Probabilistic partial least squares model

Identifiability, estimation and application

Journal Article (2018)
Author(s)

S. el Bouhaddani (Leiden University Medical Center)

Hae-Won Uh (Leiden University Medical Center, University Medical Center Utrecht)

Caroline Hayward (The University of Edinburgh)

Geurt Jongbloed (TU Delft - Delft Institute of Applied Mathematics)

Jeanine Houwing-Duistermaat (Leiden University Medical Center, University of Leeds)

Department
Delft Institute of Applied Mathematics
Copyright
© 2018 S. el Bouhaddani, Hae Won Uh, Caroline Hayward, G. Jongbloed, Jeanine Houwing-Duistermaat
DOI related publication
https://doi.org/10.1016/j.jmva.2018.05.009
More Info
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Publication Year
2018
Language
English
Copyright
© 2018 S. el Bouhaddani, Hae Won Uh, Caroline Hayward, G. Jongbloed, Jeanine Houwing-Duistermaat
Department
Delft Institute of Applied Mathematics
Bibliographical Note
Accepted Author Manuscript@en
Volume number
167
Pages (from-to)
331-346
Reuse Rights

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Abstract

With a rapid increase in volume and complexity of data sets, there is a need for methods that can extract useful information, for example the relationship between two data sets measured for the same persons. The Partial Least Squares (PLS) method can be used for this dimension reduction task. Within life sciences, results across studies are compared and combined. Therefore, parameters need to be identifiable, which is not the case for PLS. In addition, PLS is an algorithm, while epidemiological study designs are often outcome-dependent and methods to analyze such data require a probabilistic formulation. Moreover, a probabilistic model provides a statistical framework for inference. To address these issues, we develop Probabilistic PLS (PPLS). We derive maximum likelihood estimators that satisfy the identifiability conditions by using an EM algorithm with a constrained optimization in the M step. We show that the PPLS parameters are identifiable up to sign. A simulation study is conducted to study the performance of PPLS compared to existing methods. The PPLS estimates performed well in various scenarios, even in high dimensions. Most notably, the estimates seem to be robust against departures from normality. To illustrate our method, we applied it to IgG glycan data from two cohorts. Our PPLS model provided insight as well as interpretable results across the two cohorts.

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