药品
计算机科学
药物开发
补语(音乐)
生物网络
交叉验证
非负矩阵分解
计算生物学
药物发现
矩阵分解
人工智能
生物信息学
生物
药理学
生物化学
特征向量
物理
量子力学
互补
基因
表型
作者
Han Li,Zhenjie Hou,Wenguang Zhang,Jia Qu,Hai-bin Yao,Yan Chen
标识
DOI:10.1016/j.compbiolchem.2023.107857
摘要
Microbes in the human body are closely linked to many complex human diseases and are emerging as new drug targets. These microbes play a crucial role in drug development and disease treatment. Traditional methods of biological experiments are not only time-consuming but also costly. Using computational methods to predict microbe-drug associations can effectively complement biological experiments. In this experiment, we constructed heterogeneity networks for drugs, microbes, and diseases using multiple biomedical data sources. Then, we developed a model with matrix factorization and a three-layer heterogeneous network (MFTLHNMDA) to predict potential drug-microbe associations. The probability of microbe-drug association was obtained by a global network-based update algorithm. Finally, the performance of MFTLHNMDA was evaluated in the framework of leave-one-out cross-validation (LOOCV) and 5-fold cross-validation (5-fold CV). The results showed that our model performed better than six state-of-the-art methods that had AUC of 0.9396 and 0.9385 + /- 0.0000, respectively. This case study further confirms the effectiveness of MFTLHNMDA in identifying potential drug-microbe associations and new drug-microbe associations.
科研通智能强力驱动
Strongly Powered by AbleSci AI