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Carel F. W. Peeters

Publications and source records attributed to Carel F. W. Peeters.

At least 19 recordsLinked to original sources

A hybrid GPU/CPU implementation of the average information restricted maximum likelihood algorithm for fitting multivariate linear mixed models

The multivariate linear mixed model combined with restricted maximum likelihood estimation of (co)variance components and solving the mixed model equations is widely used for the analysis of plant breeding data. Several algorithms for restricted maximum likelihood estimation have been proposed, with the average information algorithm being widely used for its computational efficiency, quadratic rate of convergence, and ability to handle large amounts of parameters. A key reason for the scalability of linear mixed models is the exploitation of sparse matrix techniques. Recently, decreasing costs of high-throughput data collection have led to high-dimensional sets of features characterizing genotypes and environments. A convenient way of using these features is through the use of kernel-based covariance structures. However, while convenient, these kernels typically have dense inverses meaning optimizations based on sparse matrix techniques are not always applicable. For these settings, the introduction of general-purpose computing on graphics processing units brought significant computational advantages for dense linear algebra operations. We present a hybrid GPU/CPU implementation of the average information restricted maximum likelihood algorithm. We eliminate sparse equations using supernodal Cholesky factorization and rely on CUDA GPU acceleration to solve the resulting reduced dense system. We show the significant computational advantages of this approach for fully dense problems, as well as problems with a mix of dense and sparse equations.

stat.CO↗

Perspectives on Latent Factor Indeterminacy and its Implications for Data Representation

The common factor analytic model is related to Helmholtz and Boltzmann machines, can be conceived as a linear autoencoder, or can be thought of as a single-hidden-layer generative neural network. We thus consider it a basal generative representation learner that can be used as a minimal model for studying the foundational characteristics of (deep) generative model architectures. We focus on the fundamental problem of indeterminacy in latent factor projections. This indeterminacy implies that, even when the intrinsic dimension of the latent vector is known, regularity conditions are met, and rotational indeterminacy is resolved, an inherent indefiniteness in the retrieval of causative latent sources remains: they will be uncertain, distributionally deviant, and non-unique. This can have major implications for data representation but remains an elusive issue, even to practitioners and theorists well-versed in the factor model. Moreover, this classic psychometric problem is intricately related to the modern issue of latent variable collapse in the variational autoencoder framework for deep generative modeling. Here, we assess this indeterminacy from various perspectives and show how these are mathematically and conceptually related and we discuss subsequent implications for the Psychometrics, Statistics, and Artificial Intelligence communities. We show that one has latent factor determinacy across all its facets when the feature-dimension grows to infinity. This feeds into an essentially distribution-free estimation approach in the sample case when the number of features grows very large. We conclude, as these are emergent properties at scale, that the factor model is suited for representation learning of very-high-dimensional data.

stat.ML↗

REML implementations of kernel-based genomic prediction models for genotype x environment x management interactions

High-throughput pheno-, geno-, and envirotyping allows characterization of plant genotypes and the trials they are evaluated in, producing different types of data. These different data modalities can be integrated into statistical or machine learning models for genomic prediction in several ways. One commonly used approach within the analysis of multi-environment trial data in plant breeding is to create linear or nonlinear kernels which are subsequently used in linear mixed models (LMMs) to model genotype by environment (G$\times$E) interactions. Current implementations of these kernel-based LMMs present a number of opportunities in terms of methodological extensions. Here we show how these models can be implemented in standard software, allowing direct restricted maximum likelihood (REML) estimation of all parameters. We also further extend the models by combining the kernels with unstructured covariance matrices for three-way interactions in genotype by environment by management (G$\times$E$\times$M) datasets, while simultaneously allowing for environment-specific genetic variances. We show how the models incorporating nonlinear kernels and heterogeneous variances maximize the amount of genetic variance captured by environmental covariables and perform best in prediction settings. We discuss the opportunities regarding models with multiple kernels or kernels obtained after environmental feature selection, as well as the similarities to models regressing phenotypes on latent and observed environmental covariables. Finally, we discuss the flexibility provided by our implementation in terms of modeling complex plant breeding datasets, allowing for straightforward integration of phenomics, enviromics, and genomics.

stat.ME↗

A latent factor approach to hyperspectral time series data for multivariate genomic prediction of grain yield in wheat

High-dimensional time series phenotypic data is becoming increasingly common within plant breeding programmes. However, analysing and integrating such data for genetic analysis and genomic prediction remains difficult. Here we show how factor analysis with Procrustes rotation on the genetic correlation matrix of hyperspectral secondary phenotype data can help in extracting relevant features for within-trial prediction. We use a subset of Centro Internacional de Mejoramiento de Maíz y Trigo (CIMMYT) elite yield wheat trial of 2014-2015, consisting of 1,033 genotypes. These were measured across three irrigation treatments at several timepoints during the season, using manned airplane flights with hyperspectral sensors capturing 62 bands in the spectrum of 385-850 nm. We perform multivariate genomic prediction using latent variables to improve within-trial genomic predictive ability (PA) of wheat grain yield within three distinct watering treatments. By integrating latent variables of the hyperspectral data in a multivariate genomic prediction model, we are able to achieve an absolute gain of .1 to .3 (on the correlation scale) in PA compared to univariate genomic prediction. Furthermore, we show which timepoints within a trial are important and how these relate to plant growth stages. This paper showcases how domain knowledge and data-driven approaches can be combined to increase PA and gain new insights from sensor data of high-throughput phenotyping platforms.

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Improving Genomic Prediction using High-dimensional Secondary Phenotypes: the Genetic Latent Factor Approach

Decreasing costs and new technologies have led to an increase in the amount of data available to plant breeding programs. High-throughput phenotyping (HTP) platforms routinely generate high-dimensional datasets of secondary features that may be used to improve genomic prediction accuracy. However, integration of these data comes with challenges such as multicollinearity, parameter estimation in $p > n$ settings, and the computational complexity of many standard approaches. Several methods have emerged to analyze such data, but interpretation of model parameters often remains challenging. We propose genetic latent factor best linear unbiased prediction (glfBLUP), a prediction pipeline that reduces the dimensionality of the original secondary HTP data using generative factor analysis. In short, glfBLUP uses redundancy filtered and regularized genetic and residual correlation matrices to fit a maximum likelihood factor model and estimate genetic latent factor scores. These latent factors are subsequently used in multi-trait genomic prediction. Our approach performs better than alternatives in extensive simulations and a real-world application, while producing easily interpretable and biologically relevant parameters. We discuss several possible extensions and highlight glfBLUP as the basis for a flexible and modular multi-trait genomic prediction framework.

stat.ME↗

Semi-supervised empirical Bayes group-regularized factor regression

The features in high dimensional biomedical prediction problems are often well described with lower dimensional manifolds. An example is genes that are organised in smaller functional networks. The outcome can then be described with the factor regression model. A benefit of the factor model is that is allows for straightforward inclusion of unlabeled observations in the estimation of the model, i.e., semi-supervised learning. In addition, the high dimensional features in biomedical prediction problems are often well characterised. Examples are genes, for which annotation is available, and metabolites with $p$-values from a previous study available. In this paper, the extra information on the features is included in the prior model for the features. The extra information is weighted and included in the estimation through empirical Bayes, with Variational approximations to speed up the computation. The method is demonstrated in simulations and two applications. One application considers influenza vaccine efficacy prediction based on microarray data. The second application predictions oral cancer metastatsis from RNAseq data.

stat.ME↗

rags2ridges: A One-Stop-Shop for Graphical Modeling of High-Dimensional Precision Matrices

A graphical model is an undirected network representing the conditional independence properties between random variables. Graphical modeling has become part and parcel of systems or network approaches to multivariate data, in particular when the variable dimension exceeds the observation dimension. rags2ridges is an R package for graphical modeling of high-dimensional precision matrices. It provides a modular framework for the extraction, visualization, and analysis of Gaussian graphical models from high-dimensional data. Moreover, it can handle the incorporation of prior information as well as multiple heterogeneous data classes. As such, it provides a one-stop-shop for graphical modeling of high-dimensional precision matrices. The functionality of the package is illustrated with an example dataset pertaining to blood-based metabolite measurements in persons suffering from Alzheimer's Disease.

stat.ME↗

Targeted Fused Ridge Estimation of Inverse Covariance Matrices from Multiple High-Dimensional Data Classes

We consider the problem of jointly estimating multiple inverse covariance matrices from high-dimensional data consisting of distinct classes. An $\ell_2$-penalized maximum likelihood approach is employed. The suggested approach is flexible and generic, incorporating several other $\ell_2$-penalized estimators as special cases. In addition, the approach allows specification of target matrices through which prior knowledge may be incorporated and which can stabilize the estimation procedure in high-dimensional settings. The result is a targeted fused ridge estimator that is of use when the precision matrices of the constituent classes are believed to chiefly share the same structure while potentially differing in a number of locations of interest. It has many applications in (multi)factorial study designs. We focus on the graphical interpretation of precision matrices with the proposed estimator then serving as a basis for integrative or meta-analytic Gaussian graphical modeling. Situations are considered in which the classes are defined by data sets and subtypes of diseases. The performance of the proposed estimator in the graphical modeling setting is assessed through extensive simulation experiments. Its practical usability is illustrated by the differential network modeling of 12 large-scale gene expression data sets of diffuse large B-cell lymphoma subtypes. The estimator and its related procedures are incorporated into the R-package rags2ridges.

stat.ME↗

Social Network Analysis of Corruption Structures: Adjacency Matrices Supporting the Visualization and Quantification of Layeredness

Often, corruption is described as taking place within or supported by a network: A collection of individuals structured in such a way as to enable the transaction of bribes for favors. Surprisingly, despite the network nomenclature, corruption is rarely analyzed from the network perspective using the tools of network science. Here, we will argue that analyzing corruption from the perspective of network science is beneficial to its understanding. In passing this chapter, a contribution to the Liber Amicorum in honor of Leo Huberts, then gives a very short introduction into social network analysis.

physics.soc-ph↗

Rotational Uniqueness Conditions Under Oblique Factor Correlation Metric

In an addendum to his seminal 1969 article Jöreskog stated two sets of conditions for rotational identification of the oblique factor solution under utilization of fixed zero elements in the factor loadings matrix. These condition sets, formulated under factor correlation and factor covariance metrics, respectively, were claimed to be equivalent and to lead to global rotational uniqueness of the factor solution. It is shown here that the conditions for the oblique factor correlation structure need to be amended for global rotational uniqueness, and hence, that the condition sets are not equivalent in terms of unicity of the solution.

math.ST↗

A Note on a Simple and Practical Randomized Response Framework for Eliciting Sensitive Dichotomous & Quantitative Information

Many issues of interest to social scientists and policymakers are of a sensitive nature in the sense that they are intrusive, stigmatizing or incriminating to the respondent. This results in refusals to cooperate or evasive cooperation in studies using self-reports. In a seminal article Warner proposed to curb this problem by generating an artificial variability in responses to inoculate the individual meaning of answers to sensitive questions. This procedure was further developed and extended, and came to be known as the randomized response (RR) technique. Here, we propose a unified treatment for eliciting sensitive binary as well as quantitative information with RR based on a model where the inoculating elements are provided for by the randomization device. The procedure is simple and we will argue that its implementation in a computer-assisted setting may have superior practical capabilities.

stat.AP↗

Stable prediction with radiomics data

Motivation: Radiomics refers to the high-throughput mining of quantitative features from radiographic images. It is a promising field in that it may provide a non-invasive solution for screening and classification. Standard machine learning classification and feature selection techniques, however, tend to display inferior performance in terms of (the stability of) predictive performance. This is due to the heavy multicollinearity present in radiomic data. We set out to provide an easy-to-use approach that deals with this problem. Results: We developed a four-step approach that projects the original high-dimensional feature space onto a lower-dimensional latent-feature space, while retaining most of the covariation in the data. It consists of (i) penalized maximum likelihood estimation of a redundancy filtered correlation matrix. The resulting matrix (ii) is the input for a maximum likelihood factor analysis procedure. This two-stage maximum-likelihood approach can be used to (iii) produce a compact set of stable features that (iv) can be directly used in any (regression-based) classifier or predictor. It outperforms other classification (and feature selection) techniques in both external and internal validation settings regarding survival in squamous cell cancers.

stat.ML↗

Adaptive group-regularized logistic elastic net regression

In high-dimensional data settings, additional information on the features is often available. Examples of such external information in omics research are: (a) p-values from a previous study, (b) a summary of prior information, and (c) omics annotation. The inclusion of this information in the analysis may enhance classification performance and feature selection, but is not straightforward in the standard regression setting. As a solution to this problem, we propose a group-regularized (logistic) elastic net regression method, where each penalty parameter corresponds to a group of features based on the external information. The method, termed gren, makes use of the Bayesian formulation of logistic elastic net regression to estimate both the model and penalty parameters in an approximate empirical-variational Bayes framework. Simulations and an application to a colon cancer microRNA study show that, if the partitioning of the features is informative, classification performance and feature selection are indeed enhanced.

stat.ME↗

Inequality Constrained Multilevel Models

Multilevel or hierarchical data structures can occur in many areas of research, including economics, psychology, sociology, agriculture, medicine, and public health. Over the last 25 years, there has been increasing interest in developing suitable techniques for the statistical analysis of multilevel data, and this has resulted in a broad class of models known under the generic name of multilevel models. Generally, multilevel models are useful for exploring how relationships vary across higher-level units taking into account the within and between cluster variations. Research scientists often have substantive theories in mind when evaluating data with statistical models. Substantive theories often involve inequality constraints among the parameters to translate a theory into a model. This chapter shows how the inequality constrained multilevel linear model can be given a Bayesian formulation, how the model parameters can be estimated using a so-called augmented Gibbs sampler, and how posterior probabilities can be computed to assist the researcher in model selection.

stat.ME↗

Blood-based metabolic signatures in Alzheimer's disease

Introduction: Identification of blood-based metabolic changes might provide early and easy-to-obtain biomarkers. Methods: We included 127 AD patients and 121 controls with CSF-biomarker-confirmed diagnosis (cut-off tau/A$β_{42}$: 0.52). Mass spectrometry platforms determined the concentrations of 53 amine, 22 organic acid, 120 lipid, and 40 oxidative stress compounds. Multiple signatures were assessed: differential expression (nested linear models), classification (logistic regression), and regulatory (network extraction). Results: Twenty-six metabolites were differentially expressed. Metabolites improved the classification performance of clinical variables from 74% to 79%. Network models identified 5 hubs of metabolic dysregulation: Tyrosine, glycylglycine, glutamine, lysophosphatic acid C18:2 and platelet activating factor C16:0. The metabolite network for APOE $ε$4 negative AD patients was less cohesive compared to the network for APOE $ε$4 positive AD patients. Discussion: Multiple signatures point to various promising peripheral markers for further validation. The network differences in AD patients according to APOE genotype may reflect different pathways to AD.

q-bio.NC↗

Detecting functional decline from normal ageing to dementia: development and validation of a short version of the Amsterdam IADL Questionnaire

INTRODUCTION: Detecting functional decline from normal ageing to dementia is relevant for diagnostic and prognostic purposes. Therefore, the Amsterdam IADL Questionnaire (A-IADL-Q) was developed: a 70-item proxy-based tool with good psychometric properties. We aimed to design a short version whilst preserving its psychometric quality. METHODS: Study partners of subjects (n=1355), ranging from cognitively normal to dementia subjects, completed the original A-IADL-Q. We selected the short version items using a stepwise procedure combining missing data, Item Response Theory and input from respondents and experts. We investigated internal consistency of the short version as well as concordance with the original version. To assess its construct validity, we additionally investigated concordance between the short version and the Mini-Mental State Examination (MMSE) and Disability Assessment for Dementia (DAD). Lastly, we investigated differences in IADL scores between diagnostic groups across the dementia spectrum. RESULTS: We selected 30 items covering the entire spectrum of IADL functioning. Internal consistency (.98) and concordance with the original version (.97) were very high. Concordance with the MMSE (.72) and DAD (.87) scores was high. IADL impairment scores increased across the spectrum from normal cognition to dementia. DISCUSSION: The A-IADL-Q Short Version (A-IADL-Q-SV) consists of 30 items. The A-IADL-Q-SV has maintained the psychometric quality of the original A-IADL-Q. As such, it is a concise measure of functional decline.

q-bio.NC↗

Pathophysiological Domains Underlying the Metabolic Syndrome: An Alternative Factor Analytic Strategy

Purpose: Factor analysis (FA) has become part and parcel in metabolic syndrome (MBS) research. Both exploration- and confirmation-driven factor analyzes are rampant. However, factor analytic results on MBS differ widely. A situation that is at least in part attributable to misapplication of FA. Here, our purpose is (i) to review factor analytic efforts in the study of MBS with emphasis on misusage of the FA model and (ii) to propose an alternative factor analytic strategy. Methods: The proposed factor analytic strategy consists of four steps and confronts weaknesses in application of the FA model. At its heart lies the explicit separation of dimensionality and pattern selection as well as the direct evaluation of competing inequality-constrained loading patterns. A high-profile MBS data set with anthropometric measurements on overweight children and adolescents is reanalyzed using this strategy. Results: The reanalysis implied a more parsimonious constellation of pathophysiological domains underlying phenotypic expressions of MBS than the original analysis (and many other analyzes). The results emphasize correlated factors of impaired glucose metabolism and impaired lipid metabolism. Conclusions: Pathophysiological domains underlying phenotypic expressions of MBS included in the analysis are driven by multiple interrelated metabolic impairments. These findings indirectly point to the possible existence of a multifactorial aetiology.

stat.AP↗

The Spectral Condition Number Plot for Regularization Parameter Determination

Many modern statistical applications ask for the estimation of a covariance (or precision) matrix in settings where the number of variables is larger than the number of observations. There exists a broad class of ridge-type estimators that employs regularization to cope with the subsequent singularity of the sample covariance matrix. These estimators depend on a penalty parameter and choosing its value can be hard, in terms of being computationally unfeasible or tenable only for a restricted set of ridge-type estimators. Here we introduce a simple graphical tool, the spectral condition number plot, for informed heuristic penalty parameter selection. The proposed tool is computationally friendly and can be employed for the full class of ridge-type covariance (precision) estimators.

stat.CO↗