Evaluation of the effect of chance correlations on variable selection using Partial Least Squares-Discriminant Analysis.

Fecha de publicación:

Autores de IIS La Fe

  • Justo Javier Escobar Cubiella

    Autor

  • Máximo Vento Torres

    Autor

  • Guillermo Quintas Soriano

    Autor

Participantes ajenos a IIS La Fe

  • Pérez-Guaita D
  • de la Guardia M
  • Ferrer A

Grupos

Abstract

Variable subset selection is often mandatory in high throughput metabolomics and proteomics. However, depending on the variable to sample ratio there is a significant susceptibility of variable selection towards chance correlations. The evaluation of the predictive capabilities of PLSDA models estimated by cross-validation after feature selection provides overly optimistic results if the selection is performed on the entire set and no external validation set is available. In this work, a simulation of the statistical null hypothesis is proposed to test whether the discrimination capability of a PLSDA model after variable selection estimated by cross-validation is statistically higher than that attributed to the presence of chance correlations in the original data set. Statistical significance of PLSDA CV-figures of merit obtained after variable selection is expressed by means of p-values calculated by using a permutation test that included the variable selection step. The reliability of the approach is evaluated using two variable selection methods on experimental and simulated data sets with and without induced class differences. The proposed approach can be considered as a useful tool when no external validation set is available and provides a straightforward way to evaluate differences between variable selection methods.

Datos de la publicación

ISSN/ISSNe:
0039-9140, 1873-3573

Talanta  ELSEVIER SCIENCE BV

Tipo:
Article
Páginas:
835-840
PubMed:
24148482
Factor de Impacto:
1,200 SCImago

Citas Recibidas en Web of Science: 21

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Keywords

  • Chance correlations, Metabolomics, Partial Least Squares-Discriminant Analysis (PLSDA), Variable selection

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