BACKGROUND: RNA 5-methyluridine (m5U) modifications play a crucial role in biological processes, making their accurate identification a key focus in computational biology. This paper introduces Deep-m5U, a robust predictor designed to enhance the prediction of m5U modifications. The proposed method, named Deep-m5U, utilizes a hybrid pseudo-K-tuple nucleotide composition (PseKNC) for sequence formulation, a Shapley Additive exPlanations (SHAP) algorithm for discriminant feature selection, and a deep neural network (DNN) as the classifier. RESULTS: The model was evaluated using two benchmark datasets, i.e., Full Transcript and Mature mRNA. Deep-m5U achieved overall accuracies of 91.47% and 95.86% for the Full Transcript and Mature mRNA datasets with 10-fold cross-validation, and for independent samples, the model attained 92.94% and 95.17% accuracy. CONCLUSION: Compared to existing models, Deep-m5U showed approximately 5.23% and 3.73% higher accuracy on the training data and 3.95% and 3.26% higher accuracy on independent samples for the Full Transcript and Mature mRNA datasets, respectively. The reliability and effectiveness of Deep-m5U make it a valuable tool for scientists and a potential asset in pharmaceutical design and research.
No takes yet. Share an insight, caveat, or question.
Noor et al. (2024) studied this question.
Synapse has enriched one closely related paper. Consider it for comparative context: