Multiblock variable influence on orthogonal projections (MB-VIOP) for enhanced interpretation of total, global, local and unique variations in OnPLS models.

Feature selection Latent variable interpretation MB-VIOP Multiblock variable selection OnPLS VIP Variable importance in multiblock regression Variable influence on projection

Journal

BMC bioinformatics
ISSN: 1471-2105
Titre abrégé: BMC Bioinformatics
Pays: England
ID NLM: 100965194

Informations de publication

Date de publication:
03 Apr 2021
Historique:
received: 16 07 2020
accepted: 10 02 2021
entrez: 4 4 2021
pubmed: 5 4 2021
medline: 10 4 2021
Statut: epublish

Résumé

For multivariate data analysis involving only two input matrices (e.g., X and Y), the previously published methods for variable influence on projection (e.g., VIP A method for variable selection in multiblock analysis, called multiblock variable influence on orthogonal projections (MB-VIOP) is explained in this paper. MB-VIOP is a model based variable selection method that uses the data matrices, the scores and the normalized loadings of an OnPLS model in order to sort the input variables of more than two data matrices according to their importance for both simplification and interpretation of the total multiblock model, and also of the unique, local and global model components separately. MB-VIOP has been tested using three datasets: a synthetic four-block dataset, a real three-block omics dataset related to plant sciences, and a real six-block dataset related to the food industry. We provide evidence for the usefulness and reliability of MB-VIOP by means of three examples (one synthetic and two real-world cases). MB-VIOP assesses in a trustable and efficient way the importance of both isolated and ranges of variables in any type of data. MB-VIOP connects the input variables of different data matrices according to their relevance for the interpretation of each latent variable, yielding enhanced interpretability for each OnPLS model component. Besides, MB-VIOP can deal with strong overlapping of types of variation, as well as with many data blocks with very different dimensionality. The ability of MB-VIOP for generating dimensionality reduced models with high interpretability makes this method ideal for big data mining, multi-omics data integration and any study that requires exploration and interpretation of large streams of data.

Sections du résumé

BACKGROUND BACKGROUND
For multivariate data analysis involving only two input matrices (e.g., X and Y), the previously published methods for variable influence on projection (e.g., VIP
RESULTS RESULTS
A method for variable selection in multiblock analysis, called multiblock variable influence on orthogonal projections (MB-VIOP) is explained in this paper. MB-VIOP is a model based variable selection method that uses the data matrices, the scores and the normalized loadings of an OnPLS model in order to sort the input variables of more than two data matrices according to their importance for both simplification and interpretation of the total multiblock model, and also of the unique, local and global model components separately. MB-VIOP has been tested using three datasets: a synthetic four-block dataset, a real three-block omics dataset related to plant sciences, and a real six-block dataset related to the food industry.
CONCLUSIONS CONCLUSIONS
We provide evidence for the usefulness and reliability of MB-VIOP by means of three examples (one synthetic and two real-world cases). MB-VIOP assesses in a trustable and efficient way the importance of both isolated and ranges of variables in any type of data. MB-VIOP connects the input variables of different data matrices according to their relevance for the interpretation of each latent variable, yielding enhanced interpretability for each OnPLS model component. Besides, MB-VIOP can deal with strong overlapping of types of variation, as well as with many data blocks with very different dimensionality. The ability of MB-VIOP for generating dimensionality reduced models with high interpretability makes this method ideal for big data mining, multi-omics data integration and any study that requires exploration and interpretation of large streams of data.

Identifiants

pubmed: 33812384
doi: 10.1186/s12859-021-04015-9
pii: 10.1186/s12859-021-04015-9
pmc: PMC8019512
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

176

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Auteurs

Beatriz Galindo-Prieto (B)

Department of Chemistry, Computational Life Science Cluster (CLiC), Umeå University, Umeå, Sweden. beg4004@med.cornell.edu.
Industrial Doctoral School (IDS), Umeå, Sweden. beg4004@med.cornell.edu.
Department of Engineering Cybernetics (ITK), Norwegian University of Science and Technology (NTNU), Trondheim, Norway. beg4004@med.cornell.edu.
Helen and Robert Appel Alzheimer's Disease Research Institute, Feil Family Brain and Mind Research Institute, Weill Cornell Medicine (WCM), Cornell University, New York, NY, USA. beg4004@med.cornell.edu.

Paul Geladi (P)

Forest Biomaterials and Technology, Swedish University of Agricultural Sciences (SLU), Umeå, Sweden.

Johan Trygg (J)

Department of Chemistry, Computational Life Science Cluster (CLiC), Umeå University, Umeå, Sweden. johan.trygg@umu.se.
Sartorius Corporate Research, Umeå, Sweden. johan.trygg@umu.se.

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