Evidence map›Paper›PMID 39807898›Full record

ArticleMicrobiology spectrum2025

A sensitivity analysis of methodological variables associated with microbiome measurements.

Samuel P Forry, Stephanie L Servetas, Jennifer N Dootz, Monique E Hunter, Jason G Kralj, James J Filliben, Scott A Jackson

Abstract read
In one paragraph

Article in Microbiology spectrum, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–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

5 citing papers in PubMed.

  1. Article
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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

7 authors.

Samuel P ForryComplex Microbial Systems Group, National Institute of Standards and Technology (NIST), Gaithersburg, Maryland, USA.ORCID 0009-0000-8200-0327
Stephanie L ServetasComplex Microbial Systems Group, National Institute of Standards and Technology (NIST), Gaithersburg, Maryland, USA.
Jennifer N DootzComplex Microbial Systems Group, National Institute of Standards and Technology (NIST), Gaithersburg, Maryland, USA.
Monique E HunterComplex Microbial Systems Group, National Institute of Standards and Technology (NIST), Gaithersburg, Maryland, USA.
Jason G KraljComplex Microbial Systems Group, National Institute of Standards and Technology (NIST), Gaithersburg, Maryland, USA.ORCID 0000-0003-4565-1176
James J FillibenMultimodal Information Group, National Institute of Standards and Technology (NIST), Gaithersburg, Maryland, USA.
Scott A JacksonComplex Microbial Systems Group, National Institute of Standards and Technology (NIST), Gaithersburg, Maryland, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The experimental methods employed during metagenomic sequencing analyses of microbiome samples significantly impact the resulting data and typically vary substantially between laboratories. In this study, a full factorial experimental design was used to compare the effects of a select set of methodological choices (sample, operator, lot, extraction kit, variable region, and reference database) on the analysis of biologically diverse stool samples. For each parameter investigated, a main effect was calculated that allowed direct comparison both between methodological choices (bias effects) and between samples (real biological differences). Overall, methodological bias was found to be similar in magnitude to real biological differences while also exhibiting significant variations between individual taxa, even between closely related genera. The quantified method biases were then used to computationally improve the comparability of data sets collected under substantially different protocols. This investigation demonstrates a framework for quantitatively assessing methodological choices that could be routinely performed by individual laboratories to better understand their metagenomic sequencing workflows and to improve the scope of the datasets they produce.IMPORTANCEMethod-specific bias is a well-recognized challenge in metagenomic sequencing characterization of microbiome samples, but rigorous bias quantification is challenging. This report details a full factorial exploration of 48 experimental protocols by systematically varying microbiome sample, iterations of material production, laboratory personnel, DNA extraction kit, marker gene selection, and reference databases. Quantification of the biases associated with each parameter revealed similar magnitudes of variation arising from real biological differences and from varied analysis procedures. Furthermore, these measurement biases varied substantially with taxa, even between closely related genera. However, computational correction of method bias using a reference material was demonstrated that significantly harmonized metagenomic sequencing results collected using different analysis protocols.

Indexed as

BacteriaMetagenomicsMicrobiotaFecesGastrointestinal MicrobiomeHumansbiasmeasurementmetagenomic sequencingmicrobiome

Identifiers

PMID39807898
PMCPMC11792480

What OpenQuestion holds

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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.