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多网络逻辑矩阵分解在代谢物-疾病相互作用预测中的应用。

Multi-network logistic matrix factorization for metabolite-disease interaction prediction.

机构信息

School of Computer, Central China Normal University, Wuhan, China.

School of Mathematics & Statistics, Central China Normal University, Wuhan, China.

出版信息

FEBS Lett. 2020 Jun;594(11):1675-1684. doi: 10.1002/1873-3468.13782. Epub 2020 Apr 26.

Abstract

Identifying disease-related metabolites is of great significance for the diagnosis, prevention, and treatment of disease. In this study, we propose a novel computational model of multiple-network logistic matrix factorization (MN-LMF) for predicting metabolite-disease interactions, which is especially relevant for new diseases and new metabolites. First, MN-LMF builds disease (or metabolite) similarity network by integrating heterogeneous omics data. Second, it combines these similarities with known metabolite-disease interaction networks, using modified logistic matrix factorization to predict potential metabolite-disease interactions. Experimental results show that MN-LMF accurately predicts metabolite-disease interactions, and outperforms other state-of-the-art methods. Moreover, case studies also demonstrated the effectiveness of the model to infer unknown metabolite-disease interactions for novel diseases without any known associations.

摘要

鉴定与疾病相关的代谢物对于疾病的诊断、预防和治疗具有重要意义。在本研究中,我们提出了一种新的基于多网络逻辑矩阵分解(MN-LMF)的计算模型,用于预测代谢物-疾病相互作用,这对于新疾病和新代谢物尤为相关。首先,MN-LMF 通过整合异构组学数据构建疾病(或代谢物)相似性网络。其次,它将这些相似性与已知的代谢物-疾病相互作用网络相结合,使用改进的逻辑矩阵分解来预测潜在的代谢物-疾病相互作用。实验结果表明,MN-LMF 能够准确预测代谢物-疾病相互作用,并且优于其他最先进的方法。此外,案例研究还证明了该模型对于推断新型疾病中没有任何已知关联的未知代谢物-疾病相互作用的有效性。

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