Rarefaction is better than robust Aitchison PCA and other compositional data analysis methods at controlling for uneven sequencing effort.

IF 5.2 2区 生物学 Q1 MICROBIOLOGY
mSystems Pub Date : 2026-10-20 Epub Date: 2026-09-30 DOI:10.1128/msystems.00930-26
Patrick D Schloss
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引用次数: 0

Abstract

Amplicon sequencing typically results in a wide distribution in the number of sequences obtained from each sample. How best to account for this variation has been a persistent problem in the microbial ecology literature. Historically, rarefaction has been used in ecology and this practice was adopted by microbial ecologists. However, rarefaction has been strongly criticized, leading to the development of compositional data analysis and normalization methods. Therefore, I reassessed the benchmarking data that were generated by the developers of one such method, robust Aitchison PCA. I found numerous problems in the Python code that led to the support of robust Aitchison PCA. These problems extended to the creation of simulated data sets, implementation of machine learning methods, and choice of analysis parameters. Furthermore, the analysis of the simulated and case study data sets was done in a manner that was foreign to standard microbiome analyses. I corrected the problems in the original code, added data sets with smaller effect sizes, and expanded the collection of methods that purport to correct for uneven sequencing effort. Contrary to the claims of the original analysis, robust Aitchison PCA was not insensitive to uneven sequencing effort and did not perform as well as rarefaction. In fact, even using the benchmarking framework from the original analysis, rarefaction outperformed robust Aitchison PCA, other compositional data analysis methods, and other normalization methods. Rarefaction remains the preferred method of controlling for uneven sampling effort in amplicon sequence studies.

Importance: Efforts to connect the structure of microbial communities with environmental processes and host health have captured widespread interest among scientists and the general public. The methods used to generate the sequencing data that are fundamental to these efforts result in wide variation in the number of sequences per sample. This variation and how to account for it can have detrimental effects on the ability to draw valid conclusions. Compositional data analysis methods, including robust Aitchison principal component analysis (PCA), have grown in popularity for mitigating these effects and have been proposed as alternatives to rarefaction. In this study, I reviewed and fixed the code that was used to benchmark robust Aitchison PCA and expanded the analysis. With this improved and expanded analysis, I found that rarefaction was still superior to robust Aitchison PCA and other methods of controlling for uneven sequencing effort.

在控制不均匀排序努力方面,Rarefaction优于稳健的Aitchison PCA和其他成分数据分析方法。
扩增子测序通常导致从每个样品获得的序列数量分布广泛。如何最好地解释这种变化一直是微生物生态学文献中一个持续存在的问题。从历史上看,稀薄已经在生态学中使用,这种做法被微生物生态学家采用。然而,稀疏性一直受到强烈的批评,导致了成分数据分析和归一化方法的发展。因此,我重新评估了由这样一种方法的开发人员生成的基准数据,稳健的艾奇逊PCA。我在Python代码中发现了许多问题,这些问题导致了对健壮的Aitchison PCA的支持。这些问题扩展到模拟数据集的创建、机器学习方法的实现以及分析参数的选择。此外,模拟和案例研究数据集的分析以一种与标准微生物组分析不同的方式完成。我纠正了原始代码中的问题,添加了具有较小效应大小的数据集,并扩展了旨在纠正不均匀排序工作的方法集合。与原始分析的主张相反,稳健的艾奇逊PCA对不均匀的测序工作并不敏感,并且没有表现得像稀疏一样好。事实上,即使使用原始分析中的基准测试框架,稀疏也优于稳健的Aitchison PCA、其他成分数据分析方法和其他归一化方法。在扩增子序列研究中,稀疏仍然是控制不均匀采样努力的首选方法。重要性:将微生物群落结构与环境过程和宿主健康联系起来的努力引起了科学家和公众的广泛兴趣。用于生成测序数据的方法是这些努力的基础,导致每个样本的序列数量变化很大。这种差异以及如何解释这种差异会对得出有效结论的能力产生不利影响。组成数据分析方法,包括稳健的艾奇逊主成分分析(PCA),已经越来越受欢迎,以减轻这些影响,并被提议作为稀疏的替代方案。在本研究中,我审查并修复了用于对稳健的Aitchison PCA进行基准测试的代码,并扩展了分析。通过这种改进和扩展的分析,我发现rarefaction仍然优于稳健的Aitchison PCA和其他控制不均匀测序努力的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
mSystems
mSystems Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
10.50
自引率
3.10%
发文量
308
审稿时长
13 weeks
期刊介绍: mSystems™ will publish preeminent work that stems from applying technologies for high-throughput analyses to achieve insights into the metabolic and regulatory systems at the scale of both the single cell and microbial communities. The scope of mSystems™ encompasses all important biological and biochemical findings drawn from analyses of large data sets, as well as new computational approaches for deriving these insights. mSystems™ will welcome submissions from researchers who focus on the microbiome, genomics, metagenomics, transcriptomics, metabolomics, proteomics, glycomics, bioinformatics, and computational microbiology. mSystems™ will provide streamlined decisions, while carrying on ASM''s tradition of rigorous peer review.
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