Evidence map›Paper›PMID 42493665›Full record

ArticleMetabolomics : Official journal of the Metabolomic Society2026

Integrated workflow for univariate and multivariate evaluation of batch correction reliability.

Elfried Salanon, Blandine Comte, Delphine Centeno, Stéphanie Durand, Estelle Pujos-Guillot, Julien Boccard

Abstract read
In one paragraph

Article in Metabolomics : Official journal of the Metabolomic Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors.

Elfried SalanonUniversité Clermont Auvergne, INRAE, UNH, Plateforme d'Exploration du Métabolisme, MetaboHUB Clermont, F63122 Saint-Genès Champanelle, Clermont-Ferrand, France. elfried.salanon@gmail.com.ORCID http://orcid.org/0009-0007-7560-2144
Blandine ComteUniversité Clermont Auvergne, INRAE, UNH, Plateforme d'Exploration du Métabolisme, MetaboHUB Clermont, F63122 Saint-Genès Champanelle, Clermont-Ferrand, France.ORCID http://orcid.org/0000-0002-4662-6581
Delphine CentenoUniversité Clermont Auvergne, INRAE, UNH, Plateforme d'Exploration du Métabolisme, MetaboHUB Clermont, F63122 Saint-Genès Champanelle, Clermont-Ferrand, France.ORCID http://orcid.org/0000-0002-2747-6290
Stéphanie DurandUniversité Clermont Auvergne, INRAE, UNH, Plateforme d'Exploration du Métabolisme, MetaboHUB Clermont, F63122 Saint-Genès Champanelle, Clermont-Ferrand, France.ORCID http://orcid.org/0000-0002-9250-5537
Estelle Pujos-GuillotUniversité Clermont Auvergne, INRAE, UNH, Plateforme d'Exploration du Métabolisme, MetaboHUB Clermont, F63122 Saint-Genès Champanelle, Clermont-Ferrand, France.ORCID http://orcid.org/0000-0002-4693-5712
Julien BoccardSchool of Pharmaceutical Sciences, University of Geneva, Geneva, Switzerland.ORCID http://orcid.org/0000-0001-5913-9566

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAssessing batch correction methods remains a major challenge in metabolomics, as no consensus currently exists for a generic and reliable evaluation strategy. Given the strong influence of batch effects on downstream statistical analyses, establishing a robust framework for their assessment is crucial to ensure result reproducibility and validity.

methodsThis study presents a comprehensive workflow that combines innovative numerical indicators and diagnostic plots to assess multiple dimensions of batch correction performance. It relies on a newly developed indicator, the Batch Conformity Index (BCI), a multivariate, covariance-aware metric quantifying within- and between-batch variability. Complementary visualization tools, including single and multiblock factorization methods, hierarchical clustering and convex hull representations, provide interpretable global diagnostics. These are complemented by compound-level analyses employing classical univariate metrics such as the coefficient of variation, and intra/inter-batch dispersion indices. The workflow also integrates chemistry-based validation via isotopic ratio consistency to ensure that corrections preserve true biochemical information, enabling the detection of potential overfitting or overcorrection.

resultsThe benefits offered by the proposed strategy were illustrated by comparing two widely used correction methods, i.e. LOESS and ComBat, applied to a large-scale serum metabolomics dataset. The results highlighted the complementary strengths and limitations of each method, successfully captured by the proposed workflow, thus providing an objective and interpretable basis for method evaluation.

conclusionThe developed framework offers a unified strategy for evaluating batch correction reliability across multivariate, univariate, and chemical dimensions, representing a significant step toward standardized and reproducible metabolomics data harmonization.

Indexed as

MetabolomicsMultivariate AnalysisReproducibility of ResultsWorkflowBatch correctionReproducibilityWorkflow

Identifiers

PMID42493665
PMCPMC13395890

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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.