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Ranked by formulaVerdict: Notable

MUSS: A Multi-scale and Sequence-based Model for Single-cell Gene Regulation

Modeling gene regulation in single cells requires jointly representing DNA sequence, chromatin accessibility, and gene expression across regulatory scales.

By Zheng, Vahidi, Jin +7

Score████░░░░░░3.8

VerdictWorth a reader's time today.

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Abstract

Modeling gene regulation in single cells requires jointly representing DNA sequence, chromatin accessibility, and gene expression across regulatory scales. Sequence-based models capture DNA-level regulatory grammar but often lack cell-level resolution, whereas many single-cell omics models represent genes and peaks as fixed-vocabulary tokens without their underlying sequence. Here, we present MUSS, a sequence-based multi-scale model for single-cell gene regulation that preserves both DNA-level and cell-level resolution. MUSS derives peak- and gene-level representations from DNA using a frozen pre-trained sequence encoder and integrates them through peak-peak self-attention and distance-biased peak-gene interactions. Peak masked language modeling followed by training on paired scATAC-seq and scRNA-seq aligns these representations with cell-specific regulatory states. Across gene expression prediction, enhancer-gene linking, motif-guided regulatory prioritization, and zero-shot cell clustering, MUSS achieves strong performance against sequence-based and single-cell omics baselines. It further predicts expression for genes and peaks unseen during task training. These results support sequence-grounded, multi-scale representations for decoding cell-type-specific regulatory programs. Code, datasets, and model checkpoints are available at https://github.com/Lotfollahi-lab/MUSS_neurips26.

Kangjie Zheng, Amirhossein Vahidi, Liying Jin, Joseph Clarke, Vijaya Baskar MS, Connor Rogerson, Mengji Zhang, Muzlifah Haniffa, Anshul Kundaje, Mo Lotfollahi

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.
18% of this desk’s rubric
Evidence3 / 5
Solid: multiple benchmarks or cohorts, ablations, fair baselines, released code or data.
14% of this desk’s rubric
Novelty3 / 5
A genuinely new approach to an open problem.
16% of this desk’s rubric
Trajectory3 / 5
A clear path to scale.
18% 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 propose); breadth (zero/few-shot); verification (held-out test, code released); scale (scalable).

How the score was computed

rank-2026-10-18

Score████░░░░░░3.8

Score = 10 × (65% × adjusted merit / 10 + 25% × attention + 10% × freshness)

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

Merit
5.9 / 10
Weighted rubric, evidence-gated.
Adjusted merit
4.7 / 10
Shrunk toward the desk prior by editor confidence (38%).
Attention
0%
Citations, upvotes, points, mentions.
Freshness
77%
Half-life decay since publication.

No attention signals recorded yet.

The record

  • Reviewed by heuristic-v10 on Nov 6, 2026, 13:39 UTC. Paper type: method.
  • Categories: cs.AI, q-bio.GN
  • TOP, No.4 in the Biology edition of November 6, 2026.