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GLMdenoise: a fast, automated technique for denoising task-based fMRI data

In task-based functional magnetic resonance imaging (fMRI), researchers seek to measure fMRI signals related to a given task or condition. In many circumstances, measuring this signal of interest is limited by noise. In this study, we present GLMdenoise, a technique that improves signal-to-noise rat...

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Autores principales: Kay, Kendrick N., Rokem, Ariel, Winawer, Jonathan, Dougherty, Robert F., Wandell, Brian A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3865440/
https://www.ncbi.nlm.nih.gov/pubmed/24381539
http://dx.doi.org/10.3389/fnins.2013.00247
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author Kay, Kendrick N.
Rokem, Ariel
Winawer, Jonathan
Dougherty, Robert F.
Wandell, Brian A.
author_facet Kay, Kendrick N.
Rokem, Ariel
Winawer, Jonathan
Dougherty, Robert F.
Wandell, Brian A.
author_sort Kay, Kendrick N.
collection PubMed
description In task-based functional magnetic resonance imaging (fMRI), researchers seek to measure fMRI signals related to a given task or condition. In many circumstances, measuring this signal of interest is limited by noise. In this study, we present GLMdenoise, a technique that improves signal-to-noise ratio (SNR) by entering noise regressors into a general linear model (GLM) analysis of fMRI data. The noise regressors are derived by conducting an initial model fit to determine voxels unrelated to the experimental paradigm, performing principal components analysis (PCA) on the time-series of these voxels, and using cross-validation to select the optimal number of principal components to use as noise regressors. Due to the use of data resampling, GLMdenoise requires and is best suited for datasets involving multiple runs (where conditions repeat across runs). We show that GLMdenoise consistently improves cross-validation accuracy of GLM estimates on a variety of event-related experimental datasets and is accompanied by substantial gains in SNR. To promote practical application of methods, we provide MATLAB code implementing GLMdenoise. Furthermore, to help compare GLMdenoise to other denoising methods, we present the Denoise Benchmark (DNB), a public database and architecture for evaluating denoising methods. The DNB consists of the datasets described in this paper, a code framework that enables automatic evaluation of a denoising method, and implementations of several denoising methods, including GLMdenoise, the use of motion parameters as noise regressors, ICA-based denoising, and RETROICOR/RVHRCOR. Using the DNB, we find that GLMdenoise performs best out of all of the denoising methods we tested.
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spelling pubmed-38654402013-12-31 GLMdenoise: a fast, automated technique for denoising task-based fMRI data Kay, Kendrick N. Rokem, Ariel Winawer, Jonathan Dougherty, Robert F. Wandell, Brian A. Front Neurosci Neuroscience In task-based functional magnetic resonance imaging (fMRI), researchers seek to measure fMRI signals related to a given task or condition. In many circumstances, measuring this signal of interest is limited by noise. In this study, we present GLMdenoise, a technique that improves signal-to-noise ratio (SNR) by entering noise regressors into a general linear model (GLM) analysis of fMRI data. The noise regressors are derived by conducting an initial model fit to determine voxels unrelated to the experimental paradigm, performing principal components analysis (PCA) on the time-series of these voxels, and using cross-validation to select the optimal number of principal components to use as noise regressors. Due to the use of data resampling, GLMdenoise requires and is best suited for datasets involving multiple runs (where conditions repeat across runs). We show that GLMdenoise consistently improves cross-validation accuracy of GLM estimates on a variety of event-related experimental datasets and is accompanied by substantial gains in SNR. To promote practical application of methods, we provide MATLAB code implementing GLMdenoise. Furthermore, to help compare GLMdenoise to other denoising methods, we present the Denoise Benchmark (DNB), a public database and architecture for evaluating denoising methods. The DNB consists of the datasets described in this paper, a code framework that enables automatic evaluation of a denoising method, and implementations of several denoising methods, including GLMdenoise, the use of motion parameters as noise regressors, ICA-based denoising, and RETROICOR/RVHRCOR. Using the DNB, we find that GLMdenoise performs best out of all of the denoising methods we tested. Frontiers Media S.A. 2013-12-17 /pmc/articles/PMC3865440/ /pubmed/24381539 http://dx.doi.org/10.3389/fnins.2013.00247 Text en Copyright © 2013 Kay, Rokem, Winawer, Dougherty and Wandell. http://creativecommons.org/licenses/by/3.0/ 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
Kay, Kendrick N.
Rokem, Ariel
Winawer, Jonathan
Dougherty, Robert F.
Wandell, Brian A.
GLMdenoise: a fast, automated technique for denoising task-based fMRI data
title GLMdenoise: a fast, automated technique for denoising task-based fMRI data
title_full GLMdenoise: a fast, automated technique for denoising task-based fMRI data
title_fullStr GLMdenoise: a fast, automated technique for denoising task-based fMRI data
title_full_unstemmed GLMdenoise: a fast, automated technique for denoising task-based fMRI data
title_short GLMdenoise: a fast, automated technique for denoising task-based fMRI data
title_sort glmdenoise: a fast, automated technique for denoising task-based fmri data
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3865440/
https://www.ncbi.nlm.nih.gov/pubmed/24381539
http://dx.doi.org/10.3389/fnins.2013.00247
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