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dc.contributor.authorFerrat, LA
dc.contributor.authorGoodfellow, M
dc.contributor.authorTerry, JR
dc.date.accessioned2018-03-19T08:42:32Z
dc.date.issued2018-03-02
dc.description.abstractNeural mass models (NMMs) are increasingly used to uncover the large-scale mechanisms of brain rhythms in health and disease. The dynamics of these models is dependent upon the choice of parameters, and therefore it is crucial to be able to understand how dynamics change when parameters are varied. Despite being considered low dimensional in comparison to micro-scale, neuronal network models, with regards to understanding the relationship between parameters and dynamics, NMMs are still prohibitively high dimensional for classical approaches such as numerical continuation. Therefore, we need alternative methods to characterise dynamics of NMMs in high dimensional parameter spaces. Here, we introduce a statistical framework that enables the efficient exploration of the relationship between model parameters and selected features of the simulated, emergent model dynamics of NMMs. We combine the classical machine learning approaches of trees and random forests to enable studying the effect that varying multiple parameters has on the dynamics of a model. The method proceeds by using simulations to transform the mathematical model into a database. This database is then used to partition parameter space with respect to dynamic features of interest, using random forests. This allows us to rapidly explore dynamics in high dimensional parameter space, capture the approximate location of qualitative transitions in dynamics and assess the relative importance of all parameters in the model in all dimensions simultaneously. We apply this method to a commonly used NMM in the context of transitions to seizure dynamics. We find that the inhibitory sub-system is most crucial for the generation of seizure dynamics, confirm and expand previous findings regarding the ratio of excitation and inhibition, and demonstrate that previously overlooked parameters can have a significant impact on model dynamics. We advocate the use of this method in future to constrain high dimensional parameter spaces enabling more efficient, person-specific, model calibration.en_GB
dc.description.sponsorshipMG and JRT acknowledge the generous support of a Wellcome Trust Institutional Strategic Support Award (https://wellcome.ac.uk/) via grant WT105618MA. They further acknowledge financial support from Engineering and Physical Sciences Research Council (https://www.epsrc.ac.uk/) via grant EP/N014391/1. JRT acknowledges the financial support of the MRC via grant MR/K013998/1. LAF was generously supported by a PhD studentship from the College of Engineering, Mathematics and Physical Science at the University of Exeter.en_GB
dc.identifier.citationVol. 14, e1006009en_GB
dc.identifier.doi10.1371/journal.pcbi.1006009
dc.identifier.otherPCOMPBIOL-D-17-01653
dc.identifier.urihttp://hdl.handle.net/10871/32148
dc.language.isoenen_GB
dc.publisherPublic Library of Science (PLoS)en_GB
dc.relation.sourceAll relevant data are within the paper and its Supporting Information files.en_GB
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pubmed/29499044en_GB
dc.rightsCopyright: © 2018 Ferrat et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.en_GB
dc.titleClassifying dynamic transitions in high dimensional neural mass models: A random forest approach.en_GB
dc.typeArticleen_GB
dc.date.available2018-03-19T08:42:32Z
dc.identifier.issn1553-734X
exeter.place-of-publicationUnited Statesen_GB
dc.descriptionThis is the author accepted manuscript. The final version is available from the publisher via the DOI in this record.en_GB
dc.identifier.journalPLoS Computational Biologyen_GB


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