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      FunMaps: a method for parcellating functional brain networks using resting-state functional MRI data

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          Abstract

          Parcellations of resting-state functional magnetic resonance imaging (rs-fMRI) data are widely used to create topographical maps of functional networks in the human brain. While such network maps are highly useful for studying brain organization and function, they usually require large sample sizes to make them, thus creating practical limitations for researchers that would like to carry out parcellations on data collected in their labs. Furthermore, it can be difficult to quantitatively evaluate the results of a parcellation since networks are usually identified using a clustering algorithm, like principal components analysis, on the results of a single group-averaged connectivity map. To address these challenges, we developed the FunMaps method: a parcellation routine that intrinsically incorporates stability and replicability of the parcellation by keeping only network distinctions that agree across halves of the data over multiple random iterations. Here, we demonstrate the efficacy and flexibility of FunMaps, while describing step-by-step instructions for running the program. The FunMaps method is publicly available on GitHub ( https://github.com/persichetti-lab/FunMaps). It includes source code for running the parcellation and auxiliary code for preparing data, evaluating the parcellation, and displaying the results.

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          Most cited references35

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          The organization of the human cerebral cortex estimated by intrinsic functional connectivity.

          Information processing in the cerebral cortex involves interactions among distributed areas. Anatomical connectivity suggests that certain areas form local hierarchical relations such as within the visual system. Other connectivity patterns, particularly among association areas, suggest the presence of large-scale circuits without clear hierarchical relations. In this study the organization of networks in the human cerebrum was explored using resting-state functional connectivity MRI. Data from 1,000 subjects were registered using surface-based alignment. A clustering approach was employed to identify and replicate networks of functionally coupled regions across the cerebral cortex. The results revealed local networks confined to sensory and motor cortices as well as distributed networks of association regions. Within the sensory and motor cortices, functional connectivity followed topographic representations across adjacent areas. In association cortex, the connectivity patterns often showed abrupt transitions between network boundaries. Focused analyses were performed to better understand properties of network connectivity. A canonical sensory-motor pathway involving primary visual area, putative middle temporal area complex (MT+), lateral intraparietal area, and frontal eye field was analyzed to explore how interactions might arise within and between networks. Results showed that adjacent regions of the MT+ complex demonstrate differential connectivity consistent with a hierarchical pathway that spans networks. The functional connectivity of parietal and prefrontal association cortices was next explored. Distinct connectivity profiles of neighboring regions suggest they participate in distributed networks that, while showing evidence for interactions, are embedded within largely parallel, interdigitated circuits. We conclude by discussing the organization of these large-scale cerebral networks in relation to monkey anatomy and their potential evolutionary expansion in humans to support cognition.
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            A multi-modal parcellation of human cerebral cortex

            Understanding the amazingly complex human cerebral cortex requires a map (or parcellation) of its major subdivisions, known as cortical areas. Making an accurate areal map has been a century-old objective in neuroscience. Using multi-modal magnetic resonance images from the Human Connectome Project (HCP) and an objective semi-automated neuroanatomical approach, we delineated 180 areas per hemisphere bounded by sharp changes in cortical architecture, function, connectivity, and/or topography in a precisely aligned group average of 210 healthy young adults. We characterized 97 new areas and 83 areas previously reported using post-mortem microscopy or other specialized study-specific approaches. To enable automated delineation and identification of these areas in new HCP subjects and in future studies, we trained a machine-learning classifier to recognize the multi-modal ‘fingerprint’ of each cortical area. This classifier detected the presence of 96.6% of the cortical areas in new subjects, replicated the group parcellation, and could correctly locate areas in individuals with atypical parcellations. The freely available parcellation and classifier will enable substantially improved neuroanatomical precision for studies of the structural and functional organization of human cerebral cortex and its variation across individuals and in development, aging, and disease.
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              A component based noise correction method (CompCor) for BOLD and perfusion based fMRI.

              A component based method (CompCor) for the reduction of noise in both blood oxygenation level-dependent (BOLD) and perfusion-based functional magnetic resonance imaging (fMRI) data is presented. In the proposed method, significant principal components are derived from noise regions-of-interest (ROI) in which the time series data are unlikely to be modulated by neural activity. These components are then included as nuisance parameters within general linear models for BOLD and perfusion-based fMRI time series data. Two approaches for the determination of the noise ROI are considered. The first method uses high-resolution anatomical data to define a region of interest composed primarily of white matter and cerebrospinal fluid, while the second method defines a region based upon the temporal standard deviation of the time series data. With the application of CompCor, the temporal standard deviation of resting-state perfusion and BOLD data in gray matter regions was significantly reduced as compared to either no correction or the application of a previously described retrospective image based correction scheme (RETROICOR). For both functional perfusion and BOLD data, the application of CompCor significantly increased the number of activated voxels as compared to no correction. In addition, for functional BOLD data, there were significantly more activated voxels detected with CompCor as compared to RETROICOR. In comparison to RETROICOR, CompCor has the advantage of not requiring external monitoring of physiological fluctuations.
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                Author and article information

                Contributors
                URI : https://loop.frontiersin.org/people/2431302/overviewRole: Role: Role: Role: Role: Role: Role: Role: Role:
                URI : https://loop.frontiersin.org/people/8770/overviewRole: Role: Role: Role: Role: Role: Role: Role:
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                URI : https://loop.frontiersin.org/people/8773/overviewRole: Role: Role: Role: Role: Role:
                URI : https://loop.frontiersin.org/people/2396704/overviewRole: Role: Role: Role: Role: Role: Role: Role: Role: Role: Role: Role: Role:
                Journal
                Front Hum Neurosci
                Front Hum Neurosci
                Front. Hum. Neurosci.
                Frontiers in Human Neuroscience
                Frontiers Media S.A.
                1662-5161
                24 September 2024
                2024
                : 18
                : 1461590
                Affiliations
                Section on Cognitive Neuropsychology, Laboratory of Brain and Cognition, National Institute of Mental Health, National Institutes of Health , Bethesda, MD, United States
                Author notes

                Edited by: Seiki Konishi, Juntendo University, Japan

                Reviewed by: Marc N. Coutanche, University of Pittsburgh, United States

                Teppei Matsui, Doshisha University Graduate School of Brain Science, Japan

                Gia H. Ngo, Cornell University, United States

                *Correspondence: Andrew S. Persichetti, persichettias@ 123456nih.gov
                Article
                10.3389/fnhum.2024.1461590
                11458417
                39381142
                acc272ca-f34e-4e61-bf50-877d2ecf42f8
                Copyright © 2024 Shao, Gotts, Li, Martin and Persichetti.

                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.

                History
                : 08 July 2024
                : 11 September 2024
                Page count
                Figures: 6, Tables: 1, Equations: 0, References: 36, Pages: 12, Words: 8622
                Funding
                Funded by: NIMH Intramural Research Program
                Award ID: (#ZIA MH002920-09
                Funded by: National Institute of Mental Health of the National Institutes of Health
                Award ID: U01MH109589
                The author(s) declare that financial support was received for the research, authorship, and/or publication of this article. Research reported in this publication was supported by the NIMH Intramural Research Program (#ZIA MH002920-09, clinical trials number NCT01031407), the National Institute of Mental Health of the National Institutes of Health under Award Number U01MH109589 and by funds provided by the McDonnell Center for Systems Neuroscience at Washington University in St. Louis. The HCP-Development 2.0 Release data used in this report came from DOI: 10.15154/1520708.
                Categories
                Human Neuroscience
                Methods
                Custom metadata
                Cognitive Neuroscience

                Neurosciences
                resting-state,fmri,functional connectivity,parcellation,brain networks
                Neurosciences
                resting-state, fmri, functional connectivity, parcellation, brain networks

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