ArticlePLoS computational biology2023
Addressing erroneous scale assumptions in microbe and gene set enrichment analysis.
Article in PLoS computational biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.
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Who cites it
10 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Vaginal metatranscriptome meta-analysis reveals functional BV subgroups and novel colonisation strategies.Microbiome · 2024Pooled it
- Not every gene is special: Modelling scale controls the false discovery rate when analysing high-throughput sequencing data.PLoS computational biology · 2026Article
- Scale reliant mixed effects models enhance microbiome data analysis.Microbiome · 2026Article
- Incorporating Scale Uncertainty into Differential Expression Analyses Using ALDEx2.Current protocols · 2026Article
- Uncertainty Modeling Outperforms Machine Learning for Microbiome Data Analysis.bioRxiv : the preprint server for biology · 2025Article
- Explicit Scale Simulation for analysis of RNA-sequencing count data with ALDEx2.NAR genomics and bioinformatics · 2025Article
- Replacing normalizations with interval assumptions enhances differential expression and differential abundance analyses.BMC bioinformatics · 2025Article
- Incorporating scale uncertainty in microbiome and gene expression analysis as an extension of normalization.Genome biology · 2025Article
- Beyond Normalization: Incorporating Scale Uncertainty in Microbiome and Gene Expression Analysis.bioRxiv : the preprint server for biology · 2024Article
- Use of intrauterine dextrose as an alternative to systemic antibiotics for treatment of clinical metritis in dairy cattle: a microbiome perspective.Frontiers in veterinary science · 2024Article
Corrections and comments
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Authors and funding
3 authors.
Funding
Abstract
By applying Differential Set Analysis (DSA) to sequence count data, researchers can determine whether groups of microbes or genes are differentially enriched. Yet sequence count data suffer from a scale limitation: these data lack information about the scale (i.e., size) of the biological system under study, leading some authors to call these data compositional (i.e., proportional). In this article, we show that commonly used DSA methods that rely on normalization make strong, implicit assumptions about the unmeasured system scale. We show that even small errors in these scale assumptions can lead to positive predictive values as low as 9%. To address this problem, we take three novel approaches. First, we introduce a sensitivity analysis framework to identify when modeling results are robust to such errors and when they are suspect. Unlike standard benchmarking studies, this framework does not require ground-truth knowledge and can therefore be applied to both simulated and real data. Second, we introduce a statistical test that provably controls Type-I error at a nominal rate despite errors in scale assumptions. Finally, we discuss how the impact of scale limitations depends on a researcher's scientific goals and provide tools that researchers can use to evaluate whether their goals are at risk from erroneous scale assumptions. Overall, the goal of this article is to catalyze future research into the impact of scale limitations in analyses of sequence count data; to illustrate that scale limitations can lead to inferential errors in practice; yet to also show that rigorous and reproducible scale reliant inference is possible if done carefully.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.