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      Robust Spatial Extent Inference with a Semiparametric Bootstrap Joint Testing Procedure

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          Abstract

          Spatial extent inference (SEI) is widely used across neuroimaging modalities to study brain-phenotype associations that inform our understanding of disease. Recent studies have shown that Gaussian random field (GRF) based tools can have inflated family-wise error rates (FWERs). This has led to fervent discussion as to which preprocessing steps are necessary to control the FWER using GRF-based SEI. The failure of GRF-based methods is due to unrealistic assumptions about the covariance function of the imaging data. The permutation procedure is the most robust SEI tool because it estimates the covariance function from the imaging data. However, the permutation procedure can fail because its assumption of exchangeability is violated in many imaging modalities. Here, we propose the (semi-) parametric bootstrap joint (PBJ; sPBJ) testing procedures that are designed for SEI of multilevel imaging data. The sPBJ procedure uses a robust estimate of the covariance function, which yields consistent estimates of standard errors, even if the covariance model is misspecified. We use our methods to study the association between performance and executive functioning in a working fMRI study. The sPBJ procedure is robust to variance misspecification and maintains nominal FWER in small samples, in contrast to the GRF methods. The sPBJ also has equal or superior power to the PBJ and permutation procedures. We provide an R package https://github.com/simonvandekar/pbj to perform inference using the PBJ and sPBJ procedures

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          Most cited references25

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          Some heteroskedasticity-consistent covariance matrix estimators with improved finite sample properties

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            The development of human functional brain networks.

            Recent advances in MRI technology have enabled precise measurements of correlated activity throughout the brain, leading to the first comprehensive descriptions of functional brain networks in humans. This article reviews the growing literature on the development of functional networks, from infancy through adolescence, as measured by resting-state functional connectivity MRI. We note several limitations of traditional approaches to describing brain networks and describe a powerful framework for analyzing networks, called graph theory. We argue that characterization of the development of brain systems (e.g., the default mode network) should be comprehensive, considering not only relationships within a given system, but also how these relationships are situated within wider network contexts. We note that, despite substantial reorganization of functional connectivity, several large-scale network properties appear to be preserved across development, suggesting that functional brain networks, even in children, are organized in manners similar to other complex systems. 2010 Elsevier Inc. All rights reserved.
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              Neuroimaging of the Philadelphia neurodevelopmental cohort.

              The Philadelphia Neurodevelopmental Cohort (PNC) is a large-scale, NIMH funded initiative to understand how brain maturation mediates cognitive development and vulnerability to psychiatric illness, and understand how genetics impacts this process. As part of this study, 1445 adolescents ages 8-21 at enrollment underwent multimodal neuroimaging. Here, we highlight the conceptual basis for the effort, the study design, and the measures available in the dataset. We focus on neuroimaging measures obtained, including T1-weighted structural neuroimaging, diffusion tensor imaging, perfusion neuroimaging using arterial spin labeling, functional imaging tasks of working memory and emotion identification, and resting state imaging of functional connectivity. Furthermore, we provide characteristics regarding the final sample acquired. Finally, we describe mechanisms in place for data sharing that will allow the PNC to become a freely available public resource to advance our understanding of normal and pathological brain development. © 2013 Elsevier Inc. All rights reserved.
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                Author and article information

                Journal
                22 August 2018
                Article
                1808.07449
                b6e1c431-78af-4998-b29d-33b2e9ebd8ea

                http://arxiv.org/licenses/nonexclusive-distrib/1.0/

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