Sequence modeling and design from molecular to genome scale with Evo

Author:

Nguyen Eric,Poli Michael,Durrant Matthew G,Thomas Armin W,Kang Brian,Sullivan Jeremy,Ng Madelena Y,Lewis Ashley,Patel Aman,Lou Aaron,Ermon Stefano,Baccus Stephen A,Hernandez-Boussard Tina,Re Christopher,Hsu Patrick D,Hie Brian LORCID

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.

Publisher

Cold Spring Harbor Laboratory

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