTION; IDENTIFICATION; LASSO;
D O I
10.1049/iet-syb.2016.0005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Inferring gene regulatory networks (GRNs) from microarray expression data are an important but challenging issue in systems biology. In this study, the authors propose a Bayesian information criterion (BIC)-guided sparse regression approach for GRN reconstruction. This approach can adaptively model GRNs by optimising the l(1)-norm regularisation of sparse regression based on a modified version of BIC. The use of the regularisation strategy ensures the inferred GRNs to be as sparse as natural, while the modified BIC allows incorporating prior knowledge on expression regulation and thus avoids the overestimation of expression regulators as usual. Especially, the proposed method provides a clear interpretation of combinatorial regulations of gene expression by optimally extracting regulation coordination for a given target gene. Experimental results on both simulation data and real-world microarray data demonstrate the competent performance of discovering regulatory relationships in GRN reconstruction.
引用
收藏
页码:252 / 259
页数:8
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