Connectotyping: model based fingerprinting of the functional connectome.
A better characterization of how an individual's brain is functionally organized will likely bring dramatic advances to many fields of study. Here we show a model-based approach toward characterizing resting state functional connectivity MRI (rs-fcMRI) that is capable of identifying a so-called...
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doaj-96b6faf941d0433a9d1e817e78e9e07c2020-11-25T00:08:48ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-01911e11104810.1371/journal.pone.0111048Connectotyping: model based fingerprinting of the functional connectome.Oscar Miranda-DominguezBrian D MillsSamuel D CarpenterKathleen A GrantChristopher D KroenkeJoel T NiggDamien A FairA better characterization of how an individual's brain is functionally organized will likely bring dramatic advances to many fields of study. Here we show a model-based approach toward characterizing resting state functional connectivity MRI (rs-fcMRI) that is capable of identifying a so-called "connectotype", or functional fingerprint in individual participants. The approach rests on a simple linear model that proposes the activity of a given brain region can be described by the weighted sum of its functional neighboring regions. The resulting coefficients correspond to a personalized model-based connectivity matrix that is capable of predicting the timeseries of each subject. Importantly, the model itself is subject specific and has the ability to predict an individual at a later date using a limited number of non-sequential frames. While we show that there is a significant amount of shared variance between models across subjects, the model's ability to discriminate an individual is driven by unique connections in higher order control regions in frontal and parietal cortices. Furthermore, we show that the connectotype is present in non-human primates as well, highlighting the translational potential of the approach.http://europepmc.org/articles/PMC4227655?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Oscar Miranda-Dominguez Brian D Mills Samuel D Carpenter Kathleen A Grant Christopher D Kroenke Joel T Nigg Damien A Fair |
spellingShingle |
Oscar Miranda-Dominguez Brian D Mills Samuel D Carpenter Kathleen A Grant Christopher D Kroenke Joel T Nigg Damien A Fair Connectotyping: model based fingerprinting of the functional connectome. PLoS ONE |
author_facet |
Oscar Miranda-Dominguez Brian D Mills Samuel D Carpenter Kathleen A Grant Christopher D Kroenke Joel T Nigg Damien A Fair |
author_sort |
Oscar Miranda-Dominguez |
title |
Connectotyping: model based fingerprinting of the functional connectome. |
title_short |
Connectotyping: model based fingerprinting of the functional connectome. |
title_full |
Connectotyping: model based fingerprinting of the functional connectome. |
title_fullStr |
Connectotyping: model based fingerprinting of the functional connectome. |
title_full_unstemmed |
Connectotyping: model based fingerprinting of the functional connectome. |
title_sort |
connectotyping: model based fingerprinting of the functional connectome. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2014-01-01 |
description |
A better characterization of how an individual's brain is functionally organized will likely bring dramatic advances to many fields of study. Here we show a model-based approach toward characterizing resting state functional connectivity MRI (rs-fcMRI) that is capable of identifying a so-called "connectotype", or functional fingerprint in individual participants. The approach rests on a simple linear model that proposes the activity of a given brain region can be described by the weighted sum of its functional neighboring regions. The resulting coefficients correspond to a personalized model-based connectivity matrix that is capable of predicting the timeseries of each subject. Importantly, the model itself is subject specific and has the ability to predict an individual at a later date using a limited number of non-sequential frames. While we show that there is a significant amount of shared variance between models across subjects, the model's ability to discriminate an individual is driven by unique connections in higher order control regions in frontal and parietal cortices. Furthermore, we show that the connectotype is present in non-human primates as well, highlighting the translational potential of the approach. |
url |
http://europepmc.org/articles/PMC4227655?pdf=render |
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