| Literature DB >> 29763707 |
Guanghui Li1, Jiawei Luo2, Qiu Xiao2, Cheng Liang3, Pingjian Ding2.
Abstract
Interactions between microRNAs (miRNAs) and diseases can yield important information for uncovering novel prognostic markers. Since experimental determination of disease-miRNA associations is time-consuming and costly, attention has been given to designing efficient and robust computational techniques for identifying undiscovered interactions. In this study, we present a label propagation model with linear neighborhood similarity, called LPLNS, to predict unobserved miRNA-disease associations. Additionally, a preprocessing step is performed to derive new interaction likelihood profiles that will contribute to the prediction since new miRNAs and diseases lack known associations. Our results demonstrate that the LPLNS model based on the known disease-miRNA associations could achieve impressive performance with an AUC of 0.9034. Furthermore, we observed that the LPLNS model based on new interaction likelihood profiles could improve the performance to an AUC of 0.9127. This was better than other comparable methods. In addition, case studies also demonstrated our method's outstanding performance for inferring undiscovered interactions between miRNAs and diseases, especially for novel diseases.Keywords: Disease-related miRNAs; Label propagation; Linear neighborhood similarity; miRNA-disease association
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Year: 2018 PMID: 29763707 DOI: 10.1016/j.jbi.2018.05.005
Source DB: PubMed Journal: J Biomed Inform ISSN: 1532-0464 Impact factor: 6.317