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      The relation between statistical power and inference in fMRI

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      1 , * , 2 , 3
      PLoS ONE
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          Abstract

          Statistically underpowered studies can result in experimental failure even when all other experimental considerations have been addressed impeccably. In fMRI the combination of a large number of dependent variables, a relatively small number of observations (subjects), and a need to correct for multiple comparisons can decrease statistical power dramatically. This problem has been clearly addressed yet remains controversial—especially in regards to the expected effect sizes in fMRI, and especially for between-subjects effects such as group comparisons and brain-behavior correlations. We aimed to clarify the power problem by considering and contrasting two simulated scenarios of such possible brain-behavior correlations: weak diffuse effects and strong localized effects. Sampling from these scenarios shows that, particularly in the weak diffuse scenario, common sample sizes (n = 20–30) display extremely low statistical power, poorly represent the actual effects in the full sample, and show large variation on subsequent replications. Empirical data from the Human Connectome Project resembles the weak diffuse scenario much more than the localized strong scenario, which underscores the extent of the power problem for many studies. Possible solutions to the power problem include increasing the sample size, using less stringent thresholds, or focusing on a region-of-interest. However, these approaches are not always feasible and some have major drawbacks. The most prominent solutions that may help address the power problem include model-based (multivariate) prediction methods and meta-analyses with related synthesis-oriented approaches.

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          Most cited references53

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          A positive-negative mode of population covariation links brain connectivity, demographics and behavior

          We investigated the relationship between individual subjects’ functional connectomes and 280 behavioral and demographic measures, in a single holistic multivariate analysis relating imaging to non-imaging data from 461 subjects in the Human Connectome Project. We identified one strong mode of population co-variation; subjects were predominantly spread along a single “positive-negative” axis, linking lifestyle, demographic and psychometric measures to each other and to a specific pattern of brain connectivity.
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            Scanning the horizon: towards transparent and reproducible neuroimaging research

            Functional neuroimaging techniques have transformed our ability to probe the neurobiological basis of behaviour and are increasingly being applied by the wider neuroscience community. However, concerns have recently been raised that the conclusions that are drawn from some human neuroimaging studies are either spurious or
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              Multiple Hypothesis Testing

              J. Shaffer (1995)
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                Author and article information

                Contributors
                Role: ConceptualizationRole: Formal analysisRole: SoftwareRole: VisualizationRole: Writing – original draftRole: Writing – review & editing
                Role: ConceptualizationRole: MethodologyRole: SupervisionRole: Writing – review & editing
                Role: ConceptualizationRole: Formal analysisRole: Funding acquisitionRole: MethodologyRole: SoftwareRole: SupervisionRole: VisualizationRole: Writing – original draftRole: Writing – review & editing
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, CA USA )
                1932-6203
                20 November 2017
                2017
                : 12
                : 11
                : e0184923
                Affiliations
                [1 ] Department of Clinical Psychology, University of Amsterdam, Amsterdam, Netherlands
                [2 ] Department of Psychology and Neuroscience, University of Colorado at Boulder, Boulder, Colorado, United States of America
                [3 ] Department of Psychology, University of Texas at Austin, Austin, Texas, United States of America
                University College London, UNITED KINGDOM
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                Author information
                http://orcid.org/0000-0001-8555-8158
                Article
                PONE-D-17-03459
                10.1371/journal.pone.0184923
                5695788
                29155843
                0b3c6950-9104-4222-b7dc-d59f11e39d80
                © 2017 Cremers et al

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 26 January 2017
                : 1 September 2017
                Page count
                Figures: 4, Tables: 0, Pages: 20
                Funding
                Funded by: funder-id http://dx.doi.org/10.13039/100000002, National Institutes of Health;
                Award ID: R01MH096906
                Award Recipient :
                Funded by: funder-id http://dx.doi.org/10.13039/100000002, National Institutes of Health;
                Award ID: R01DA035484
                Award Recipient :
                The Data analyzed in section 3.2 were provided [in part] by the Human Connectome Project, WU-Minn Consortium (Principal Investigators: David Van Essen and Kamil Ugurbil; 1U54MH091657) funded by the 16 NIH Institutes and Centers that support the NIH Blueprint for Neuroscience Research; and by the McDonnell Center for Systems Neuroscience at Washington University. This work was supported by National institute of Health ( https://grants.nih.gov/grants/about_grants.htm) award R01MH096906 to TY and R01DA035484 to T.D.W.
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                The third-party data underlying this study are available from the Human Connectome Project. The data set can be accessed in the same manner as the authors by registering on http://www.humanconnectome.org/data/.

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