Evidence map›Paper›PMID 41632592›Full record

ArticleBriefings in bioinformatics2026

BayesRare: Bayesian mixture model for population-level rare cell type detection in multi-subject single-cell RNA sequencing data.

Yinqiao Yan, Hao Wu

Abstract read
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Article in Briefings in bioinformatics, 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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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Yinqiao YanSchool of Mathematics, Statistics and Mechanics, Beijing University of Technology, No. 100 Pingleyuan, Beijing 100124, China.ORCID 0000-0001-6496-4536
Hao WuShenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, No. 1068 Xueyuan Avenue, Shenzhen 518055, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rare cell types in single-cell RNA sequencing (scRNA-seq) data often encode essential biological signals, such as early disease markers or key immune regulators. With advancing technologies, large-scale scRNA-seq cohorts from multiple subjects now enable population-level analyses of the prevalence, heterogeneity, and disease associations of rare cell populations. However, existing methods for rare cell detection are typically limited to single datasets and cannot effectively leverage cross-subject information. To tackle this challenge, we present BayesRare, a hierarchical Bayesian framework for population-level rare cell discovery in multi-subject scRNA-seq data. The method augments a Bayesian mixture model with a rare cluster indicator, supporting joint cell-type clustering and rare-population identification. By explicitly characterizing the statistical properties of rare cell types, BayesRare integrates evidence across subjects, quantifies uncertainty via posterior probabilities, and enables inference of group-level differences (e.g. patients versus controls). Across synthetic and three real datasets, BayesRare achieves superior precision, reduces false positives, and uncovers biologically meaningful disease-specific rare subtypes. The R package of BayesRare is available at https://github.com/yinqiaoyan/BayesRare.

Indexed as

Sequence Analysis, RNASingle-Cell AnalysisSoftwareAlgorithmsBayes TheoremHumansSingle-Cell Gene Expression Analysisgroup-specific cell populationshierarchical Bayesian clusteringmulti-subject integrationrare cell discoverysingle-cell transcriptomics

Identifiers

PMID41632592
PMCPMC12867491

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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.