Mpdcm: A toolbox for massively parallel dynamic causal modeling

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Abstract

Background: Dynamic causal modeling (DCM) for fMRI is an established method for Bayesian system identification and inference on effective brain connectivity. DCM relies on a biophysical model that links hidden neuronal activity to measurable BOLD signals. Currently, biophysical simulations from DCM constitute a serious computational hindrance. Here, we present Massively Parallel Dynamic Causal Modeling (. mpdcm), a toolbox designed to address this bottleneck. New method: mpdcm delegates the generation of simulations from DCM's biophysical model to graphical processing units (GPUs). Simulations are generated in parallel by implementing a low storage explicit Runge-Kutta's scheme on a GPU architecture. mpdcm is publicly available under the GPLv3 license. Results: We found that mpdcm efficiently generates large number of simulations without compromising their accuracy. As applications of mpdcm, we suggest two computationally expensive sampling algorithms: thermodynamic integration and parallel tempering. Comparison with existing method(s): mpdcm is up to two orders of magnitude more efficient than the standard implementation in the software package SPM. Parallel tempering increases the mixing properties of the traditional Metropolis-Hastings algorithm at low computational cost given efficient, parallel simulations of a model. Conclusions: Future applications of DCM will likely require increasingly large computational resources, for example, when the likelihood landscape of a model is multimodal, or when implementing sampling methods for multi-subject analysis. Due to the wide availability of GPUs, algorithmic advances can be readily available in the absence of access to large computer grids, or when there is a lack of expertise to implement algorithms in such grids.

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APA

Aponte, E. A., Raman, S., Sengupta, B., Penny, W. D., Stephan, K. E., & Heinzle, J. (2016). Mpdcm: A toolbox for massively parallel dynamic causal modeling. Journal of Neuroscience Methods, 257, 7–16. https://doi.org/10.1016/j.jneumeth.2015.09.009

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