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• W2969761002 abstract "Long non-coding RNA (lncRNA) play critical roles in the occurrence and development of various diseases. The determination of the lncRNA-disease associations thus would contribute to provide new insights into the pathogenesis of the disease, the diagnosis, and the gene treatments. Considering that traditional experimental approaches are difficult to detect potential human lncRNA-disease associations from the vast amount of biological data, developing computational method could be of significant value. In this paper, we proposed a novel computational method named LDASR to identify associations between lncRNA and disease by analyzing known lncRNA-disease associations. First, the feature vectors of the lncRNA-disease pairs were obtained by integrating lncRNA Gaussian interaction profile kernel similarity, disease semantic similarity, and Gaussian interaction profile kernel similarity. Second, autoencoder neural network was employed to reduce the feature dimension and get the optimal feature subspace from the original feature set. Finally, Rotating Forest was used to carry out prediction of lncRNA-disease association. The proposed method achieves an excellent preference with 0.9502 AUC in leave-one-out cross-validations (LOOCV) and 0.9428 AUC in 5-fold cross-validation, which significantly outperformed previous methods. Moreover, two kinds of case studies on identifying lncRNAs associated with colorectal cancer and glioma further proves the capability of LDASR in identifying novel lncRNA-disease associations. The promising experimental results show that the LDASR can be an excellent addition to the biomedical research in the future." @default.
• W2969761002 created "2019-08-29" @default.
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• W2969761002 date "2019-09-01" @default.
• W2969761002 modified "2023-10-16" @default.
• W2969761002 title "A Learning-Based Method for LncRNA-Disease Association Identification Combing Similarity Information and Rotation Forest" @default.
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• W2969761002 doi "https://doi.org/10.1016/j.isci.2019.08.030" @default.
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