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Comparing the performance of linear and nonlinear principal components in the context of high-dimensional genomic data integration

Author

Listed:
  • Islam Shofiqul
  • Anand Sonia
  • Thabane Lehana

    (Population Health Research Institute, McMaster University and Hamilton Health Sciences, Hamilton, Ontario, Canada)

  • Hamid Jemila
  • Beyene Joseph

    (Department of Medicine, McMaster University, 1280 Main Street West, Hamilton, Ontario L8S 4K1, Canada)

Abstract

Linear principal component analysis (PCA) is a widely used approach to reduce the dimension of gene or miRNA expression data sets. This method relies on the linearity assumption, which often fails to capture the patterns and relationships inherent in the data. Thus, a nonlinear approach such as kernel PCA might be optimal. We develop a copula-based simulation algorithm that takes into account the degree of dependence and nonlinearity observed in these data sets. Using this algorithm, we conduct an extensive simulation to compare the performance of linear and kernel principal component analysis methods towards data integration and death classification. We also compare these methods using a real data set with gene and miRNA expression of lung cancer patients. First few kernel principal components show poor performance compared to the linear principal components in this occasion. Reducing dimensions using linear PCA and a logistic regression model for classification seems to be adequate for this purpose. Integrating information from multiple data sets using either of these two approaches leads to an improved classification accuracy for the outcome.

Suggested Citation

  • Islam Shofiqul & Anand Sonia & Thabane Lehana & Hamid Jemila & Beyene Joseph, 2017. "Comparing the performance of linear and nonlinear principal components in the context of high-dimensional genomic data integration," Statistical Applications in Genetics and Molecular Biology, De Gruyter, vol. 16(3), pages 199-216, August.
  • Handle: RePEc:bpj:sagmbi:v:16:y:2017:i:3:p:199-216:n:3
    DOI: 10.1515/sagmb-2016-0066
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    References listed on IDEAS

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