混合模型
贝叶斯概率
计算机科学
编码
计算生物学
杠杆(统计)
聚类分析
推论
层次聚类
贝叶斯推理
人工智能
马尔科夫蒙特卡洛
后验概率
贝叶斯分层建模
统计模型
模式识别(心理学)
先验概率
数据挖掘
核糖核酸
电池类型
贝叶斯定理
数据类型
细胞
R包
星团(航天器)
DNA测序
罕见事件
合成数据
钥匙(锁)
分层数据库模型
生物
作者
Yinqiao Yan,Zhigang Wu
摘要
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.
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