GenVarLoader: an accelerated dataloader for applying deep learning to personalized genomics
Abstract Background Deep learning models can predict the functional impact of genetic variants. However, training and applying these sequence models to personalized genome sequences are severely constrained by the computational burden of storing and reading massive datasets. Results We developed GenVarLoader, an accelerated dataloader that creates personalized genomic sequences and functional tracks on-the-fly to overcome these bottlenecks. GenVarLoader stores this personalized genomic data in formats specifically optimized for machine learning. Our tool reads variants up to 26,000 times faster than a pre-subset BCF, loads personalized data up to 130 times faster than tuned FASTA and pyBigWig pipelines, and reduces storage approximately 2,000-fold compared to existing alternatives. Conclusions By eliminating severe data loading bottlenecks, GenVarLoader ensures efficient model training and inference. It provides a scalable solution for integrating biobank-scale personalized genomic data with deep learning applications.
Authors
- David Laub (ORCID: https://orcid.org/0000-0001-5912-6458)
- Rany M. Salem (ORCID: https://orcid.org/0000-0001-8816-6862)
- A. Ho (ORCID: https://orcid.org/0000-0001-5107-3531)
- Graham McVicker (ORCID: https://orcid.org/0000-0003-0991-0951)
- Hannah Carter (ORCID: https://orcid.org/0000-0002-1729-2463)
- Loukik Raina
- Adam Klie
- Jeff Jaureguy
Institutions
- Salk Institute for Biological Studies (US)
- University of California San Diego (US)
- Human Longevity (United States) (US)
Publication Details
- Journal
- BMC Genomics
- Published
- 2026-07-24
- DOI
- https://doi.org/10.1186/s12864-026-13225-5
- Citations
- 2
- Primary Topic
- Gene expression and cancer classification
- Type
- article
- Field-Weighted Citation Impact
- 8.09
Funders
- National Institutes of Health
- National Human Genome Research Institute
- U.S. National Library of Medicine