4.6 Article

Predicting potential miRNA-disease associations based on more reliable negative sample selection

期刊

BMC BIOINFORMATICS
卷 23, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12859-022-04978-3

关键词

miRNA-disease association predictions; Supervised learning; Negative sample selection

资金

  1. National Natural Science Foundation of China [61862026, 62062063]

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The study proposes a computational method called KR-NSSM for selecting more reliable negative samples for miRNA-disease association predictions. By integrating two semi-supervised algorithms, the method effectively screens out reliable negative samples from unlabelled data, improving prediction accuracy and obtaining confirmation in known miRNA-disease association prediction models. This method could be a useful tool in negative sample selection for biomedical research.
Background Increasing biomedical studies have shown that the dysfunction of miRNAs is closely related with many human diseases. Identifying disease-associated miRNAs would contribute to the understanding of pathological mechanisms of diseases. Supervised learning-based computational methods have continuously been developed for miRNA-disease association predictions. Negative samples of experimentally-validated uncorrelated miRNA-disease pairs are required for these approaches, while they are not available due to lack of biomedical research interest. Existing methods mainly choose negative samples from the unlabelled ones randomly. Therefore, the selection of more reliable negative samples is of great importance for these methods to achieve satisfactory prediction results. Results In this study, we propose a computational method termed as KR-NSSM which integrates two semi-supervised algorithms to select more reliable negative samples for miRNA-disease association predictions. Our method uses a refined K-means algorithm for preliminary screening of likely negative and positive miRNA-disease samples. A Rocchio classification-based method is applied for further screening to receive more reliable negative and positive samples. We implement ablation tests in KR-NSSM and find that the combination of the two selection procedures would obtain more reliable negative samples for miRNA-disease association predictions. Comprehensive experiments based on fivefold cross-validations demonstrate improvements in prediction accuracy on six classic classifiers and five known miRNA-disease association prediction models when using negative samples chose by our method than by previous negative sample selection strategies. Moreover, 469 out of 1123 selected positive miRNA-disease associations by our method are confirmed by existing databases. Conclusions Our experiments show that KR-NSSM can screen out more reliable negative samples from the unlabelled ones, which greatly improves the performance of supervised machine learning methods in miRNA-disease association predictions. We expect that KR-NSSM would be a useful tool in negative sample selection in biomedical research.

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