Evidence map›Paper›PMID 41165609›Full record

ReviewBioinformatics (Oxford, England)2025

The cell as a token: high-dimensional geometry in language models and cell embeddings.

William Gilpin

Abstract readReview
In one paragraph

Review in Bioinformatics (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author.

William GilpinDepartment of Physics, The University of Texas at Austin, Austin, TX 78712, United States.ORCID 0000-0001-8666-6951

Funding

Chan Zuckerberg Initiative DAF DAF2023-329596NSF CMMI 2440490NSF DMS 2436233Silicon Valley Community Foundation
6 · The paper itself

Abstract

motivationSingle-cell sequencing technology maps cells to a high-dimensional space encoding their internal activity. Recently-proposed virtual cell models extend this concept, enriching cells' representations based on patterns learned from pretraining on vast cell atlases.

resultsThis review explores how advances in understanding the structure of natural language embeddings informs ongoing efforts to analyze single-cell datasets. Both fields process unstructured data by partitioning datasets into tokens embedded within a high-dimensional vector space. We discuss how the context of tokens influences the geometry of embedding space, and how low-dimensional manifolds shape this space's robustness and interpretation. We highlight how new developments in foundation models for language, such as interpretability probes and in-context reasoning, can inform efforts to construct cell atlases and train virtual cell models. AVAILABILITY AND IMPLEMENTATION: Code is available at https://github.com/williamgilpin/celltoken.

Indexed as

Computational BiologyModels, BiologicalNatural Language ProcessingSingle-Cell AnalysisHumansSoftware

Identifiers

PMID41165609
PMCPMC12619638

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.