Cited by 9Bioinformatics and Genomic NetworksGene expression and cancer classificationSingle-cell and spatial transcriptomics

Model-based joint visualization of multiple compositional omics datasets

Open access
Hawinkel, Stijn, Bijnens, Luc, Cao, Kim-Anh Lê, Thas, Olivier·2020·NAR Genomics and Bioinformatics

Abstract

Abstract The integration of multiple omics datasets measured on the same samples is a challenging task: data come from heterogeneous sources and vary in signal quality. In addition, some omics data are inherently compositional, e.g. sequence count data. Most integrative methods are limited in their ability to handle covariates, missing values, compositional structure and heteroscedasticity. In this article we introduce a flexible model-based approach to data integration to address these current limitations: COMBI. We combine concepts, such as compositional biplots and log-ratio link functions with latent variable models, and propose an attractive visualization through multiplots to improve interpretation. Using real data examples and simulations, we illustrate and compare our method with other data integration techniques. Our algorithm is available in the R-package combi.

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Crossref · 10.1093/nargab/lqaa050

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  • Complete case analysis, while convenient, results in a decrease in sample size, throws away useful data, is only valid under the MCAR assumption and can otherwise lead to biased estimates.

    “This approach, while convenient, results in a decrease in sample size, throws away useful data, is only valid under the MCAR assumption and can otherwise lead to biased estimates (Fang et al., 2018; Hawinkel et al., 2020).”
  • COMBI's quasi-likelihood estimation approach is robust to missing data values.

    “The quasi-likelihood estimation approach is also robust to missing data values.”
  • Provided that data are missing completely at random (MCAR) or missing at random (MAR), COMBI's quasi-likelihood estimation procedure yields unbiased parameter estimates based on all complete or partial observations.

    “Provided that the data are missing completely at random (MCAR) or missing at random (MAR), the quasi-likelihood estimation procedure yields unbiased parameter estimates based on all (complete or partial) observations.”

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Research works printed but not linked: 1

  1. [37]Argelaguet R., Velten B., Arnol D., Buettner F., Huber W., Stegle O. MOFA: multi-omics factor analysis (MOFA). 2019; R package version 1.0.0.. PMC6010767 29925568

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Authors
Hawinkel, S., Bijnens, L., Cao, K.-A. L., & Thas, O.
Affiliations
  • Ghent University (BE)
  • Janssen (Belgium) (BE)
  • The University of Melbourne (AU)
  • University of Wollongong (AU)
Corresponding author
Hawinkel, Stijn
Venue
NAR Genomics and Bioinformatics
Published
2020-07-21
Volume
2
Issue
3
Pages
lqaa050-lqaa050
ISSN
2631-9268 (ISSN-L)
OpenAlex
W3045412769
Cited by
9
References
41
Citations by year
2025: 2 · 2024: 3 · 2023: 1 · 2022: 1 · 2021: 1 · 2020: 1
FWCI
0.32
Type
journal article
Language
en
Open access
Locations
  • NAR Genomics and Bioinformatics (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • Ghent University Academic Bibliography (Ghent University) (submittedVersion, other-oa)
  • Document Server@UHasselt (UHasselt) (submittedVersion, other-oa)
  • Minerva Access (University of Melbourne) (submittedVersion, cc-by)
Funders
Johnson and Johnson
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bioinformatics and Genomic Networks
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gene expression and cancer classification
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Single-cell and spatial transcriptomics
Keywords
multi-omics integration, compositional data, latent variable models, heteroscedasticity, missing data, covariate adjustment

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