Abstract

We have proposed a Bayesian approach for functional parcellation of whole-brain FMRI measurements which we call Clustered Activity Estimation with Spatial Adjacency Restrictions (CAESAR). We use distance-dependent Chinese restaurant processes (dd-CRPs) to define a flexible prior which partitions the voxel measurements into clusters whose number and shapes are unknown a priori. With dd-CRPs we can conveniently implement spatial constraints to ensure that our parcellations remain spatially contiguous and thereby physiologically meaningful. In the present work, we extend CAESAR by using Gaussian process (GP) priors to model the temporally smooth haemodynamic signals that give rise to the measured FMRI data. A challenge for GP inference in our setting is the cubic scaling with respect to the number of time points, which can become computationally prohibitive with FMRI measurements, potentially consisting of long time series. As a solution we describe an efficient implementation that is practically as fast as the corresponding time-independent non-GP model with typically-sized FMRI data sets. We also employ a population Monte-Carlo algorithm that can significantly speed up convergence compared to traditional single-chain methods. First we illustrate the benefits of CAESAR and the GP priors with simulated experiments. Next, we demonstrate our approach by parcellating resting state FMRI data measured from twenty participants as taken from the Human Connectome Project data repository. Results show that CAESAR affords highly robust and scalable whole-brain clustering of FMRI timecourses.

Highlights

  • The brain is generally assumed to consist of interconnected functional modules

  • We addressed the computational challenges that emerge from this extension and show that the resulting approach allows efficient and robust estimation of whole-brain parcellations from functional magnetic resonance imaging (FMRI) timecourses

  • We will first describe Clustered Activity Estimation with Spatial Adjacency Restrictions (CAESAR) performance on simulated data, followed by results obtained with rsFMRI data

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Summary

Introduction

The brain is generally assumed to consist of interconnected functional modules. This principle takes central stage in connectomics research, referring to the study of the properties of these connection patterns [1]. Connectomics presupposes some definition of nodes to be connected. This node definition can be linked to different scales, ranging from single neurons to brain regions. The scale of node definition is dictated by the measurement.

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