TVAE-RNA: ensemble-based RNA secondary structure prediction via transformer variational autoencoders.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 40981507.
- Also identified by DOI 10.1093/bioinformatics/btaf527 and PMC identifier 12640237.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Accurate prediction of RNA secondary structure remains challenging due to the presence of pseudoknots, long-range dependencies, and limited labeled data. 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. 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.
Medical subject headings
- RNA
- Nucleic Acid Conformation
- Software
- Sequence Analysis, RNA
- Computational Biology