# Probabilistic partial least squares model: Identifiability, estimation   and application

**Authors:** Said el Bouhaddani, Hae-Won Uh, Caroline Hayward, Geurt Jongbloed,, Jeanine Houwing-Duistermaat

arXiv: 1706.03597 · 2021-03-26

## TL;DR

This paper introduces Probabilistic PLS (PPLS), a new model that ensures parameter identifiability, provides a statistical inference framework, and performs well in high-dimensional, non-normal data scenarios, demonstrated through simulations and real data.

## Contribution

The paper develops a probabilistic formulation of PLS with identifiable parameters and an EM algorithm for estimation, addressing limitations of traditional PLS methods.

## Key findings

- PPLS parameters are identifiable up to sign.
- Estimates are robust against non-normality.
- Method performs well in high-dimensional settings.

## 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.

## Full text

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## Figures

17 figures with captions in the complete paper: https://tomesphere.com/paper/1706.03597/full.md

## References

30 references — full list in the complete paper: https://tomesphere.com/paper/1706.03597/full.md

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Source: https://tomesphere.com/paper/1706.03597