Markus Heinonen1, Olivier Guipaud2, Fabien Milliat2, Valérie Buard2, Béatrice Micheau2, Georges Tarlet2, Marc Benderitter2, Farida Zehraoui2, Florence d'Alché-Buc1. 1. IBISC, Universite d'Évry Val d'Essonne, 23 Boulevard de France, 91025 Évry, France, AMIB, INRIA-Saclay, LRI UMR CNRS 8623, Université Paris Sud, Orsay, France, and Institut de Radioprotection et de Sûreté Nucléaire, LRTE, 92262 Fontenay-aux-roses, France IBISC, Universite d'Évry Val d'Essonne, 23 Boulevard de France, 91025 Évry, France, AMIB, INRIA-Saclay, LRI UMR CNRS 8623, Université Paris Sud, Orsay, France, and Institut de Radioprotection et de Sûreté Nucléaire, LRTE, 92262 Fontenay-aux-roses, France. 2. IBISC, Universite d'Évry Val d'Essonne, 23 Boulevard de France, 91025 Évry, France, AMIB, INRIA-Saclay, LRI UMR CNRS 8623, Université Paris Sud, Orsay, France, and Institut de Radioprotection et de Sûreté Nucléaire, LRTE, 92262 Fontenay-aux-roses, France.
Abstract
MOTIVATION: Identifying the set of genes differentially expressed along time is an important task in two-sample time course experiments. Furthermore, estimating at which time periods the differential expression is present can provide additional insight into temporal gene functions. The current differential detection methods are designed to detect difference along observation time intervals or on single measurement points, warranting dense measurements along time to characterize the full temporal differential expression patterns. RESULTS: We propose a novel Bayesian likelihood ratio test to estimate the differential expression time periods. Applying the ratio test to systems of genes provides the temporal response timings and durations of gene expression to a biological condition. We introduce a novel non-stationary Gaussian process as the underlying expression model, with major improvements on model fitness on perturbation and stress experiments. The method is robust to uneven or sparse measurements along time. We assess the performance of the method on realistically simulated dataset and compare against state-of-the-art methods. We additionally apply the method to the analysis of primary human endothelial cells under an ionizing radiation stress to study the transcriptional perturbations over 283 measured genes in an attempt to better understand the role of endothelium in both normal and cancer tissues during radiotherapy. As a result, using the cascade of differential expression periods, domain literature and gene enrichment analysis, we gain insights into the dynamic response of endothelial cells to irradiation. AVAILABILITY AND IMPLEMENTATION: R package 'nsgp' is available at www.ibisc.fr/en/logiciels_arobas.
MOTIVATION: Identifying the set of genes differentially expressed along time is an important task in two-sample time course experiments. Furthermore, estimating at which time periods the differential expression is present can provide additional insight into temporal gene functions. The current differential detection methods are designed to detect difference along observation time intervals or on single measurement points, warranting dense measurements along time to characterize the full temporal differential expression patterns. RESULTS: We propose a novel Bayesian likelihood ratio test to estimate the differential expression time periods. Applying the ratio test to systems of genes provides the temporal response timings and durations of gene expression to a biological condition. We introduce a novel non-stationary Gaussian process as the underlying expression model, with major improvements on model fitness on perturbation and stress experiments. The method is robust to uneven or sparse measurements along time. We assess the performance of the method on realistically simulated dataset and compare against state-of-the-art methods. We additionally apply the method to the analysis of primary human endothelial cells under an ionizing radiation stress to study the transcriptional perturbations over 283 measured genes in an attempt to better understand the role of endothelium in both normal and cancer tissues during radiotherapy. As a result, using the cascade of differential expression periods, domain literature and gene enrichment analysis, we gain insights into the dynamic response of endothelial cells to irradiation. AVAILABILITY AND IMPLEMENTATION: R package 'nsgp' is available at www.ibisc.fr/en/logiciels_arobas.
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