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ABSTRACT: Motivation
Accurate prediction of RNA secondary structure remains challenging due to the presence of pseudoknots, long-range dependencies, and limited labeled data.Results
We propose TVAE, a novel framework that integrates a Transformer encoder with a Variational Autoencoder (VAE). The Transformer captures global dependencies in the sequence, while the VAE models structural variability by learning a probabilistic latent space. Unlike deterministic models, TVAE generates diverse and biologically plausible secondary structures, enabling more comprehensive structure discovery. To obtain discrete predictions, we introduce GHA-Pairing, a fast and biologically constrained base-pairing algorithm. TVAE demonstrates strong generalization across different RNA families and achieves state-of-the-art performance on benchmark datasets, reaching an F1 score of 0.89 and 83% accuracy, surpassing existing methods by 10%. These results highlight the advantage of probabilistic modeling for RNA structure prediction and its potential to enhance biological insights.Availability and implementation
Code and pretrained models are available at https://github.com/mei-rna/TVAE-RNA. The released version of the dataset and models can also be accessed via DOI: 10.5281/zenodo.16946114.
SUBMITTER: Mei X
PROVIDER: S-EPMC12640237 | biostudies-literature | 2025 Nov
REPOSITORIES: biostudies-literature

Bioinformatics (Oxford, England) 20251101 11
<h4>Motivation</h4>Accurate prediction of RNA secondary structure remains challenging due to the presence of pseudoknots, long-range dependencies, and limited labeled data.<h4>Results</h4>We propose TVAE, a novel framework that integrates a Transformer encoder with a Variational Autoencoder (VAE). The Transformer captures global dependencies in the sequence, while the VAE models structural variability by learning a probabilistic latent space. Unlike deterministic models, TVAE generates diverse a ...[more]