GTFKAN: A Novel Microbe-drug Association Prediction Model Based on Graph Transformer and Fourier Kolmogorov-Arnold Networks

IF 4.7 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Jiacheng Lai, Zhen Zhang, Bin Zeng, Lei Wang
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引用次数: 0

Abstract

Microbes have been shown to be closely related to human health. In recent years, lots of computational methods for predicting microbial-drug association have been proposed. In this manuscript, we introduced a novel predictive model, called GTFKAN, to identify potential microbe-drug associations by combining Graph Transformation Networks (GTN) with Fourier Kolmogorov-Arnold Networks (FKAN). In GTFKAN, we would first compute the Gaussian kernel and functional similarity of microbes and drugs respectively, and then adopt random walk and restart (RWR) methods to enhance these similar features to construct a new microbe-drug heterogeneous network HN. At the same time, we would further calculate the cosine similarity of microbes and diseases to construct another microbe-drug heterogeneous network LDIM. Next, we would input HN into GTN to derive the location and structural features of microorganisms and drugs, and input LDIM into FKAN to extract the hidden higher-order features of microorganisms and drugs, respectively. Finally, we would integrate these two features extracted by GTN and FKAN and feed the integrated features into the MLP classifier to infer potential microbial-drug associations. Moreover, to evaluate the performance of GTFKAN, we compared it with state-of-the-art methods based on well-known public datasets, and the experimental results show that GTFKAN can achieve satisfactory predictive performance. In addition, the results of ablation experiments and case studies also demonstrated the superiority of GTFKAN, which means that GTFKAN may be a useful microbial-drug association prediction tool in the future.
GTFKAN:一种基于图变换和傅里叶Kolmogorov-Arnold网络的微生物-药物关联预测模型。
微生物已被证明与人类健康密切相关。近年来,人们提出了许多预测微生物-药物关联的计算方法。在这篇论文中,我们引入了一种新的预测模型,称为GTFKAN,通过结合图变换网络(GTN)和傅立叶Kolmogorov-Arnold网络(FKAN)来识别潜在的微生物-药物关联。在GTFKAN中,我们首先分别计算微生物和药物的高斯核和功能相似度,然后采用随机漫步和重启(RWR)方法增强这些相似特征,构建新的微生物-药物异质网络HN。同时,我们将进一步计算微生物和疾病的余弦相似度,构建另一个微生物-药物异质网络LDIM。接下来,我们将HN输入到GTN中,推导出微生物和药物的位置和结构特征,将LDIM输入到FKAN中,分别提取出微生物和药物隐藏的高阶特征。最后,我们将整合GTN和FKAN提取的这两个特征,并将整合的特征输入到MLP分类器中,以推断潜在的微生物-药物关联。此外,为了评估GTFKAN的性能,我们将其与基于知名公共数据集的最新方法进行了比较,实验结果表明GTFKAN可以获得令人满意的预测性能。此外,消融实验和病例研究的结果也证明了GTFKAN的优越性,这意味着GTFKAN在未来可能是一种有用的微生物-药物关联预测工具。
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来源期刊
Journal of Molecular Biology
Journal of Molecular Biology 生物-生化与分子生物学
CiteScore
11.30
自引率
1.80%
发文量
412
审稿时长
28 days
期刊介绍: Journal of Molecular Biology (JMB) provides high quality, comprehensive and broad coverage in all areas of molecular biology. The journal publishes original scientific research papers that provide mechanistic and functional insights and report a significant advance to the field. The journal encourages the submission of multidisciplinary studies that use complementary experimental and computational approaches to address challenging biological questions. Research areas include but are not limited to: Biomolecular interactions, signaling networks, systems biology; Cell cycle, cell growth, cell differentiation; Cell death, autophagy; Cell signaling and regulation; Chemical biology; Computational biology, in combination with experimental studies; DNA replication, repair, and recombination; Development, regenerative biology, mechanistic and functional studies of stem cells; Epigenetics, chromatin structure and function; Gene expression; Membrane processes, cell surface proteins and cell-cell interactions; Methodological advances, both experimental and theoretical, including databases; Microbiology, virology, and interactions with the host or environment; Microbiota mechanistic and functional studies; Nuclear organization; Post-translational modifications, proteomics; Processing and function of biologically important macromolecules and complexes; Molecular basis of disease; RNA processing, structure and functions of non-coding RNAs, transcription; Sorting, spatiotemporal organization, trafficking; Structural biology; Synthetic biology; Translation, protein folding, chaperones, protein degradation and quality control.
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