Evidence map›Paper›PMID 42635202›Full record

ArticleBioinformatics (Oxford, England)2026

CellTypeAI: cell annotation for scRNA-seq using local generative-AI.

Rufus H Daw, Harry R Deijnen, Magnus Rattray, John R Grainger

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2026. 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

4 authors.

Rufus H DawLydia Becker Institute of Immunology and Inflammation, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, M13 9PL, United Kingdom.ORCID 0000-0003-1258-937X
Harry R DeijnenLydia Becker Institute of Immunology and Inflammation, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, M13 9PL, United Kingdom.
Magnus RattrayLydia Becker Institute of Immunology and Inflammation, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, M13 9PL, United Kingdom.ORCID 0000-0001-8196-5565
John R GraingerLydia Becker Institute of Immunology and Inflammation, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, M13 9PL, United Kingdom.ORCID 0000-0002-4052-5923

Funding

Centre of Research Excellence in Exposome Immunology UKRI/MR/B000935/1Leducq Foundation Transatlantic Network of Excellence 19CVD01Medical Research CouncilMRC Doctoral Training ProgrammeSenior Fellowship awarded by The Kennedy Trust for Rheumatology ResearchUKRI-EPSRC EP/Y028805/1Wellcome TrustWellcome Trust 227415/Z/23/Z
6 · The paper itself

Abstract

motivationSingle-cell RNA sequencing (scRNA-seq) cell annotation techniques rely on the matching of known defining marker genes to a given cell population. However, these methods may lack robustness to dynamic fluctuations in cell marker expression between patients, samples and pathologies. The advent of easy-to-implement predictive technologies, like generative-AI (gen-AI), has facilitated the introduction of computational workflows that improve otherwise inaccurate context-dependent cell type annotation. Here, we introduce CellTypeAI, a streamlined, scalable program developed for tissue context-dependent cell annotation of scRNA-seq datasets using modern gen-AI models, enhanced by retrieval augmented generation methods.

resultsOur implementation builds upon local gen-AI hosting technologies and directly integrates into scRNA-seq analysis pipelines. We show that CellTypeAI provides improved annotation accuracy compared to current conventional annotation methods and nascent cloud-based gen-AI approaches. As CellTypeAI leverages locally-run AI models, it can be applied to sensitive datasets, unlike approaches utilising online gen-AI tools such as ChatGPT, DeepSeek, or Claude. CellTypeAI presents a novel solution for tissue-specific cell type identification, overcoming traditional marker-based limitations via locally-deployed gen-AI models. AVAILABILITY AND IMPLEMENTATION: The source code is available at: https://github.com/rhdaw/CellTypeAI.

Indexed as

Computational BiologyMolecular Sequence AnnotationRNA-SeqSequence Analysis, RNASingle-Cell AnalysisSoftwareGenerative Artificial IntelligenceHumansSingle-Cell Gene Expression Analysis

Identifiers

PMID42635202
PMCPMC13501282

What OpenQuestion holds

Textmetadata
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.