Evidence map›Paper›PMID 41516004›Full record

ArticleInternational journal of molecular sciences2025

scANMF: Prior Knowledge and Graph-Regularized NMF for Accurate Cell Type Annotation in scRNA-seq.

Weilai Chi, Ying Zheng, Huaying Fang, Shi Shi

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Article in International journal of molecular sciences, 2025. 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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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Weilai ChiSchool of Mathematical Sciences, Capital Normal University, Beijing 100048, China.ORCID 0000-0002-0637-747X
Ying ZhengSchool of Mathematical Sciences, Capital Normal University, Beijing 100048, China.ORCID 0009-0008-0326-9263
Huaying FangBeijing Advanced Innovation Center for Imaging Theory and Technology, Capital Normal University, Beijing 100089, China.ORCID 0000-0002-7693-8260
Shi ShiSchool of Economics, Hangzhou Dianzi University, Hangzhou 310018, China.ORCID 0009-0006-3662-6517

Funding

Zhejiang Provincial Basic Public Welfare Research Program's Natural Science Foundation Exploration Project LQ23A010017
6 · The paper itself

Abstract

Single-cell RNA sequencing (scRNA-seq) provides a high-resolution view of cellular heterogeneity, yet accurate cell-type annotation remains challenging due to data sparsity, technical noise, and variability across tissues, platforms, and species. Many existing annotation tools depend on a single form of prior knowledge, such as marker genes or reference profiles, which can limit performance when these resources are incomplete or inconsistent. Here, we present scANMF, a prior- and graph-regularized non-negative matrix factorization framework that integrates marker-gene information, partial label supervision, and the local manifold structure into a unified annotation model. scANMF factorizes the expression matrix into interpretable gene-factor and cell-factor representations, enabling accurate annotation in settings with limited or noisy prior information. Across multiple real scRNA-seq collections, scANMF achieved a high annotation accuracy in within-dataset, cross-platform, and cross-species evaluations. The method remained stable under varying levels of label sparsity and marker-gene noise and showed a broad robustness to hyperparameter choices. Ablation analyses indicated that marker priors, label supervision, and graph regularization contribute complementary information to the overall performance. These results support scANMF as a practical and robust framework for single-cell annotation, particularly in applications where high-quality prior knowledge is restricted.

Indexed as

Computational BiologyMolecular Sequence AnnotationRNA-SeqSequence Analysis, RNASingle-Cell AnalysisSoftwareAlgorithmsAnimalsHumansSingle-Cell Gene Expression Analysiscell-type annotationgraph regularizationnon-negative matrix factorizationprior knowledge integrationrobustness to noisesemi-supervised learningsingle-cell RNA sequencing

Identifiers

PMID41516004
PMCPMC12785987

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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.