Large-scale dynamic gene regulatory network inference combining differential equation models with local dynamic Bayesian network analysis

被引:60
|
作者
Li, Zheng [1 ]
Li, Ping [1 ]
Krishnan, Arun [2 ]
Liu, Jingdong [1 ]
机构
[1] Monsanto Co, Chesterfield, MO 63017 USA
[2] Monsanto Res Ctr, Bangalore 560092, Karnataka, India
关键词
CELL-CYCLE; COMPOUND-MODE; EXPRESSION; BRCA1; IDENTIFICATION;
D O I
10.1093/bioinformatics/btr454
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: Reverse engineering gene regulatory networks, especially large size networks from time series gene expression data, remain a challenge to the systems biology community. In this article, a new hybrid algorithm integrating ordinary differential equation models with dynamic Bayesian network analysis, called Differential Equation-based Local Dynamic Bayesian Network (DELDBN), was proposed and implemented for gene regulatory network inference. Results: The performance of DELDBN was benchmarked with an in vivo dataset from yeast. DELDBN significantly improved the accuracy and sensitivity of network inference compared with other approaches. The local causal discovery algorithm implemented in DELDBN also reduced the complexity of the network inference algorithm and improved its scalability to infer larger networks. We have demonstrated the applicability of the approach to a network containing thousands of genes with a dataset from human HeLa cell time series experiments. The local network around BRCA1 was particularly investigated and validated with independent published studies. BRAC1 network was significantly enriched with the known BRCA1-relevant interactions, indicating that DELDBN can effectively infer large size gene regulatory network from time series data.
引用
收藏
页码:2686 / 2691
页数:6
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