Evidence map›Paper›PMID 40981507›Full record

ArticleBioinformatics (Oxford, England)2025

TVAE-RNA: ensemble-based RNA secondary structure prediction via transformer variational autoencoders.

Xiyuan Mei, Hanbo Liu, Yuheng Zhu, Enshuang Zhao, Longyi Li, Hao Zhang

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Article in Bioinformatics (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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6 authors.

Xiyuan MeiCollege of Computer Science and Technology, Jilin University, Changchun 130012, China.ORCID 0009-0000-9487-5630
Hanbo LiuCollege of Computer Science and Technology, Jilin University, Changchun 130012, China.
Yuheng ZhuCollege of Computer Science and Technology, Jilin University, Changchun 130012, China.
Enshuang ZhaoCollege of Computer Science and Technology, Jilin University, Changchun 130012, China.
Longyi LiCollege of Computer Science and Technology, Jilin University, Changchun 130012, China.ORCID 0009-0002-6572-3544
Hao ZhangCollege of Computer Science and Technology, Jilin University, Changchun 130012, China.ORCID 0000-0002-2058-7123

Funding

National Natural Science Foundation of China 62072210
6 · The paper itself

Abstract

motivationAccurate prediction of RNA secondary structure remains challenging due to the presence of pseudoknots, long-range dependencies, and limited labeled data.

resultsWe 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.

Indexed as

Computational BiologyNucleic Acid ConformationRNASequence Analysis, RNASoftwareAlgorithmsAutoencoderBase PairingRNA

Identifiers

PMID40981507
PMCPMC12640237

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.