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Prediction of potential drug-microbe associations based on matrix factorization and a three-layer heterogeneous network.
Li, Han; Hou, Zhen-Jie; Zhang, Wen-Guang; Qu, Jia; Yao, Hai-Bin; Chen, Yan.
Afiliação
  • Li H; School of Computer Science and Artificial Intelligence, Changzhou University, Changzhou 213164, China.
  • Hou ZJ; School of Computer Science and Artificial Intelligence, Changzhou University, Changzhou 213164, China. Electronic address: hhderek@163.com.
  • Zhang WG; School of Life Sciences, Inner Mongolia Agricultural University, Hohhot 010000, China.
  • Qu J; School of Computer Science and Artificial Intelligence, Changzhou University, Changzhou 213164, China.
  • Yao HB; School of Computer Science and Artificial Intelligence, Changzhou University, Changzhou 213164, China.
  • Chen Y; School of Computer Science and Artificial Intelligence, Changzhou University, Changzhou 213164, China.
Comput Biol Chem ; 104: 107857, 2023 Jun.
Article em En | MEDLINE | ID: mdl-37018909
ABSTRACT
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Algoritmos / Biologia Computacional Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Comput Biol Chem Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Algoritmos / Biologia Computacional Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Comput Biol Chem Ano de publicação: 2023 Tipo de documento: Article