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Isolating the sources of pipeline‐variability in group‐level task‐fMRI results

Task‐fMRI researchers have great flexibility as to how they analyze their data, with multiple methodological options to choose from at each stage of the analysis workflow. While the development of tools and techniques has broadened our horizons for comprehending the complexities of the human brain,...

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Autores principales: Bowring, Alexander, Nichols, Thomas E., Maumet, Camille
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8764489/
https://www.ncbi.nlm.nih.gov/pubmed/34773436
http://dx.doi.org/10.1002/hbm.25713
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author Bowring, Alexander
Nichols, Thomas E.
Maumet, Camille
author_facet Bowring, Alexander
Nichols, Thomas E.
Maumet, Camille
author_sort Bowring, Alexander
collection PubMed
description Task‐fMRI researchers have great flexibility as to how they analyze their data, with multiple methodological options to choose from at each stage of the analysis workflow. While the development of tools and techniques has broadened our horizons for comprehending the complexities of the human brain, a growing body of research has highlighted the pitfalls of such methodological plurality. In a recent study, we found that the choice of software package used to run the analysis pipeline can have a considerable impact on the final group‐level results of a task‐fMRI investigation (Bowring et al., 2019, BMN). Here we revisit our work, seeking to identify the stages of the pipeline where the greatest variation between analysis software is induced. We carry out further analyses on the three datasets evaluated in BMN, employing a common processing strategy across parts of the analysis workflow and then utilizing procedures from three software packages (AFNI, FSL, and SPM) across the remaining steps of the pipeline. We use quantitative methods to compare the statistical maps and isolate the main stages of the workflow where the three packages diverge. Across all datasets, we find that variation between the packages' results is largely attributable to a handful of individual analysis stages, and that these sources of variability were heterogeneous across the datasets (e.g., choice of first‐level signal model had the most impact for the balloon analog risk task dataset, while first‐level noise model and group‐level model were more influential for the false belief and antisaccade task datasets, respectively). We also observe areas of the analysis workflow where changing the software package causes minimal differences in the final results, finding that the group‐level results were largely unaffected by which software package was used to model the low‐frequency fMRI drifts.
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spelling pubmed-87644892022-01-21 Isolating the sources of pipeline‐variability in group‐level task‐fMRI results Bowring, Alexander Nichols, Thomas E. Maumet, Camille Hum Brain Mapp Research Articles Task‐fMRI researchers have great flexibility as to how they analyze their data, with multiple methodological options to choose from at each stage of the analysis workflow. While the development of tools and techniques has broadened our horizons for comprehending the complexities of the human brain, a growing body of research has highlighted the pitfalls of such methodological plurality. In a recent study, we found that the choice of software package used to run the analysis pipeline can have a considerable impact on the final group‐level results of a task‐fMRI investigation (Bowring et al., 2019, BMN). Here we revisit our work, seeking to identify the stages of the pipeline where the greatest variation between analysis software is induced. We carry out further analyses on the three datasets evaluated in BMN, employing a common processing strategy across parts of the analysis workflow and then utilizing procedures from three software packages (AFNI, FSL, and SPM) across the remaining steps of the pipeline. We use quantitative methods to compare the statistical maps and isolate the main stages of the workflow where the three packages diverge. Across all datasets, we find that variation between the packages' results is largely attributable to a handful of individual analysis stages, and that these sources of variability were heterogeneous across the datasets (e.g., choice of first‐level signal model had the most impact for the balloon analog risk task dataset, while first‐level noise model and group‐level model were more influential for the false belief and antisaccade task datasets, respectively). We also observe areas of the analysis workflow where changing the software package causes minimal differences in the final results, finding that the group‐level results were largely unaffected by which software package was used to model the low‐frequency fMRI drifts. John Wiley & Sons, Inc. 2021-11-13 /pmc/articles/PMC8764489/ /pubmed/34773436 http://dx.doi.org/10.1002/hbm.25713 Text en © 2021 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Bowring, Alexander
Nichols, Thomas E.
Maumet, Camille
Isolating the sources of pipeline‐variability in group‐level task‐fMRI results
title Isolating the sources of pipeline‐variability in group‐level task‐fMRI results
title_full Isolating the sources of pipeline‐variability in group‐level task‐fMRI results
title_fullStr Isolating the sources of pipeline‐variability in group‐level task‐fMRI results
title_full_unstemmed Isolating the sources of pipeline‐variability in group‐level task‐fMRI results
title_short Isolating the sources of pipeline‐variability in group‐level task‐fMRI results
title_sort isolating the sources of pipeline‐variability in group‐level task‐fmri results
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8764489/
https://www.ncbi.nlm.nih.gov/pubmed/34773436
http://dx.doi.org/10.1002/hbm.25713
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