ArticleScientific reports2015
Hidden Markov induced Dynamic Bayesian Network for recovering time evolving gene regulatory networks.
Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed.
- Uncovering Dynamic Neural Information Flow with Continuous-Time Weighted Dynamic Bayesian Networks.bioRxiv : the preprint server for biology · 2026Article
- Recovering time-varying networks from single-cell data.Bioinformatics (Oxford, England) · 2025Article
- Reconstructing Dynamic Gene Regulatory Networks Using f-Divergence from Time-Series scRNA-Seq Data.Current issues in molecular biology · 2025Article
- Review
- TGCnA: temporal gene coexpression network analysis using a low-rank plus sparse framework.Journal of applied statistics · 2020Article
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Authors and funding
2 authors.
Funding
Abstract
Dynamic Bayesian Networks (DBN) have been widely used to recover gene regulatory relationships from time-series data in computational systems biology. Its standard assumption is 'stationarity', and therefore, several research efforts have been recently proposed to relax this restriction. However, those methods suffer from three challenges: long running time, low accuracy and reliance on parameter settings. To address these problems, we propose a novel non-stationary DBN model by extending each hidden node of Hidden Markov Model into a DBN (called HMDBN), which properly handles the underlying time-evolving networks. Correspondingly, an improved structural EM algorithm is proposed to learn the HMDBN. It dramatically reduces searching space, thereby substantially improving computational efficiency. Additionally, we derived a novel generalized Bayesian Information Criterion under the non-stationary assumption (called BWBIC), which can help significantly improve the reconstruction accuracy and largely reduce over-fitting. Moreover, the re-estimation formulas for all parameters of our model are derived, enabling us to avoid reliance on parameter settings. Compared to the state-of-the-art methods, the experimental evaluation of our proposed method on both synthetic and real biological data demonstrates more stably high prediction accuracy and significantly improved computation efficiency, even with no prior knowledge and parameter settings.
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Registered trials
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