A Novel Topology-Based Candidate Reaction Prediction Approach for Gap-Fillings of Genome-Scale Metabolic Models

一种基于拓扑结构的新型候选反应预测方法,用于填补基因组规模代谢模型中的空白

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Abstract

Background: It is significant to predict and fill metabolic reaction gaps (gap-fillings) for reconstructions of high-quality genome-scale metabolic models (GEMs). Currently, many existing optimization-based gap-filling methods have to rely on phenotypic data, while performances of topology-based approaches by deep learning algorithms need to be further improved. Methods: This paper proposes a novel topology-based approach (GHCN-SE) of predicting confidence scores of candidate reactions, which can be used for gap-fillings of GEMs. The topological features of GEMs are fully extracted by simultaneously using graph and hypergraph convolutional networks, such that both associations of metabolites in the same reaction and higher-order interactions of metabolites within reactions can be captured. After the feature fusion, we further employ the squeeze-and-excitation network to enhance features. Results: The reaction prediction and reaction recovery experiments through 5-fold cross validations on 108 high-quality BiGG GEMs show that the proposed GHCN-SE is superior to other related methods. The ablation study further demonstrates the contributions of the graph convolutional network, hypergraph convolutional network, and squeeze-and-excitation network in GHCN-SE. In addition, the visualization study interprets the effectiveness of GHCN-SE. Conclusions: For potential applications in metabolic engineering, biomedicine, etc., this proposed GHCN-SE can be used to further improve the phenotypic prediction accuracy of the draft GEM generated from automated reconstruction tools.

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