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Martelli, Pier Luigi (Ed.)Abstract MotivationThere is a growing interest in longitudinal omics data paired with some longitudinal clinical outcome. Given a large set of continuous omics variables and some continuous clinical outcome, each measured for a few subjects at only a few time points, we seek to identify those variables that co-vary over time with the outcome. To motivate this problem we study a dataset with hundreds of urinary metabolites along with Tuberculosis mycobacterial load as our clinical outcome, with the objective of identifying potential biomarkers for disease progression. For such data clinicians usually apply simple linear mixed effects models which often lack power given the low number of replicates and time points. We propose a penalized regression approach on the first differences of the data that extends the lasso + Laplacian method [Li and Li (Network-constrained regularization and variable selection for analysis of genomic data. Bioinformatics 2008;24:1175–82.)] to a longitudinal group lasso + Laplacian approach. Our method, PROLONG, leverages the first differences of the data to increase power by pairing the consecutive time points. The Laplacian penalty incorporates the dependence structure of the variables, and the group lasso penalty induces sparsity while grouping together all contemporaneous and lag terms for each omic variable in the model. ResultsWith an automated selection of model hyper-parameters, PROLONG correctly selects target metabolites with high specificity and sensitivity across a wide range of scenarios. PROLONG selects a set of metabolites from the real data that includes interesting targets identified during EDA. Availability and implementationAn R package implementing described methods called “prolong” is available at https://github.com/stevebroll/prolong. Code snapshot available at 10.5281/zenodo.14804245.more » « lessFree, publicly-accessible full text available March 29, 2026
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Free, publicly-accessible full text available March 26, 2026
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Free, publicly-accessible full text available February 18, 2026
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The significantly increasing number of vehicles brings convenience to daily life while also introducing significant challenges to the transportation network and air pollution. It has been proved that platooning/clustering-based driving can significantly reduce road congestion and exhaust emissions and improve road capacity and energy efficiency. This paper aims to improve the stability of vehicle clustering to enhance the lifetime of cooperative driving. Specifically, we use a Graph Neural Network (GNN) model to learn effective node representations, which can help aggregate vehicles with similar patterns into stable clusters. To the best of our knowledge, this is the first generalized learnable GNN-based model for vehicular ad hoc network clustering. In addition, our centralized approach makes full use of the ubiquitous presence of the base stations and edge clouds. It is noted that a base station has a vantage view of the vehicle distribution within the coverage area as compared to distributed clustering approaches. Specifically, eNodeB-assisted clustering can greatly reduce the control message overhead during the cluster formation and offload to eNodeB the complex computations required for machine learning algorithms. We evaluated the performance of the proposed clustering algorithms on the open-source highD dataset. The experiment results demonstrate that the average cluster lifetime and cluster efficiency of our GNN-based clustering algorithm outperforms state-of-the-art baselines.more » « less
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