Evidence map›Paper›PMID 41444512›Full record

ArticleBMC bioinformatics2025

Statistical modelling of an outcome variable with integrated multi-omics.

He Li, Zander Gu, Said El Bouhaddani, Jeanine Houwing-Duistermaat

Abstract read
In one paragraph

Article in BMC bioinformatics, 2025. 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

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2 · The registry

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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.

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

He Li *Department of Mathematics, Radboud University, Heyendaalseweg, 6525 AJ, Nijmegen, Gelderland, The Netherlands. he.li@ru.nl.ORCID http://orcid.org/0009-0000-7288-3330
Zander Gu *Medical Research Council Biostatistics Unit, University of Cambridge, Robinson Way, Cambridge, Cambridgeshire, CB2 0SR, UK.ORCID http://orcid.org/0000-0001-7675-8000
Said El BouhaddaniJulius Centre, UMC Utrecht, Universiteitsweg, 3584 CG, Utrecht, Utrecht, The Netherlands.ORCID http://orcid.org/0000-0002-2279-4337
Jeanine Houwing-DuistermaatDepartment of Mathematics, Radboud University, Heyendaalseweg, 6525 AJ, Nijmegen, Gelderland, The Netherlands.ORCID http://orcid.org/0000-0002-4505-7137

Funding

ERA-Net E-Rare JTC 2018 (MSA-omics) 40-44000-98-2006 / 90030376507European Union's Horizon 2020 research and innovation programme (IMforFUTURE) 721815Wellcome Trust
6 · The paper itself

Abstract

backgroundIn studies that aim to model the relationship between an outcome variable and multiple omics datasets, it is often desirable to reduce the dimensionality of these datasets or to represent one omics dataset in terms of another. Several approaches exist for this purpose, including univariate methods such as polygenic scores, and multivariate methods. Multivariate approaches offer advantages by producing lower-dimensional integrative scores, capturing joint structures across datasets, and filtering out dataset-specific noise. In this paper, we describe one univariate and two multivariate methods, and evaluate their performance through simulations involving two correlated multivariate normally distributed omics datasets, as well as a combination of one multivariate normal and one fixed categorical dataset.

resultsWe assess method performance using the root mean squared error (RMSE) when modelling the outcome variable as a function of the reduced omics representations. Multivariate methods generally perform well, particularly when a slightly higher number of components is used for integration. They outperform the univariate method in scenarios involving two normally distributed omics datasets and perform comparably in settings with one normal and one categorical dataset. In real data applications, including two metabolomics datasets from TwinsUK and a metabolomics-genetic dataset from ORCADES, all methods show similar performance in modelling body mass index.

conclusionsMultivariate methods provide a valuable framework for summarizing multi-omics datasets into low-dimensional components suitable for outcome modelling. Even in the presence of non-normal data, these methods offer a promising alternative to high-dimensional univariate approaches.

Indexed as

Computational BiologyGenomicsMetabolomicsModels, StatisticalBody Mass IndexHumansMultiomicsMultivariate AnalysisLatent variablesLow-dimensional representationMetabolomicsMultivariate analysisPolygenic score

Identifiers

PMID41444512
PMCPMC12859906

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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.