Inference of time-delayed gene regulatory networks based on dynamic Bayesian network hybrid learning method

被引:10
|
作者
Yu, Bin [1 ,2 ,3 ]
Xu, Jia-Meng [1 ,3 ]
Li, Shan [1 ,3 ]
Chen, Cheng [1 ,3 ]
Chen, Rui-Xin [1 ,3 ]
Wang, Lei [4 ]
Zhang, Yan [3 ,5 ]
Wang, Ming-Hui [1 ,3 ]
机构
[1] Qingdao Univ Sci & Technol, Coll Math & Phys, Qingdao 266061, Peoples R China
[2] Univ Sci & Technol China, Dept Geophys & Planetary Sci, CAS Key Lab Geospace Environm, Hefei 230026, Anhui, Peoples R China
[3] Qingdao Univ Sci & Technol, Bioinformat & Syst Biol Res Ctr, Qingdao 266061, Peoples R China
[4] Qingdao Univ Sci & Technol, Coll Chem & Mol Engn, Lab Inorgan Synth & Appl Chem, Key Lab Ecochem Engn,Minist Educ, Qingdao 266042, Peoples R China
[5] Qingdao Univ Sci & Technol, Coll Electromech Engn, Qingdao 266061, Peoples R China
基金
中国国家自然科学基金;
关键词
gene regulatory networks; multiple time-delayed; dynamic Bayesian network; comprehensive score model; network structure profiles; REDUNDANCY REDUCTION; EXPRESSION; RECONSTRUCTION; IDENTIFICATION; INDUCTION; CYTOSCAPE; ALGORITHM; ACCURACY; MODELS;
D O I
10.18632/oncotarget.21268
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Gene regulatory networks (GRNs) research reveals complex life phenomena from the perspective of gene interaction, which is an important research field in systems biology. Traditional Bayesian networks have a high computational complexity, and the network structure scoring model has a single feature. Information-based approaches cannot identify the direction of regulation. In order to make up for the shortcomings of the above methods, this paper presents a novel hybrid learning method (DBNCS) based on dynamic Bayesian network (DBN) to construct the multiple time-delayed GRNs for the first time, combining the comprehensive score (CS) with the DBN model. DBNCS algorithm first uses CMI2NI (conditional mutual inclusive information-based network inference) algorithm for network structure profiles learning, namely the construction of search space. Then the redundant regulations are removed by using the recursive optimization algorithm (RO), thereby reduce the false positive rate. Secondly, the network structure profiles are decomposed into a set of cliques without loss, which can significantly reduce the computational complexity. Finally, DBN model is used to identify the direction of gene regulation within the cliques and search for the optimal network structure. The performance of DBNCS algorithm is evaluated by the benchmark GRN datasets from DREAM challenge as well as the SOS DNA repair network in Escherichia coli, and compared with other state-of-the-art methods. The experimental results show the rationality of the algorithm design and the outstanding performance of the GRNs.
引用
收藏
页码:80373 / 80392
页数:20
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