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High dimensional classification with combined adaptive sparse PLS and logistic regression.
Durif, Ghislain; Modolo, Laurent; Michaelsson, Jakob; Mold, Jeff E; Lambert-Lacroix, Sophie; Picard, Franck.
Afiliação
  • Durif G; LBBE, UMR CNRS 5558, Université Lyon 1, F-69622 Villeurbanne, France.
  • Modolo L; Univ. Grenoble Alpes, Inria, CNRS, Grenoble INP, LJK, F-38000 Grenoble, France.
  • Michaelsson J; LBBE, UMR CNRS 5558, Université Lyon 1, F-69622 Villeurbanne, France.
  • Mold JE; LBMC UMR 5239 CNRS/ENS Lyon, F-69007 Lyon, France.
  • Lambert-Lacroix S; Department of Cell and Molecular Biology, Karolinska Institutet, Stockholm, Sweden.
  • Picard F; Department of Cell and Molecular Biology, Karolinska Institutet, Stockholm, Sweden.
Bioinformatics ; 34(3): 485-493, 2018 02 01.
Article em En | MEDLINE | ID: mdl-28968879
ABSTRACT
Motivation The high dimensionality of genomic data calls for the development of specific classification methodologies, especially to prevent over-optimistic predictions. This challenge can be tackled by compression and variable selection, which combined constitute a powerful framework for classification, as well as data visualization and interpretation. However, current proposed combinations lead to unstable and non convergent methods due to inappropriate computational frameworks. We hereby propose a computationally stable and convergent approach for classification in high dimensional based on sparse Partial Least Squares (sparse PLS).

Results:

We start by proposing a new solution for the sparse PLS problem that is based on proximal operators for the case of univariate responses. Then we develop an adaptive version of the sparse PLS for classification, called logit-SPLS, which combines iterative optimization of logistic regression and sparse PLS to ensure computational convergence and stability. Our results are confirmed on synthetic and experimental data. In particular, we show how crucial convergence and stability can be when cross-validation is involved for calibration purposes. Using gene expression data, we explore the prediction of breast cancer relapse. We also propose a multicategorial version of our method, used to predict cell-types based on single-cell expression data. Availability and implementation Our approach is implemented in the plsgenomics R-package. Contact ghislain.durif@inria.fr. Supplementary information Supplementary data are available at Bioinformatics online.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Software / Modelos Logísticos / Análise de Sequência de DNA Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Software / Modelos Logísticos / Análise de Sequência de DNA Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2018 Tipo de documento: Article