Genomic variations and chromosomal abnormalities Open access Peer reviewed

Advancing regulatory variant effect prediction with AlphaGenome

Natasha S. Latysheva, Jun Cheng, Guido Novati, Kyle R. Taylor and 22 more

Nature | Jan 28, 2026 | 127 citations

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AlphaGenome, a unified DNA sequence model, takes as input 1-Mb of DNA sequence and predicts thousands of functional genomic tracks up to single-base-pair resolution across diverse modalities, outperforms existing models in variant effect prediction and enables comprehensive genomic analysis.

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Abstract Deep learning models that predict functional genomic measurements from DNA sequences are powerful tools for deciphering the genetic regulatory code. Existing methods involve a trade-off between input sequence length and prediction resolution, thereby limiting their modality scope and performance 1–5 . We present AlphaGenome, a unified DNA sequence model, which takes as input 1 Mb of DNA sequence and predicts thousands of functional genomic tracks up to single-base-pair resolution across diverse modalities. The modalities include gene expression, transcription initiation, chromatin accessibility, histone modifications, transcription factor binding, chromatin contact maps, splice site usage and splice junction coordinates and strength. Trained on human and mouse genomes, AlphaGenome matches or exceeds the strongest available external models in 25 of 26 evaluations of variant effect prediction. The ability of AlphaGenome to simultaneously score variant effects across all modalities accurately recapitulates the mechanisms of clinically relevant variants near the TAL1 oncogene 6 . To facilitate broader use, we provide tools for making genome track and variant effect predictions from sequence.

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Natasha S. Latysheva

middle | Google DeepMind (United Kingdom) | ORCID 0000-0003-3119-0567

Jun Cheng

middle | Google DeepMind (United Kingdom) | ORCID 0000-0001-5573-9791

Guido Novati

middle | Google DeepMind (United Kingdom) | ORCID 0000-0003-0681-4892

Kyle R. Taylor

middle | Google DeepMind (United Kingdom) | ORCID 0000-0002-4586-8300

Tom Ward

middle | Google DeepMind (United Kingdom)

Clare Bycroft

middle | Google DeepMind (United Kingdom) | ORCID 0000-0002-1139-0732

Lauren Nicolaisen

middle | Google DeepMind (United Kingdom)

Eirini Arvaniti

middle | Google DeepMind (United Kingdom) | ORCID 0000-0003-3045-9309

Joshua Pan

middle | Google DeepMind (United Kingdom)

Raina W. Thomas

middle | Google DeepMind (United Kingdom) | ORCID 0000-0001-8027-3460

Vincent Dutordoir

middle | Google DeepMind (United Kingdom)

Matteo Perino

middle | Google DeepMind (United Kingdom) | ORCID 0000-0001-7173-0252

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BibTeX

@article{Latysheva2026Advancing,
  title = {Advancing regulatory variant effect prediction with AlphaGenome},
  author = {Natasha S. Latysheva and Jun Cheng and Guido Novati and Kyle R. Taylor and Tom Ward and Clare Bycroft and Lauren Nicolaisen and Eirini Arvaniti and Joshua Pan and Raina W. Thomas and Vincent Dutordoir and Matteo Perino and S. P. M. Boer De and Alexander Karollus and Adam Gayoso and Toby Sargeant and Anne Mottram and Lai Hong Wong and Pavol Drotár and Adam R. Kosiorek and Andrew Senior and Richard Tanburn and Taylor Applebaum and Souradeep Basu and Demis Hassabis and Pushmeet Kohli},
  journal = {Nature},
  year = {2026},
  doi = {10.1038/s41586-025-10014-0},
  url = {https://doi.org/10.1038/s41586-025-10014-0}
}

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