Predicting disease genes based on multi-head attention fusion

被引:3
|
作者
Zhang, Linlin [1 ]
Lu, Dianrong [2 ]
Bi, Xuehua [3 ]
Zhao, Kai [2 ]
Yu, Guanglei [3 ]
Quan, Na [2 ]
机构
[1] Xinjiang Univ, Coll Software Engn, Urumqi, Peoples R China
[2] Xinjiang Univ, Coll informat Sci & Engn, Urumqi, Peoples R China
[3] Xinjiang Med Univ, Med Engn & Technol Coll, Urumqi, Peoples R China
关键词
Pathogenic gene prediction; Heterogeneous network; Multi-head attention; Graph representation learning; GENOME-WIDE ASSOCIATION; HETEROGENEOUS NETWORKS; PRIORITIZATION; INTEGRATION; CANCER;
D O I
10.1186/s12859-023-05285-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
BackgroundThe identification of disease-related genes is of great significance for the diagnosis and treatment of human disease. Most studies have focused on developing efficient and accurate computational methods to predict disease-causing genes. Due to the sparsity and complexity of biomedical data, it is still a challenge to develop an effective multi-feature fusion model to identify disease genes.ResultsThis paper proposes an approach to predict the pathogenic gene based on multi-head attention fusion (MHAGP). Firstly, the heterogeneous biological information networks of disease genes are constructed by integrating multiple biomedical knowledge databases. Secondly, two graph representation learning algorithms are used to capture the feature vectors of gene-disease pairs from the network, and the features are fused by introducing multi-head attention. Finally, multi-layer perceptron model is used to predict the gene-disease association.ConclusionsThe MHAGP model outperforms all of other methods in comparative experiments. Case studies also show that MHAGP is able to predict genes potentially associated with diseases. In the future, more biological entity association data, such as gene-drug, disease phenotype-gene ontology and so on, can be added to expand the information in heterogeneous biological networks and achieve more accurate predictions. In addition, MHAGP with strong expansibility can be used for potential tasks such as gene-drug association and drug-disease association prediction.
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页数:15
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