Authors
Bellido Molias, F., Kudla, G.
Abstract
Computational predictors of RNA splicing are increasingly used to interpret genetic variants and to design synthetic genes, yet they are almost always benchmarked on endogenous human sequences closely related to their training data. Whether their performance reflects genuine recognition of splicing signals, or instead exploits statistical features of natural genomes such as conservation and exon-intron composition, remains unclear. Here we benchmark eleven splicing predictors on thousands of synthetic GFP variants that are heavily recoded and dissimilar from any training data, using long-read sequencing to measure splicing directly at each position. Despite this distribution shift, modern deep-learning predictors retained strong performance, and the resulting ranking was largely stable across position-level and construct-level benchmarks. SpliceTransformer ranked highest, followed by AlphaGenome and SpliceAI. Tools that ignore long-range sequence context performed substantially worse, largely because they assign high scores to many non-spliced positions. This ranking broadly agrees with benchmarks on endogenous variants, indicating that the leading models capture transferable, sequence-intrinsic determinants of splicing. We further provide a unified calibration that maps each predictor's scores onto the measured fraction of spliced reads, allowing scores to be interpreted as splicing outcomes and compared directly between tools. Our results show that current deep-learning models generalise beyond natural genomes and provide a practical framework for splicing-aware sequence design.
Preprint server:
bioRxiv
The authors list and abstract were imported from bioRxiv on 28 Aug 2026.
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