Sequence modeling and design from molecular to genome scale with Evo
Open accessPreprint — published as 10.1126/science.ado9336 · Paper page
Abstract
The genome is a sequence that completely encodes the DNA, RNA, and proteins that orchestrate the function of a whole organism. Advances in machine learning combined with massive datasets of whole genomes could enable a biological foundation model that accelerates the mechanistic understanding and generative design of complex molecular interactions. We report Evo, a genomic foundation model that enables prediction and generation tasks from the molecular to genome scale. Using an architecture based on advances in deep signal processing, we scale Evo to 7 billion parameters with a context length of 131 kilobases (kb) at single-nucleotide, byte resolution. Trained on whole prokaryotic genomes, Evo can generalize across the three fundamental modalities of the central dogma of molecular biology to perform zero-shot function prediction that is competitive with, or outperforms, leading domain-specific language models. Evo also excels at multi-element generation tasks, which we demonstrate by generating synthetic CRISPR-Cas molecular complexes and entire transposable systems for the first time. Using information learned over whole genomes, Evo can also predict gene essentiality at nucleotide resolution and can generate coding-rich sequences up to 650 kb in length, orders of magnitude longer than previous methods. Advances in multi-modal and multi-scale learning with Evo provides a promising path toward improving our understanding and control of biology across multiple levels of complexity.
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References 144 · Cited by 592
- Authors
- Nguyen, E., Poli, M., Durrant, M. G., Thomas, A. W., Kang, B., Sullivan, J., Ng, M. Y., Lewis, A., Patel, A., Lou, A., Ermon, S., Baccus, S. A., Hernandez-Boussard, T., Re, C., Hsu, P. D., & Hie, B. L.
- Affiliations
- Arc Research Institute (US)
- Stanford University (US)
- Chan Zuckerberg Biohub San Francisco (US)
- Stanford Medicine (US)
- Corresponding author
- Nguyen, Eric
- Poli, Michael
- Durrant, Matthew G
- Kang, Brian
- Hsu, Patrick D
- Hie, Brian L
- ORCID
- Venue
- Science
- Publisher
- openRxiv
- Published
- 2024-02-27
- Volume
- 386
- Issue
- 6723
- Pages
- eado9336-eado9336
- ISSN
- 0036-8075 (ISSN-L)
- PMC
- PMC12057570
- OpenAlex
- W4404349982
- Cited by
- 592
- References
- 144
- Citations by year
- 2026: 285 · 2025: 246 · 2024: 61
- FWCI
- 80.49
- Type
- journal article
- Language
- en
- Open access
- green
- doi.org
- Licence
- cc-by
- Locations
- Science (publishedVersion)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (UL1TR003142, UM1TR004921)
- National Institute of Biomedical Imaging and Bioengineering (U54EB020405)
- National Center for Advancing Translational Sciences
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Machine Learning in Bioinformatics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › CRISPR and Genetic Engineering
- Keywords
- genomic foundation models, long-context language models, prokaryotic genomes, phage genome, scaling laws, genome organization
- MeSH terms
- DNA, DNA Transposable Elements, Models, Genetic, Mutation, RNA, Mutagenesis, Genome, Viral, Genome, Bacterial, Genome, Archaeal, Genomics, High-Throughput Nucleotide Sequencing, CRISPR-Cas Systems
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