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Robust and Fast Markov Chain Monte Carlo Sampling of Diffusion MRI Microstructure Models

In diffusion MRI analysis, advances in biophysical multi-compartment modeling have gained popularity over the conventional Diffusion Tensor Imaging (DTI), because they can obtain a greater specificity in relating the dMRI signal to underlying cellular microstructure. Biophysical multi-compartment mo...

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Autores principales: Harms, Robbert L., Roebroeck, Alard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305549/
https://www.ncbi.nlm.nih.gov/pubmed/30618702
http://dx.doi.org/10.3389/fninf.2018.00097
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author Harms, Robbert L.
Roebroeck, Alard
author_facet Harms, Robbert L.
Roebroeck, Alard
author_sort Harms, Robbert L.
collection PubMed
description In diffusion MRI analysis, advances in biophysical multi-compartment modeling have gained popularity over the conventional Diffusion Tensor Imaging (DTI), because they can obtain a greater specificity in relating the dMRI signal to underlying cellular microstructure. Biophysical multi-compartment models require a parameter estimation, typically performed using either the Maximum Likelihood Estimation (MLE) or the Markov Chain Monte Carlo (MCMC) sampling. Whereas, the MLE provides only a point estimate of the fitted model parameters, the MCMC recovers the entire posterior distribution of the model parameters given in the data, providing additional information such as parameter uncertainty and correlations. MCMC sampling is currently not routinely applied in dMRI microstructure modeling, as it requires adjustment and tuning, specific to each model, particularly in the choice of proposal distributions, burn-in length, thinning, and the number of samples to store. In addition, sampling often takes at least an order of magnitude, more time than non-linear optimization. Here we investigate the performance of the MCMC algorithm variations over multiple popular diffusion microstructure models, to examine whether a single, well performing variation could be applied efficiently and robustly to many models. Using an efficient GPU-based implementation, we showed that run times can be removed as a prohibitive constraint for the sampling of diffusion multi-compartment models. Using this implementation, we investigated the effectiveness of different adaptive MCMC algorithms, burn-in, initialization, and thinning. Finally we applied the theory of the Effective Sample Size, to the diffusion multi-compartment models, as a way of determining a relatively general target for the number of samples needed to characterize parameter distributions for different models and data sets. We conclude that adaptive Metropolis methods increase MCMC performance and select the Adaptive Metropolis-Within-Gibbs (AMWG) algorithm as the primary method. We furthermore advise to initialize the sampling with an MLE point estimate, in which case 100 to 200 samples are sufficient as a burn-in. Finally, we advise against thinning in most use-cases and as a relatively general target for the number of samples, we recommend a multivariate Effective Sample Size of 2,200.
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spelling pubmed-63055492019-01-07 Robust and Fast Markov Chain Monte Carlo Sampling of Diffusion MRI Microstructure Models Harms, Robbert L. Roebroeck, Alard Front Neuroinform Neuroscience In diffusion MRI analysis, advances in biophysical multi-compartment modeling have gained popularity over the conventional Diffusion Tensor Imaging (DTI), because they can obtain a greater specificity in relating the dMRI signal to underlying cellular microstructure. Biophysical multi-compartment models require a parameter estimation, typically performed using either the Maximum Likelihood Estimation (MLE) or the Markov Chain Monte Carlo (MCMC) sampling. Whereas, the MLE provides only a point estimate of the fitted model parameters, the MCMC recovers the entire posterior distribution of the model parameters given in the data, providing additional information such as parameter uncertainty and correlations. MCMC sampling is currently not routinely applied in dMRI microstructure modeling, as it requires adjustment and tuning, specific to each model, particularly in the choice of proposal distributions, burn-in length, thinning, and the number of samples to store. In addition, sampling often takes at least an order of magnitude, more time than non-linear optimization. Here we investigate the performance of the MCMC algorithm variations over multiple popular diffusion microstructure models, to examine whether a single, well performing variation could be applied efficiently and robustly to many models. Using an efficient GPU-based implementation, we showed that run times can be removed as a prohibitive constraint for the sampling of diffusion multi-compartment models. Using this implementation, we investigated the effectiveness of different adaptive MCMC algorithms, burn-in, initialization, and thinning. Finally we applied the theory of the Effective Sample Size, to the diffusion multi-compartment models, as a way of determining a relatively general target for the number of samples needed to characterize parameter distributions for different models and data sets. We conclude that adaptive Metropolis methods increase MCMC performance and select the Adaptive Metropolis-Within-Gibbs (AMWG) algorithm as the primary method. We furthermore advise to initialize the sampling with an MLE point estimate, in which case 100 to 200 samples are sufficient as a burn-in. Finally, we advise against thinning in most use-cases and as a relatively general target for the number of samples, we recommend a multivariate Effective Sample Size of 2,200. Frontiers Media S.A. 2018-12-18 /pmc/articles/PMC6305549/ /pubmed/30618702 http://dx.doi.org/10.3389/fninf.2018.00097 Text en Copyright © 2018 Harms and Roebroeck. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Harms, Robbert L.
Roebroeck, Alard
Robust and Fast Markov Chain Monte Carlo Sampling of Diffusion MRI Microstructure Models
title Robust and Fast Markov Chain Monte Carlo Sampling of Diffusion MRI Microstructure Models
title_full Robust and Fast Markov Chain Monte Carlo Sampling of Diffusion MRI Microstructure Models
title_fullStr Robust and Fast Markov Chain Monte Carlo Sampling of Diffusion MRI Microstructure Models
title_full_unstemmed Robust and Fast Markov Chain Monte Carlo Sampling of Diffusion MRI Microstructure Models
title_short Robust and Fast Markov Chain Monte Carlo Sampling of Diffusion MRI Microstructure Models
title_sort robust and fast markov chain monte carlo sampling of diffusion mri microstructure models
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305549/
https://www.ncbi.nlm.nih.gov/pubmed/30618702
http://dx.doi.org/10.3389/fninf.2018.00097
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