dnaHNet: A Scalable and Hierarchical Foundation Model for Genomic Sequence Learning
Arnav Shah, Junzhe Li, Parsa Idehpour, Adibvafa Fallahpour, Brandon Wang, Sukjun Hwang, BO WANG, Patrick Hsu, Hani Goodarzi, Albert Gu
摘要
Genomic foundation models have the potential to decode DNA syntax, yet face a fundamental tradeoff in their input representation. Standard fixed-vocabulary tokenizers fragment biologically meaningful motifs such as codons and regulatory elements, while nucleotide-level models preserve biological coherence but incur prohibitive computational costs for long contexts. We introduce dnaHNet, a state-of-the-art tokenizer-free autoregressive model that segments and models genomic sequences end-to-end. Using a differentiable dynamic chunking mechanism, dnaHNet compresses raw nucleotides into latent tokens adaptively, balancing compression with predictive accuracy. Pretrained on prokaryotic genomes, dnaHNet outperforms leading architectures including StripedHyena2 in scaling and efficiency. This recursive chunking yields quadratic FLOP reductions, enabling > 3× inference speedup over Transformers. On zero-shot tasks, dnaH-Net achieves superior performance in predicting protein variant fitness and gene essentiality, while automatically discovering hierarchical biological structures without supervision. These results establish dnaHNet as a scalable, interpretable framework for next-generation genomic modeling.
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- Efficiently Modeling Long Sequences with Structured State SpacesAlbert Gu, Karan Goel, Christopher RéICLR 2022 · 被引用 3,482 次
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- Byte Latent Transformer: Patches Scale Better Than TokensArtidoro Pagnoni, Ramakanth Pasunuru, Pedro Rodríguez, John Nguyen 等ACL 2025 · 被引用 116 次
- Dynamic Chunking for End-to-End Hierarchical Sequence ModelingSukjun Hwang, Brandon Wang, Albert GuICLR 2026 · 被引用 76 次
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