GRNMOPT:基于多目标优化方法的基因调控网络推断

IF 2.6 4区 生物学 Q2 BIOLOGY
Heng Dong , Baoshan Ma , Yangyang Meng , Yiming Wu , Yongjing Liu , Tao Zeng , Jinyan Huang
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引用次数: 0

摘要

背景和目的重建基因调控网络(GRN)是破译复杂生物过程的重要方法。非线性常微分方程(ODEs)模型的应用已在预测基因调控网络方面显示出相当大的功效。值得注意的是,衰减率和时间延迟在真实基因调控中起着关键作用,但在 ODEs 模型中系统确定这两个参数的工作仍未得到充分探索。本研究介绍了 GRNMOPT,一种从时间序列和稳态数据推断 GRN 的创新方法。GRNMOPT 结合使用衰减率和时间延迟来构建 ODEs 模型,以真实地反映基因调控过程。它采用了一种多目标优化方法,同时优化衰减率和时间延迟,以得出这些因素的帕累托最优集,从而最大限度地提高准确度指标,如 AUROC(接收者工作特性曲线下面积)和 AUPR(精度-召回曲线下面积)。结果在 DREAM4 的两个模拟数据集和三个真实基因表达数据集(酵母、体内逆向工程和建模评估 [IRMA] 和大肠杆菌 [E.coli])上进行的综合实验评估显示,GRNMOPT 在不同网络规模下的表现都值得称赞。此外,交叉验证实验也证明了 GRNMOPT 的鲁棒性。 结论 我们提出了一种名为 GRNMOPT 的新方法,基于多目标优化框架推断 GRN,有效提高了推断的准确性,为 GRN 推断提供了有力的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
GRNMOPT: Inference of gene regulatory networks based on a multi-objective optimization approach

Background and objective

The reconstruction of gene regulatory networks (GRNs) stands as a vital approach in deciphering complex biological processes. The application of nonlinear ordinary differential equations (ODEs) models has demonstrated considerable efficacy in predicting GRNs. Notably, the decay rate and time delay are pivotal in authentic gene regulation, yet their systematic determination in ODEs models remains underexplored. The development of a comprehensive optimization framework for the effective estimation of these key parameters is essential for accurate GRN inference.

Method

This study introduces GRNMOPT, an innovative methodology for inferring GRNs from time-series and steady-state data. GRNMOPT employs a combined use of decay rate and time delay in constructing ODEs models to authentically represent gene regulatory processes. It incorporates a multi-objective optimization approach, optimizing decay rate and time delay concurrently to derive Pareto optimal sets for these factors, thereby maximizing accuracy metrics such as AUROC (Area Under the Receiver Operating Characteristic curve) and AUPR (Area Under the Precision-Recall curve). Additionally, the use of XGBoost for calculating feature importance aids in identifying potential regulatory gene links.

Results

Comprehensive experimental evaluations on two simulated datasets from DREAM4 and three real gene expression datasets (Yeast, In vivo Reverse-engineering and Modeling Assessment [IRMA], and Escherichia coli [E. coli]) reveal that GRNMOPT performs commendably across varying network scales. Furthermore, cross-validation experiments substantiate the robustness of GRNMOPT.

Conclusion

We propose a novel approach called GRNMOPT to infer GRNs based on a multi-objective optimization framework, which effectively improves inference accuracy and provides a powerful tool for GRNs inference.
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来源期刊
Computational Biology and Chemistry
Computational Biology and Chemistry 生物-计算机:跨学科应用
CiteScore
6.10
自引率
3.20%
发文量
142
审稿时长
24 days
期刊介绍: Computational Biology and Chemistry publishes original research papers and review articles in all areas of computational life sciences. High quality research contributions with a major computational component in the areas of nucleic acid and protein sequence research, molecular evolution, molecular genetics (functional genomics and proteomics), theory and practice of either biology-specific or chemical-biology-specific modeling, and structural biology of nucleic acids and proteins are particularly welcome. Exceptionally high quality research work in bioinformatics, systems biology, ecology, computational pharmacology, metabolism, biomedical engineering, epidemiology, and statistical genetics will also be considered. Given their inherent uncertainty, protein modeling and molecular docking studies should be thoroughly validated. In the absence of experimental results for validation, the use of molecular dynamics simulations along with detailed free energy calculations, for example, should be used as complementary techniques to support the major conclusions. Submissions of premature modeling exercises without additional biological insights will not be considered. Review articles will generally be commissioned by the editors and should not be submitted to the journal without explicit invitation. However prospective authors are welcome to send a brief (one to three pages) synopsis, which will be evaluated by the editors.
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