BMC Bioinformatics (Nov 2021)

SVDNVLDA: predicting lncRNA-disease associations by Singular Value Decomposition and node2vec

  • Jianwei Li,
  • Jianing Li,
  • Mengfan Kong,
  • Duanyang Wang,
  • Kun Fu,
  • Jiangcheng Shi

DOI
https://doi.org/10.1186/s12859-021-04457-1
Journal volume & issue
Vol. 22, no. 1
pp. 1 – 18

Abstract

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Abstract Background Numerous studies on discovering the roles of long non-coding RNAs (lncRNAs) in the occurrence, development and prognosis progresses of various human diseases have drawn substantial attentions. Since only a tiny portion of lncRNA-disease associations have been properly annotated, an increasing number of computational methods have been proposed for predicting potential lncRNA-disease associations. However, traditional predicting models lack the ability to precisely extract features of biomolecules, it is urgent to find a model which can identify potential lncRNA-disease associations with both efficiency and accuracy. Results In this study, we proposed a novel model, SVDNVLDA, which gained the linear and non-linear features of lncRNAs and diseases with Singular Value Decomposition (SVD) and node2vec methods respectively. The integrated features were constructed from connecting the linear and non-linear features of each entity, which could effectively enhance the semantics contained in ultimate representations. And an XGBoost classifier was employed for identifying potential lncRNA-disease associations eventually. Conclusions We propose a novel model to predict lncRNA-disease associations. This model is expected to identify potential relationships between lncRNAs and diseases and further explore the disease mechanisms at the lncRNA molecular level.

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