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Local-Global Parcellation of the Human Cerebral Cortex From Intrinsic Functional Connectivity MRI

Alexander Schaefer, Ru Kong, Evan M. Gordon, Timothy O. Laumann, View ORCID ProfileXi-Nian Zuo, View ORCID ProfileAvram J. Holmes, View ORCID ProfileSimon B. Eickhoff, View ORCID ProfileB. T. Thomas Yeo
doi: https://doi.org/10.1101/135632
Alexander Schaefer
1ASTAR-NUS Clinical Imaging Research Centre, Department of Electrical and Computer Engineering, Singapore Institute for Neurotechnology and Memory Networks Program, National University of Singapore, Singapore
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Ru Kong
1ASTAR-NUS Clinical Imaging Research Centre, Department of Electrical and Computer Engineering, Singapore Institute for Neurotechnology and Memory Networks Program, National University of Singapore, Singapore
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Evan M. Gordon
2VISN 17 Center of Excellence for Research on Returning War Veterans, Waco, TX, USA
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Timothy O. Laumann
3Washington University in St. Louis, St. Louis, MO, USA
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Xi-Nian Zuo
4CAS Key Laboratory of Behavioral Sciences, Institute of Psychology, Beijing, China
5University of Chinese Academy of Sciences, Beijing, China
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Avram J. Holmes
6Yale University, New Haven, CT, USA
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Simon B. Eickhoff
7Institute for Systems Neuroscience, Medical Faculty, Heinrich-Heine University, Düsseldorf, Germany
8Institute of Neuroscience and Medicine (INM-1, INM-7), Research Center Jülich, Jülich, Germany
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B. T. Thomas Yeo
1ASTAR-NUS Clinical Imaging Research Centre, Department of Electrical and Computer Engineering, Singapore Institute for Neurotechnology and Memory Networks Program, National University of Singapore, Singapore
9Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Charlestown, MA, USA
10Centre for Cognitive Neuroscience, Duke-NUS Medical School, Singapore
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Abstract

A central goal in systems neuroscience is the parcellation of the cerebral cortex into discrete neurobiological “atoms”. Resting-state functional magnetic resonance imaging (rs-fMRI) offers the possibility of in-vivo human cortical parcellation. Almost all previous parcellations relied on one of two approaches. The local gradient approach detects abrupt transitions in functional connectivity patterns. These transitions potentially reflect cortical areal boundaries defined by histology or visuotopic fMRI. By contrast, the global similarity approach clusters similar functional connectivity patterns regardless of spatial proximity, resulting in parcels with homogeneous (similar) rs-fMRI signals. Here we propose a gradient-weighted Markov Random Field (gwMRF) model integrating local gradient and global similarity approaches. Using task-fMRI and rs-fMRI across diverse acquisition protocols, we found gwMRF parcellations to be more homogeneous than four previously published parcellations. Furthermore, gwMRF parcellations agreed with the boundaries of certain cortical areas defined using histology and visuotopic fMRI. Some parcels captured sub-areal (somatotopic and visuotopic) features that likely reflect distinct computational units within known cortical areas. These results suggest that gwMRF parcellations reveal neurobiologically meaningful features of brain organization and are potentially useful for future applications requiring dimensionality reduction of voxel-wise fMRI data. Multi-resolution parcellations generated from 1489 participants are available (https://github.com/ThomasYeoLab/CBIG/tree/master/stable_projects/brain_parcellation/Schaefer2018_LocalGlobal)

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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted July 16, 2017.
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Local-Global Parcellation of the Human Cerebral Cortex From Intrinsic Functional Connectivity MRI
Alexander Schaefer, Ru Kong, Evan M. Gordon, Timothy O. Laumann, Xi-Nian Zuo, Avram J. Holmes, Simon B. Eickhoff, B. T. Thomas Yeo
bioRxiv 135632; doi: https://doi.org/10.1101/135632
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Local-Global Parcellation of the Human Cerebral Cortex From Intrinsic Functional Connectivity MRI
Alexander Schaefer, Ru Kong, Evan M. Gordon, Timothy O. Laumann, Xi-Nian Zuo, Avram J. Holmes, Simon B. Eickhoff, B. T. Thomas Yeo
bioRxiv 135632; doi: https://doi.org/10.1101/135632

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