多元微积分
协变量
计算机科学
微生物群
特征(语言学)
多样性(控制论)
广义线性模型
航程(航空)
线性模型
联想(心理学)
计算生物学
数据挖掘
遗传关联
人工智能
组合性原则
精炼(冶金)
丰度(生态学)
机器学习
成分数据
任务(项目管理)
相对物种丰度
数学
缺少数据
特征选择
先验与后验
链接(几何体)
简单(哲学)
生物
生物信息学
基因组
作者
William A. Nickols,Thomas Kuntz,Jiaxian Shen,Sagun Maharjan,Himel Mallick,Eric A. Franzosa,Kelsey N. Thompson,Jacob T. Nearing,Curtis Huttenhower
出处
期刊:Nature Methods
[Nature Portfolio]
日期:2026-01-15
卷期号:23 (3): 554-564
被引量:13
标识
DOI:10.1038/s41592-025-02923-9
摘要
Microbial community analysis typically involves determining which microbial features are associated with properties such as environmental or health phenotypes. This task is impeded by data characteristics, including sparsity (technical or biological) and compositionality. Here we introduce MaAsLin 3 (microbiome multivariable associations with linear models) to simultaneously identify both abundance and prevalence relationships in microbiome studies with modern, potentially complex designs. MaAsLin 3 can newly account for compositionality either experimentally (for example, quantitative PCR or spike-ins) or computationally, and it expands the range of testable biological hypotheses and covariate types. On a variety of synthetic and real datasets, MaAsLin 3 outperformed state-of-the-art differential abundance methods, and when applied to the Inflammatory Bowel Disease Multi-omics Database, MaAsLin 3 corroborated previously reported associations, identifying 77% with feature prevalence rather than abundance. In summary, MaAsLin 3 enables researchers to identify microbiome associations more accurately and specifically, especially in complex datasets.
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