Sparse Bayesian Group Factor Model for Feature Interactions in Multiple Count Tables Data
多计数表特征交互的稀疏贝叶斯组因子模型AI 解读 ↓
本页整理公开书目信息,不生成学术质量评分。AI 解读根据题名及所注明的摘要或原文片段生成,未完成全文核验,可能有误;具体假设、证明与结论请核对原文。摘要保留来源文本,未经模型改写。
DOI 首次登记不等于接收或发表日期。部分更正、评论等条目没有独立摘要;缺少可靠材料时保留待补状态。
引用量采用 OpenAlex 单条关联记录,不合计多个记录;关联记录可能包含正式发表版本,不等于此版本单独引用。缺失不视为零,引用指标不代表论文质量。
关注作者按书目中的完整姓名匹配,同名和姓名变体需人工辨别。相关论文先按共享细分方向和具体方法排列,再参考通用方法与发表日期。
AI 根据所提供的论文材料归类:摘要研究微生物计数数据的通用贝叶斯因子模型,没有直接支持宏观因子或微观网络计量分类的文本依据。
多计数表特征交互的稀疏贝叶斯组因子模型AI 解读 ↓
正在核对关联版本…
正在核对对应版本的资源…
Group factor models have been developed to infer relationships between multiple co-occurring multivariate continuous responses. Motivated by complex count data from multi-domain microbiome studies using next-generation sequencing, we develop a sparse Bayesian group factor model (Sp-BGFM) for multiple count table data that captures the interaction between microorganisms in different domains. Sp-BGFM uses a rounded kernel mixture model using a Dirichlet process (DP) prior with log-normal mixture kernels for count vectors. A group factor model is used to model the covariance matrix of the mixing kernel that describes microorganism interaction. We construct a Dirichlet-Horseshoe (Dir-HS) shrinkage prior and use it as a joint prior for factor loading vectors. Joint sparsity induced by a Dir-HS prior greatly improves the performance in high-dimensional applications. We further model the effects of covariates on microbial abundances using regression. The semiparametric model flexibly accommodates large variability in observed counts and excess zero counts and provides a basis for robust estimation of the interaction and covariate effects. We evaluate Sp-BGFM using simulation studies and real data analysis, comparing it to popular alternatives. Our results highlight the necessity of joint sparsity induced by the Dir-HS prior, and the benefits of a flexible DP model for baseline abundances.