Evidence map›Paper›PMID 42060707›Full record

ArticlePLoS computational biology2026

Cell type annotation for scATAC-seq via DNA large language model and graph domain adaptation.

Yan Liu, Sheng Guan, He Yan, Long-Chen Shen, Ji-Peng Qiang, Guo Wei

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Article in PLoS computational biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Yan LiuSchool of Information and Artificial Intelligence, Yangzhou University, Yangzhou, Jiangsu, China.
Sheng GuanSchool of Information and Artificial Intelligence, Yangzhou University, Yangzhou, Jiangsu, China.
He YanCollege of Information Science and Technology & Artificial Intelligence, Nanjing Forestry University, Nanjing, Jiangsu, China.
Long-Chen ShenSchool of Computer Science and Engineering, Nanjing University of Science and Technology, Nanjing, Jiangsu, China.
Ji-Peng QiangSchool of Information and Artificial Intelligence, Yangzhou University, Yangzhou, Jiangsu, China.
Guo WeiSchool of Computer Science and Information Engineering, Bengbu University, Bengbu, Anhui, China.ORCID https://orcid.org/0000-0002-2525-1776

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single-cell ATAC-seq (scATAC-seq) enables the exploration of chromatin accessibility at single-cell resolution, offering critical insights into gene regulation. Accurate cell type annotation is a fundamental prerequisite in scATAC-seq analysis. While cross-modality annotation methods leverage scRNA-seq data for label transfer, they often suffer from modality mismatch and signal distortion. Intra-modality annotation, which utilizes only scATAC-seq reference data, has gained attention for its biological consistency. However, existing methods are limited by insufficient sequence representation and lack of neighborhood modeling during domain adaptation. To address these limitations, we propose scLLMDA, a novel framework for scATAC-seq cell type annotation via DNA large language model and graph-based domain adaptation (GDA). scLLMDA uses a pretrained DNA-specific language model to generate contextual embeddings of peak sequences, which are then integrated with accessibility information to represent individual cells. We construct similarity-based cell graphs for both source and target datasets, and apply a graph neural network to align domains while preserving local structural context. Our approach captures rich sequence semantics and neighborhood dependencies, enabling more accurate and robust cell type annotation across datasets. Extensive experiments on multiple benchmarks demonstrate that scLLMDA outperforms existing methods in accuracy. The source code and implementation of scLLMDA are publicly available at: https://github.com/sheng-guan-2001/scLLMDA.

Indexed as

Chromatin Immunoprecipitation SequencingMolecular Sequence AnnotationSingle-Cell AnalysisAlgorithmsAnimalsComputational BiologyDNAGraph Neural NetworksHumansLarge Language ModelsDNA

Identifiers

PMID42060707
PMCPMC13132462

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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.