BiologybioRxiv

Ranked by formulaVerdict: Notable

Few-shot regulatory sequence design with a genomic language model

A central challenge in generative biology is translating knowledge learned from natural sequences and experiments into designs with desired functions.

By Hie, Hao, Liu +7

Score█████░░░░░4.6

Caveats

  • Preprint; not yet peer reviewed.

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Abstract

A central challenge in generative biology is translating knowledge learned from natural sequences and experiments into designs with desired functions. In-context learning (ICL) is an emergent capability of large language models that allows them to adapt to new tasks from a few examples without additional training, enabling these models to become general-purpose learners. Here, we show that the genome language model, Evo 2, exhibits generative ICL in biological sequence design. Prompting with just tens of examples conditions Evo 2 to generate novel and diverse regulatory DNA sequences without any additional training. Mechanistic analysis suggests that genomic ICL may originate from induction, similar to phenomena observed in natural language. Reinforcement learning leveraging sequence-to-function models as experiment-derived rewards further strengthens ICL. We first validate this approach by generating enhancers that drive cell-type-specific gene expression in three human cell lines. Extending this approach in vivo, enhancers designed using human regulatory element data selectively label layer 5 extratelencephalic neurons in the mouse cortex with high specificity and stronger activity than existing enhancers. Our study provides evidence of emergent properties in genomic sequence models and introduces a promising approach for improving functional conditioning in generative biology.

B. Hie, Y. A. Hao, M. Liu, D. Nori, G. Brixi, T. Lau, C. A. Ramakrishnan, D. Chang, R. Park, W. E. Allen

The editor's rubric

Heuristic review

Leverage4 / 5
A general-purpose tool used across several fields (Adam, ResNet, LoRA, next-generation sequencing).
24% of this desk’s rubric
Magnitude2 / 5
Solid incremental gain on a meaningful problem.
16% of this desk’s rubric
Evidence3 / 5
Solid: multiple benchmarks or cohorts, ablations, fair baselines, released code or data.
20% of this desk’s rubric
Novelty3 / 5
A genuinely new approach to an open problem.
20% of this desk’s rubric
Trajectory3 / 5
A clear path to scale.
10% of this desk’s rubric
Stakes2 / 5
Benefits a professional community (practitioners, clinicians, engineers).
10% of this desk’s rubric

Editor’s rationale

Heuristic triage from title and abstract text only, not a reading of the paper. Cues found: method (we report); breadth (general-purpose, many tasks, zero/few-shot); novelty (alternative to status quo); verification (multiple benchmarks, experimental validation); scale (improves with scale).

How the score was computed

rank-2026-10-18

Score█████░░░░░4.6

Score = 10 × (75% × adjusted merit / 10 + 15% × attention + 10% × freshness)

Desks place stronger verdicts first, then use this score to order work within the same verdict.

Merit
6.0 / 10
Weighted rubric, evidence-gated.
Adjusted merit
4.9 / 10
Shrunk toward the desk prior by editor confidence (46%).
Attention
0%
Citations, upvotes, points, mentions.
Freshness
88%
Half-life decay since publication.

No attention signals recorded yet.

The record

  • Reviewed by heuristic-v10 on Oct 31, 2026, 05:48 UTC. Paper type: method.
  • Categories: bioengineering
  • TOP, No.6 in the Biology edition of October 31, 2026.