Evidence map›Paper›PMID 40597595›Full record

ArticleBMC bioinformatics2025

Replacing normalizations with interval assumptions enhances differential expression and differential abundance analyses.

Kyle C McGovern, Justin D Silverman

Abstract read
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Article in BMC bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Kyle C McGovernProgram in Bioinformatics and Genomics, Pennsylvania State University, University Park, PA, USA.
Justin D SilvermanProgram in Bioinformatics and Genomics, Pennsylvania State University, University Park, PA, USA. jds6696@psu.edu.

Funding

DMS/NIGMS 1: Addressing Measurement Limitations for Sequence Count DataR01GM148972 · NIGMS · PENNSYLVANIA STATE UNIVERSITY, THE · PI SILVERMAN, JUSTIN D · 2022 to 2024
$600k
NIGMS NIH HHS R01 GM148972NIGMS NIH HHS R01GM148972-01
6 · The paper itself

Abstract

backgroundMethods for differential expression and differential abundance analysis often rely on normalization to address sample-to-sample variation in sequencing depth. However, normalizations imply strict, unrealistic assumptions about the unmeasured scale of biological systems (e.g., microbial load or total cellular transcription). Even slight errors in these assumptions introduce bias, leading to elevated false positive and negative rates.

resultsWe introduce interval assumptions as a generalization of normalizations. Unlike normalizations, our interval methods allow researchers to account for potential errors in assumptions about the system scale. Interval assumptions are also customizable and allow researchers to express more biologically plausible assumptions about scale. Interval assumptions even generalize Quantitative Microbiome Profiling (QMP), allowing researchers to account for errors in flow cytometry-based measurements of total cellular concentration. We develop a novel hypothesis testing framework that allows us to integrate interval assumptions into existing tools. We develop a modified version of the popular ALDEx2 method using interval assumptions rather than normalizations. Through real and simulated data analyses, we find that interval assumptions can dramatically decrease false positive rates (i.e., from 45% to 5%) while retaining or increasing statistical power. We also study interval assumptions under misspecification and show they still improve on normalizations.

conclusionsInterval assumptions enhance the rigor and reproducibility of differential expression and differential abundance analyses. Our results add to a growing body of literature arguing that normalizations should be replaced with alternative methods that allow researchers to account for scale uncertainty. However, compared to recent alternatives like scale models and sensitivity analyses, interval assumptions are easier to use, are more robust to misspecification, and have stronger and more interpretable inferential guarantees.

Indexed as

Computational BiologyGene Expression ProfilingAlgorithmsHumansMicrobiota

Identifiers

PMID40597595
PMCPMC12218962

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LicenceCC BY-NC-ND
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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.