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Updated: Jun 23, 2026

Identification of Alternative Splicing and Polyadenylation in RNA-seq Data
Published on: June 24, 2021
SpliceSelectNet: a hierarchical Transformer-based deep learning model for splice site prediction
Yuna Miyachi1, Kenta Nakai1,2
1Department of Computer Science, Graduate School of Information Science and Technology, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, 113-8656 Tokyo, Japan.
Abstract:
Accurate RNA splicing is essential for gene expression and protein function, yet the mechanisms governing splice site recognition remain incompletely understood. Aberrant splicing caused by mutations can lead to severe diseases, including cancer and genetic disorders, underscoring the need for accurate computational tools to predict splice sites and detect disruptions. Existing methods have made significant advances in splice site prediction but are often limited in handling long-range dependencies due to high computational costs, a factor critical to splicing regulation. Moreover, many models lack interpretability, hindering efforts to elucidate the underlying biological mechanisms. Here, we present SpliceSelectNet (SSNet), a hierarchical Transformer-based deep learning model that predicts splice sites from DNA sequences spanning up to 100 kb. By integrating local and global attention mechanisms, SSNet efficiently captures both proximal and distal regulatory signals while maintaining single-nucleotide resolution. Across multiple benchmark datasets, SSNet achieves state-of-the-art performance in splice site prediction and aberrant splicing detection. Systematic in silico mutagenesis demonstrates that attention scores reflect functional sequence importance, supporting their biological relevance. Long-range sequence perturbation experiments further show that SSNet captures distal regulatory effects beyond conventional receptive fields. Together, these results establish SSNet as a biologically interpretable framework for modeling long-range splicing regulation from genomic sequence.
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