Evidence map›Paper›PMID 37983251›Full record

ArticlePLoS computational biology2023

Addressing erroneous scale assumptions in microbe and gene set enrichment analysis.

Kyle C McGovern, Michelle Pistner Nixon, Justin D Silverman

Abstract read
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Kyle C McGovernProgram in Bioinformatics and Genomics, Pennsylvania State University, State College, Pennsylvania, United States of America.
Michelle Pistner NixonCollege of Information Sciences and Technology, Pennsylvania State University, State College, Pennsylvania, United States of America.
Justin D SilvermanProgram in Bioinformatics and Genomics, Pennsylvania State University, State College, Pennsylvania, United States of America.ORCID https://orcid.org/0000-0002-3063-2098

Funding

Medical Scientist Training Program Training GrantT32GM145449 · NIGMS · DUKE UNIVERSITY · PI Christopher D Kontos · 2022 to 2026
$6.6M
Computation, Bioinformatics, and Statistics (CBIOS) Training ProgramT32GM102057 · NIGMS · PENNSYLVANIA STATE UNIVERSITY, THE · PI CHIAROMONTE, FRANCESCA, GIRIRAJAN, SANTHOSH · 2013 to 2022
$2.7M
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 T32 GM102057NIGMS NIH HHS T32 GM145449
6 · The paper itself

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.

Identifiers

PMID37983251
PMCPMC10695402

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.