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A Fast Linear Neighborhood Similarity-Based Network Link Inference Method to Predict MicroRNA-Disease Associations
Abstract:
Increasing evidences revealed that microRNAs (miRNAs) play critical roles in important biological processes. The identification of disease-related miRNAs is critical to understand the molecular mechanisms of human diseases. Most existing computational methods require diverse features to predict miRNA-disease associations. However, diverse features are not available for all miRNAs or diseases. In addition, most methods can't predict links for miRNAs or diseases without association information. In this paper, we propose a fast linear neighborhood similarity-based network link inference method, named FLNSNLI, to predict miRNA-disease associations. First, known miRNA-disease associations are formulated as a bipartite network, and miRNAs (or diseases) are expressed as association profiles. Second, miRNA-miRNA similarity and disease-disease similarity are calculated by fast linear neighborhood similarity measure and association profiles. Third, the label propagation algorithm is respectively implemented on two sides to score candidate miRNA-disease associations. Finally, FLNSNLI adopts the weighted average strategy and makes predictions. Moreover, we develop a link complementing approach, and extend FLNSNLI to predict links for miRNAs (or diseases) without known associations. In computational experiments, FLNSNLI produces high-accuracy performances, and outperforms other state-of-the-art methods. More importantly, FLNSNLI requires less information but performs well. Case studies on three popular diseases show that FLNSNLI is useful for the microRNA-disease association prediction.
Insights
This study introduces FLNSNLI, a novel computational method for predicting microRNA-disease associations. FLNSNLI accurately identifies links using limited data and can predict associations for previously unlinked microRNAs and diseases.
Area of Science:
- Genomics
- Bioinformatics
- Computational Biology
Background:
- MicroRNAs (miRNAs) are crucial regulators of biological processes, and identifying disease-associated miRNAs is key to understanding human diseases.
- Current computational methods for miRNA-disease association prediction often require extensive features, limiting their applicability and failing to predict links for novel or unassociated entities.
Purpose of the Study:
- To develop a fast and accurate computational method for predicting miRNA-disease associations.
- To address the limitations of existing methods by requiring less information and enabling predictions for entities without prior association data.
Main Methods:
- Formulated known miRNA-disease associations as a bipartite network and represented miRNAs/diseases using association profiles.
- Calculated miRNA-miRNA and disease-disease similarity using a fast linear neighborhood similarity measure.
- Employed label propagation and a weighted average strategy for prediction, with a link complementing approach to extend predictions.
Main Results:
- FLNSNLI demonstrated high-accuracy performance in computational experiments.
- The method outperformed existing state-of-the-art approaches.
- FLNSNLI proved effective even with limited input information.
Conclusions:
- FLNSNLI offers a robust and efficient solution for predicting miRNA-disease associations.
- The method's ability to predict links for unassociated entities enhances its utility in biological research.
- Case studies confirmed FLNSNLI's practical value in identifying disease-related microRNAs.
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