Dynamic Bayesian Network for Reliability of Mechatronic System with Taking Account the Multi-Domain Interaction

This article presents a methodology for reliability prediction during the design phase of mechatronic system considered as an interactive dynamic system. The difficulty in modeling reliability of a mechatronic system is mainly due to failures related to the interaction between the different domains called Multi-domain interaction. Therefore in this paper, after a presentation of the state of the art of mechatronic systems reliability estimation methods, we propose a original approach by representing multi domain interactions by influential factors in the dysfunctional modeled by Dynamic Bayesian Networks. A case study demonstrates the interest of the proposed approach

Identifying interactions in the time and frequency domains in local and global networks : a Granger causality approach

Background Reverse-engineering approaches such as Bayesian network inference, ordinary differential equations (ODEs) and information theory are widely applied to deriving causal relationships among different elements such as genes, proteins, metabolites, neurons, brain areas and so on, based upon multi-dimensional spatial and temporal data. There are several well-established reverse-engineering approaches to explore causal relationships in a dynamic network, such as ordinary differential equations (ODE), Bayesian networks, information theory and Granger Causality. Results Here we focused on Granger causality both in the time and frequency domain and in local and global networks, and applied our approach to experimental data (genes and proteins). For a small gene network, Granger causality outperformed all the other three approaches mentioned above. A global protein network of 812 proteins was reconstructed, using a novel approach. The obtained results fitted well with known experimental findings and predicted many experimentally testable results. In addition to interactions in the time domain, interactions in the frequency domain were also recovered. Conclusions The results on the proteomic data and gene data confirm that Granger causality is a simple and accurate approach to recover the network structure. Our approach is general and can be easily applied to other types of temporal data

Novel Bayesian Networks for Genomic Prediction of Developmental Traits in Biomass Sorghum.

The ability to connect genetic information between traits over time allow Bayesian networks to offer a powerful probabilistic framework to construct genomic prediction models. In this study, we phenotyped a diversity panel of 869 biomass sorghum (Sorghum bicolor (L.) Moench) lines, which had been genotyped with 100,435 SNP markers, for plant height (PH) with biweekly measurements from 30 to 120 days after planting (DAP) and for end-of-season dry biomass yield (DBY) in four environments. We evaluated five genomic prediction models: Bayesian network (BN), Pleiotropic Bayesian network (PBN), Dynamic Bayesian network (DBN), multi-trait GBLUP (MTr-GBLUP), and multi-time GBLUP (MTi-GBLUP) models. In fivefold cross-validation, prediction accuracies ranged from 0.46 (PBN) to 0.49 (MTr-GBLUP) for DBY and from 0.47 (DBN, DAP120) to 0.75 (MTi-GBLUP, DAP60) for PH. Forward-chaining cross-validation further improved prediction accuracies of the DBN, MTi-GBLUP and MTr-GBLUP models for PH (training slice: 30-45 DAP) by 36.4-52.4% relative to the BN and PBN models. Coincidence indices (target: biomass, secondary: PH) and a coincidence index based on lines (PH time series) showed that the ranking of lines by PH changed minimally after 45 DAP. These results suggest a two-level indirect selection method for PH at harvest (first-level target trait) and DBY (second-level target trait) could be conducted earlier in the season based on ranking of lines by PH at 45 DAP (secondary trait). With the advance of high-throughput phenotyping technologies, our proposed two-level indirect selection framework could be valuable for enhancing genetic gain per unit of time when selecting on developmental traits

Dynamic Bayesian networks for integrating multi-omics time-series microbiome data

. A key challenge in the analysis of longitudinal microbiomes data is to go beyond computing their compositional profiles and infer the complex web of interactions between the various microbial taxa, their genes, and the metabolites they consume and produce. To address this challenge, we developed a computational pipeline that first aligns multi-omics data and then uses dynamic Bayesian networks (DBNs) to integrate them into a unified model. We discuss how our approach handles the different sampling and progression rates between individuals, how we reduce the large number of different entities and parameters in the DBNs, and the construction and use of a validation set to model edges. Applying our method to data collected from Inflammatory Bowel Disease (IBD) patients, we show that it can accurately identify known and novel interactions between various entities and can improve on current methods for learning such interactions. Experimental validations support several predictions about novel metabolite-taxa interactions. The source code is freely available under the MIT Open Source license agreement and can be downloaded from https://github.com/DaniRuizPerez/longitudinal_multiomic_analysis_public

Dynamic bayesian networks for integrating multi-omics time series microbiome data

A key challenge in the analysis of longitudinal microbiome data is theinference of temporal interactions between microbial taxa, their genes, the metabolites that they consume and produce, and host genes. To address these challenges,we developed a computational pipeline, a pipeline for the analysis of longitudinalmulti-omics data (PALM), that first aligns multi-omics data and then uses dynamicBayesian networks (DBNs) to reconstruct a unified model. Our approach overcomesdifferences in sampling and progression rates, utilizes a biologically inspired multiomic framework, reduces the large number of entities and parameters in the DBNs,and validates the learned network. Applying PALM to data collected from inflammatory bowel disease patients, we show that it accurately identifies known and novelinteractions. Targeted experimental validations further support a number of the predicted novel metabolite-taxon interactionsFil: Ruiz Perez, Daniel. Florida International University; Estados UnidosFil: Lugo Martinez, Jose. University of Carnegie Mellon; Estados UnidosFil: Bourguignon, Natalia. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Florida International University; Estados Unidos. Universidad Tecnológica Nacional; ArgentinaFil: Mathee, Kalai. Florida International University; Estados UnidosFil: Lerner, Betiana. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Tecnológica Nacional; ArgentinaFil: Bar Joseph, Ziv. University of Carnegie Mellon; Estados UnidosFil: Narasimhan, Giri. Florida International University; Estados Unido