Abstract

BackgroundSmall interfering RNA (siRNA) can be used to post-transcriptional gene regulation by knocking down targeted genes. In functional genomics, biomedical research and cancer therapeutics, siRNA design is a critical research topic. Various computational algorithms have been developed to select the most effective siRNA, whereas the efficacy prediction accuracy is not so satisfactory. Many existing computational methods are based on feature engineering, which may lead to biased and incomplete features. Deep learning utilizes non-linear mapping operations to detect potential feature pattern and has been considered perform better than existing machine learning method.ResultsIn this paper, to further improve the prediction accuracy and facilitate gene functional studies, we developed a new powerful siRNA efficacy predictor based on a deep architecture. First, we extracted hidden feature patterns from two modalities, including sequence context features and thermodynamic property. Then, we constructed a deep architecture to implement the prediction. On the available largest siRNA database, the performance of our proposed method was measured with 0.725 PCC and 0.903 AUC value. The comparative experiment showed that our proposed architecture outperformed several siRNA prediction methods.ConclusionsThe results demonstrate that our deep architecture is stable and efficient to predict siRNA silencing efficacy. The method could help select candidate siRNA for targeted mRNA, and further promote the development of RNA interference.

Highlights

  • Small interfering RNA can be used to post-transcriptional gene regulation by knocking down targeted genes

  • RNA interference (RNAi) is a vital tool for researching gene function [5,6,7] and can be used as an effective therapeutic method in the treatment of virus and cancer [8,9,10]

  • The gene silencing efficacy of RNAi relies on Small interfering RNA (siRNA) design, and many efforts are being made in this area

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Summary

Introduction

Small interfering RNA (siRNA) can be used to post-transcriptional gene regulation by knocking down targeted genes. Small interfering RNA (siRNA) is the production of RNAi, which can induce instant target gene knockdown [3]. Han et al BMC Genomics 2018, 19(Suppl 7):669 prediction methods [18] As another artificial neural network, ThermoComposition-21 [19] includes both composition and thermodynamic features. One is the nucleotides present at each position in the siRNA sequence, the other is the global content of the siRNA in short motifs It is an accurate and interpretable model, and according the experimental results the prediction accuracy of Biopredsi is as accurate as it. Another linear regression model was constructed by nucleotide preference scores [21]

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