Variant-resolved prediction of context-specific isoform variation with a graph-based attention model
Abstract
In eukaryotes, most genes produce multiple transcript isoforms that diversify the transcriptome and proteome, serving as a key mechanism of functional regulation. Genetic variation can disrupt the RNA processing signals that shape isoform structure and abundance, yet modeling these effects at full-length isoform resolution remains challenging due to the complexity of transcript regulation. Here, we introduce Otari, an attention-based graph neural network framework trained on the human genomic sequence and long-read transcriptomes across 30 tissue types and brain regions. Otari predicts tissue-specific differential isoform abundance by integrating sequence-derived epigenetic and post-transcriptional signals, enabling isoform-resolved variant effect interpretation. Applied to large-scale variant datasets, including an autism cohort, Otari uncovers patterns of isoform dysregulation undetectable at the gene level, such as variant-driven perturbations in isoform abundance and microexon usage implicated in autism pathophysiology. We provide Otari as a resource for powering isoform-level analyses across tissues at scale.
Fields of Study & Subjects
Genomics and Chromatin Dynamics
Genomics and Rare Diseases
Genomic variations and chromosomal abnormalities
Publication details
- Journal / source
- Cell Genomics
- Publisher
- Elsevier BV
- Volume
- 6
- Issue
- 4
- Pages
- 101126–101126
- Publication date
- 16 January 2026
- Language
- EN