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Automated multi-subject fiber clustering of mouse brain using dominant sets

Mapping of structural and functional connectivity may provide deeper understanding of brain function and disfunction. Diffusion Magnetic Resonance Imaging (DMRI) is a powerful technique to non-invasively delineate white matter (WM) tracts and to obtain a three-dimensional description of the structur...

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Autores principales: Dodero, Luca, Vascon, Sebastiano, Murino, Vittorio, Bifone, Angelo, Gozzi, Alessandro, Sona, Diego
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4290731/
https://www.ncbi.nlm.nih.gov/pubmed/25628561
http://dx.doi.org/10.3389/fninf.2014.00087
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author Dodero, Luca
Vascon, Sebastiano
Murino, Vittorio
Bifone, Angelo
Gozzi, Alessandro
Sona, Diego
author_facet Dodero, Luca
Vascon, Sebastiano
Murino, Vittorio
Bifone, Angelo
Gozzi, Alessandro
Sona, Diego
author_sort Dodero, Luca
collection PubMed
description Mapping of structural and functional connectivity may provide deeper understanding of brain function and disfunction. Diffusion Magnetic Resonance Imaging (DMRI) is a powerful technique to non-invasively delineate white matter (WM) tracts and to obtain a three-dimensional description of the structural architecture of the brain. However, DMRI tractography methods produce highly multi-dimensional datasets whose interpretation requires advanced analytical tools. Indeed, manual identification of specific neuroanatomical tracts based on prior anatomical knowledge is time-consuming and prone to operator-induced bias. Here we propose an automatic multi-subject fiber clustering method that enables retrieval of group-wise WM fiber bundles. In order to account for variance across subjects, we developed a multi-subject approach based on a method known as Dominant Sets algorithm, via an intra- and cross-subject clustering. The intra-subject step allows us to reduce the complexity of the raw tractography data, thus obtaining homogeneous neuroanatomically-plausible bundles in each diffusion space. The cross-subject step, characterized by a proper space-invariant metric in the original diffusion space, enables the identification of the same WM bundles across multiple subjects without any prior neuroanatomical knowledge. Quantitative analysis was conducted comparing our algorithm with spectral clustering and affinity propagation methods on synthetic dataset. We also performed qualitative analysis on mouse brain tractography retrieving significant WM structures. The approach serves the final goal of detecting WM bundles at a population level, thus paving the way to the study of the WM organization across groups.
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spelling pubmed-42907312015-01-27 Automated multi-subject fiber clustering of mouse brain using dominant sets Dodero, Luca Vascon, Sebastiano Murino, Vittorio Bifone, Angelo Gozzi, Alessandro Sona, Diego Front Neuroinform Neuroscience Mapping of structural and functional connectivity may provide deeper understanding of brain function and disfunction. Diffusion Magnetic Resonance Imaging (DMRI) is a powerful technique to non-invasively delineate white matter (WM) tracts and to obtain a three-dimensional description of the structural architecture of the brain. However, DMRI tractography methods produce highly multi-dimensional datasets whose interpretation requires advanced analytical tools. Indeed, manual identification of specific neuroanatomical tracts based on prior anatomical knowledge is time-consuming and prone to operator-induced bias. Here we propose an automatic multi-subject fiber clustering method that enables retrieval of group-wise WM fiber bundles. In order to account for variance across subjects, we developed a multi-subject approach based on a method known as Dominant Sets algorithm, via an intra- and cross-subject clustering. The intra-subject step allows us to reduce the complexity of the raw tractography data, thus obtaining homogeneous neuroanatomically-plausible bundles in each diffusion space. The cross-subject step, characterized by a proper space-invariant metric in the original diffusion space, enables the identification of the same WM bundles across multiple subjects without any prior neuroanatomical knowledge. Quantitative analysis was conducted comparing our algorithm with spectral clustering and affinity propagation methods on synthetic dataset. We also performed qualitative analysis on mouse brain tractography retrieving significant WM structures. The approach serves the final goal of detecting WM bundles at a population level, thus paving the way to the study of the WM organization across groups. Frontiers Media S.A. 2015-01-12 /pmc/articles/PMC4290731/ /pubmed/25628561 http://dx.doi.org/10.3389/fninf.2014.00087 Text en Copyright © 2015 Dodero, Vascon, Murino, Bifone, Gozzi and Sona. 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) or licensor 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
Dodero, Luca
Vascon, Sebastiano
Murino, Vittorio
Bifone, Angelo
Gozzi, Alessandro
Sona, Diego
Automated multi-subject fiber clustering of mouse brain using dominant sets
title Automated multi-subject fiber clustering of mouse brain using dominant sets
title_full Automated multi-subject fiber clustering of mouse brain using dominant sets
title_fullStr Automated multi-subject fiber clustering of mouse brain using dominant sets
title_full_unstemmed Automated multi-subject fiber clustering of mouse brain using dominant sets
title_short Automated multi-subject fiber clustering of mouse brain using dominant sets
title_sort automated multi-subject fiber clustering of mouse brain using dominant sets
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4290731/
https://www.ncbi.nlm.nih.gov/pubmed/25628561
http://dx.doi.org/10.3389/fninf.2014.00087
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