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UCE

Stanford SNAP
open weights / Overall score: 1.0

UCE is the Stanford SNAP lab's universal cell embedding model, a self-supervised transformer that maps single-cell transcriptomes from many tissues and species into one latent space. It ships 4-layer and 33-layer pretrained checkpoints and an evaluation script that embeds an AnnData dataset directly, with no labeling, training, or fine-tuning step.

The repository is an inference implementation; the pretraining corpus and the model's behavior are documented in the Nature paper rather than in the README. Verified 2026-09-10 via the GitHub API, the repository README and LICENSE, and the published paper.

Openness

3 high confidence
3.0
weights
open(ungated 4-layer and 33-layer checkpoints, fetched by the evaluation script or from Figshare)
data
documented-not-released(the paper describes the 36-million-cell Integrated Mega-scale Atlas corpus while the repository links processed paper datasets rather than the pretraining corpus)
code
partial(embedding and evaluation script only
license
CC-BY-4.0(governs the Figshare-hosted checkpoints

The checkpoints are freely downloadable and the corpus is described in the paper, but the repository ships only the code needed to embed a dataset, so the full-pipeline rungs are out of reach. The licence recorded here is the weights licence, not the repository's: the 33-layer checkpoint ships from Figshare item 24320806, whose record states CC BY 4.0, while the repository LICENSE is MIT and covers the code. Under multi_sku_rule the distributed weights govern, which resolves the tier to permissive_non_osi rather than osi. The score is unchanged - the walk reaches the fallthrough either way.

Adoption

1 medium confidence
1.0

No Hugging Face or package artifact is declared, so 338 GitHub stars are the last-resort signal; checkpoints are served from the authors' own hosting and from Figshare, neither of which reports a download count.

Capability

1 high confidence
1.0

The absent adaptation pathway is a positive claim by the publisher rather than a gap in the evidence. The model emits embeddings rather than generated outputs, takes one transcriptomic modality, and operates at one scale; embedding cells from many species is coverage, not a second instrument.

Verified 2026-09-10