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MGCNSS: miRNA-disease association prediction with multi-layer graph convolution and distance-based negative sample selection strategy.
Tian, Zhen; Han, Chenguang; Xu, Lewen; Teng, Zhixia; Song, Wei.
Affiliation
  • Tian Z; School of Computer and Artificial Intelligence, Zhengzhou University, Zhengzhou 450000, China.
  • Han C; Yangtze Delta Region Institute (Quzhou), University of Electronic Science and Technology of China, Quzhou 324000, China.
  • Xu L; School of Computer and Artificial Intelligence, Zhengzhou University, Zhengzhou 450000, China.
  • Teng Z; School of Computer and Artificial Intelligence, Zhengzhou University, Zhengzhou 450000, China.
  • Song W; College of Computer and Control Engineering, Northeast Forestry University, Harbin 150040, China.
Brief Bioinform ; 25(3)2024 Mar 27.
Article in En | MEDLINE | ID: mdl-38622356
ABSTRACT
Identifying disease-associated microRNAs (miRNAs) could help understand the deep mechanism of diseases, which promotes the development of new medicine. Recently, network-based approaches have been widely proposed for inferring the potential associations between miRNAs and diseases. However, these approaches ignore the importance of different relations in meta-paths when learning the embeddings of miRNAs and diseases. Besides, they pay little attention to screening out reliable negative samples which is crucial for improving the prediction accuracy. In this study, we propose a novel approach named MGCNSS with the multi-layer graph convolution and high-quality negative sample selection strategy. Specifically, MGCNSS first constructs a comprehensive heterogeneous network by integrating miRNA and disease similarity networks coupled with their known association relationships. Then, we employ the multi-layer graph convolution to automatically capture the meta-path relations with different lengths in the heterogeneous network and learn the discriminative representations of miRNAs and diseases. After that, MGCNSS establishes a highly reliable negative sample set from the unlabeled sample set with the negative distance-based sample selection strategy. Finally, we train MGCNSS under an unsupervised learning manner and predict the potential associations between miRNAs and diseases. The experimental results fully demonstrate that MGCNSS outperforms all baseline methods on both balanced and imbalanced datasets. More importantly, we conduct case studies on colon neoplasms and esophageal neoplasms, further confirming the ability of MGCNSS to detect potential candidate miRNAs. The source code is publicly available on GitHub https//github.com/15136943622/MGCNSS/tree/master.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Colonic Neoplasms / MicroRNAs Limits: Humans Language: En Journal: Brief Bioinform Journal subject: BIOLOGIA / INFORMATICA MEDICA Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Colonic Neoplasms / MicroRNAs Limits: Humans Language: En Journal: Brief Bioinform Journal subject: BIOLOGIA / INFORMATICA MEDICA Year: 2024 Document type: Article Affiliation country:
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