Evidence map›Paper›PMID 33736604›Full record

ArticleBMC bioinformatics2021

Statistical integration of two omics datasets using GO2PLS.

Zhujie Gu, Said El Bouhaddani, Jiayi Pei, Jeanine Houwing-Duistermaat, Hae-Won Uh

Abstract read
In one paragraph

Article in BMC bioinformatics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Zhujie GuDepartment of Data Science and Biostatistics, UMC Utrecht, div. Julius Centre, Huispost Str. 6.131, 3508 GA, Utrecht, The Netherlands. z.gu@umcutrecht.nl.ORCID http://orcid.org/0000-0001-7675-8000
Said El BouhaddaniDepartment of Data Science and Biostatistics, UMC Utrecht, div. Julius Centre, Huispost Str. 6.131, 3508 GA, Utrecht, The Netherlands.
Jiayi PeiDepartment of Cardiology, UMC Utrecht, Huispost Str. 6.131, 3508 GA, Utrecht, The Netherlands.
Jeanine Houwing-DuistermaatDepartment of Data Science and Biostatistics, UMC Utrecht, div. Julius Centre, Huispost Str. 6.131, 3508 GA, Utrecht, The Netherlands.
Hae-Won UhDepartment of Data Science and Biostatistics, UMC Utrecht, div. Julius Centre, Huispost Str. 6.131, 3508 GA, Utrecht, The Netherlands.

Funding

H2020 Marie Sklodowska-Curie Actions 721815Wellcome Trust
6 · The paper itself

Abstract

backgroundNowadays, multiple omics data are measured on the same samples in the belief that these different omics datasets represent various aspects of the underlying biological systems. Integrating these omics datasets will facilitate the understanding of the systems. For this purpose, various methods have been proposed, such as Partial Least Squares (PLS), decomposing two datasets into joint and residual subspaces. Since omics data are heterogeneous, the joint components in PLS will contain variation specific to each dataset. To account for this, Two-way Orthogonal Partial Least Squares (O2PLS) captures the heterogeneity by introducing orthogonal subspaces and better estimates the joint subspaces. However, the latent components spanning the joint subspaces in O2PLS are linear combinations of all variables, while it might be of interest to identify a small subset relevant to the research question. To obtain sparsity, we extend O2PLS to Group Sparse O2PLS (GO2PLS) that utilizes biological information on group structures among variables and performs group selection in the joint subspace.

resultsThe simulation study showed that introducing sparsity improved the feature selection performance. Furthermore, incorporating group structures increased robustness of the feature selection procedure. GO2PLS performed optimally in terms of accuracy of joint score estimation, joint loading estimation, and feature selection. We applied GO2PLS to datasets from two studies: TwinsUK (a population study) and CVON-DOSIS (a small case-control study). In the first, we incorporated biological information on the group structures of the methylation CpG sites when integrating the methylation dataset with the IgG glycomics data. The targeted genes of the selected methylation groups turned out to be relevant to the immune system, in which the IgG glycans play important roles. In the second, we selected regulatory regions and transcripts that explained the covariance between regulomics and transcriptomics data. The corresponding genes of the selected features appeared to be relevant to heart muscle disease.

conclusionsGO2PLS integrates two omics datasets to help understand the underlying system that involves both omics levels. It incorporates external group information and performs group selection, resulting in a small subset of features that best explain the relationship between two omics datasets for better interpretability.

Indexed as

Computational BiologyGenomicsCase-Control StudiesLeast-Squares AnalysisDimension reductionFeature selectionGroup structureIntegration of Omics dataO2PLS

Identifiers

PMID33736604
PMCPMC7977326

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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.