4.7 Article

A novel graph attention model for predicting frequencies of drug-side effects from multi-view data

期刊

BRIEFINGS IN BIOINFORMATICS
卷 22, 期 6, 页码 -

出版社

OXFORD UNIV PRESS
DOI: 10.1093/bib/bbab239

关键词

drug-side effect frequencies; deep learning; multi-view data

资金

  1. NSFC-Zhejiang Joint Fund for the Integration of Industrialization and Informatization [U1909208]
  2. National Natural Science Foundation of China [61772552, 61832019]
  3. 111 Project [B18059]
  4. Hunan Provincial Science and Technology Program [2018WK4001]
  5. Scientific Research Fund of Hunan Provincial Education Department [18B469]

向作者/读者索取更多资源

Identifying the frequencies of drug side effects is crucial in pharmacology, but designing clinical trials for this purpose can be time-consuming and costly. This study proposes a novel prediction model that integrates different types of features using a graph neural network, outperforming existing methods in effectiveness and accuracy.
Identifying the frequencies of the drug-side effects is a very important issue in pharmacological studies and drug risk-benefit. However, designing clinical trials to determine the frequencies is usually time consuming and expensive, and most existing methods can only predict the drug-side effect existence or associations, not their frequencies. Inspired by the recent progress of graph neural networks in the recommended system, we develop a novel prediction model for drug-side effect frequencies, using a graph attention network to integrate three different types of features, including the similarity information, known drug-side effect frequency information and word embeddings. In comparison, the few available studies focusing on frequency prediction use only the known drug-side effect frequency scores. One novel approach used in this work first decomposes the feature types in drug-side effect graph to extract different view representation vectors based on three different type features, and then recombines these latent view vectors automatically to obtain unified embeddings for prediction. The proposed method demonstrates high effectiveness in 10-fold cross-validation. The computational results show that the proposed method achieves the best performance in the benchmark dataset, outperforming the state-of-the-art matrix decomposition model. In addition, some ablation experiments and visual analyses are also supplied to illustrate the usefulness of our method for the prediction of the drug-side effect frequencies. The codes of MGPred are available at https://github.com/zhc940702/MGPred and https://zenodo.org/record/4449613.

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