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Bayesian Data Fusion of Gene Expression and Histone Modification Profiles for Inference of Gene Regulatory Network.
IEEE/ACM Transactions on Computational Biology and Bioinformatics ( IF 4.5 ) Pub Date : 2018-09-10 , DOI: 10.1109/tcbb.2018.2869590
Haifen Chen , D. A. K. Maduranga , Piyushkumar A. Mundra , Jie Zheng

Accurately reconstructing gene regulatory networks (GRNs) from high-throughput gene expression data has been a major challenge in systems biology for decades. Many approaches have been proposed to solve this problem. However, there is still much room for the improvement of GRN inference. Integrating data from different sources is a promising strategy. Epigenetic modifications have a close relationship with gene regulation. Hence, epigenetic data such as histone modification profiles can provide useful information for uncovering regulatory interactions between genes. In this paper, we propose a method to integrate epigenetic data into the inference of GRNs. In particular, a dynamic Bayesian network (DBN) is employed to infer gene regulations from time-series gene expression data. Epigenetic data (histone modification profiles here) are integrated into the prior probability distribution of the Bayesian model. Our method has been validated on both synthetic and real datasets. Experimental results show that the integration of epigenetic data can significantly improve the performance of GRN inference. As more epigenetic datasets become available, our method would be useful for elucidating the gene regulatory mechanisms driving various cellular activities. The source code and testing datasets are available at https://github.com/Zheng-Lab/MetaGRN/tree/master/histonePrior.

中文翻译:

基因表达和组蛋白修饰谱的贝叶斯数据融合以推断基因调控网络。

数十年来,从高通量基因表达数据中正确重建基因调控网络(GRN)一直是系统生物学的主要挑战。已经提出了许多解决该问题的方法。但是,GRN推断仍有很大的改进空间。整合来自不同来源的数据是一种很有前途的策略。表观遗传修饰与基因调控密切相关。因此,表观遗传数据(例如组蛋白修饰图谱)可以为揭示基因之间的调控相互作用提供有用的信息。在本文中,我们提出了一种将表观遗传数据整合到GRN推理中的方法。特别地,采用动态贝叶斯网络(DBN)从时序基因表达数据推断基因调控。表观遗传数据(此处为组蛋白修饰谱)被整合到贝叶斯模型的先验概率分布中。我们的方法已在合成数据集和真实数据集上得到验证。实验结果表明,表观遗传数据的整合可以显着提高GRN推理的性能。随着更多表观遗传数据集的获得,我们的方法将有助于阐明驱动各种细胞活动的基因调控机制。源代码和测试数据集位于https://github.com/Zheng-Lab/MetaGRN/tree/master/histonePrior。随着更多表观遗传数据集的获得,我们的方法将有助于阐明驱动各种细胞活动的基因调控机制。源代码和测试数据集位于https://github.com/Zheng-Lab/MetaGRN/tree/master/histonePrior。随着更多表观遗传数据集的获得,我们的方法将有助于阐明驱动各种细胞活动的基因调控机制。源代码和测试数据集位于https://github.com/Zheng-Lab/MetaGRN/tree/master/histonePrior。
更新日期:2020-04-22
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