ZINQ-L: a zero-inflated quantile approach for differential abundance analysis of longitudinal microbiome data.

IF 2.8 3区 生物学 Q2 GENETICS & HEREDITY Frontiers in Genetics Pub Date : 2025-01-29 eCollection Date: 2024-01-01 DOI:10.3389/fgene.2024.1494401
Shuai Li, Runzhe Li, John R Lee, Ni Zhao, Wodan Ling
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Abstract

Background: Identifying bacterial taxa associated with disease phenotypes or clinical treatments over time is critical for understanding the underlying biological mechanism. Association testing for microbiome data is already challenging due to its complex distribution that involves sparsity, over-dispersion, heavy tails, etc. The longitudinal nature of the data adds another layer of complexity - one needs to account for the within-subject correlations to avoid biased results. Existing longitudinal differential abundance approaches usually depend on strong parametric assumptions, such as zero-inflated normal or negative binomial. However, the complex microbiome data frequently violate these distributional assumptions, leading to inflated false discovery rates. In addition, the existing methods are mostly mean-based, unable to identify heterogeneous associations such as tail events or subgroup effects, which could be important biomedical signals.

Methods: We propose a zero-inflated quantile approach for longitudinal (ZINQ-L) microbiome differential abundance test. A mixed-effects quantile rank-score-based test was proposed for hypothesis testing, which consists of a test in mixed-effects logistic model for the presence-absence status of the investigated taxon, and a series of mixed-effects quantile rank-score tests adjusted for zero inflation given its presence. As a regression method with minimal distributional assumptions, it is robust to the complex microbiome data, controlling false discovery rate, and is flexible to adjust for important covariates. Its comprehensive examination of the abundance distribution enables the identification of heterogeneous associations, improving the testing power.

Results: Extensive simulation studies and an application to a real kidney transplant microbiome study demonstrate the improved power of ZINQ-L in detecting true signals while controlling false discovery rates.

Conclusion: ZINQ-L is a zero-inflated quantile-based approach for detecting individual taxa associated with outcomes or exposures in longitudinal microbiome studies, providing a robust and powerful option to improve and complement the existing methods in the field.

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纵向微生物组数据差异丰度分析的零膨胀分位数方法。
背景:随着时间的推移,识别与疾病表型或临床治疗相关的细菌分类群对于理解潜在的生物学机制至关重要。微生物组数据的关联测试已经具有挑战性,因为它的分布复杂,涉及稀疏性、过度分散、重尾等。数据的纵向特性增加了另一层复杂性——人们需要考虑主题内部的相关性,以避免有偏差的结果。现有的纵向差异丰度方法通常依赖于强参数假设,如零膨胀正态或负二项。然而,复杂的微生物组数据经常违反这些分布假设,导致虚高的错误发现率。此外,现有的方法大多是基于均值的,无法识别异质性关联,如尾部事件或亚组效应,这可能是重要的生物医学信号。方法:采用零膨胀分位数法进行纵向(ZINQ-L)微生物组差异丰度检测。提出了一种基于混合效应分位数秩-分数的假设检验方法,该方法包括对调查分类单元存在-不存在状态的混合效应逻辑模型检验,以及在存在情况下对零膨胀进行调整的一系列混合效应分位数秩-分数检验。作为一种具有最小分布假设的回归方法,它对复杂的微生物组数据具有较强的鲁棒性,控制了错误发现率,并且可以灵活地调整重要的协变量。它对丰度分布的全面检查能够识别异质关联,提高测试能力。结果:广泛的模拟研究和在真实肾脏移植微生物组研究中的应用表明,ZINQ-L在检测真实信号的同时控制错误发现率方面的能力有所提高。结论:ZINQ-L是一种基于零膨胀分位数的方法,用于检测与纵向微生物组研究结果或暴露相关的单个分类群,为改进和补充现有方法提供了一个强大的选择。
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来源期刊
Frontiers in Genetics
Frontiers in Genetics Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
5.50
自引率
8.10%
发文量
3491
审稿时长
14 weeks
期刊介绍: Frontiers in Genetics publishes rigorously peer-reviewed research on genes and genomes relating to all the domains of life, from humans to plants to livestock and other model organisms. Led by an outstanding Editorial Board of the world’s leading experts, this multidisciplinary, open-access journal is at the forefront of communicating cutting-edge research to researchers, academics, clinicians, policy makers and the public. The study of inheritance and the impact of the genome on various biological processes is well documented. However, the majority of discoveries are still to come. A new era is seeing major developments in the function and variability of the genome, the use of genetic and genomic tools and the analysis of the genetic basis of various biological phenomena.
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