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Family Wise Error Correction Fmri

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Family Wise Error Rate Correction

HealthSNPSparcleSRAStructureTaxonomyToolKitToolKitAllToolKitBookToolKitBookghUniGeneSearch termSearch Advanced Journal list Help Journal ListHHS Author familywise error correction ManuscriptsPMC4214144 Neuroimage. Author manuscript; available in PMC 2014 Oct 30.Published in final edited form cluster-extent based thresholding in fmri analyses: pitfalls and recommendations as:Neuroimage. 2014 May 1; 91: 412–419. Published online 2014 Jan 8. doi:  10.1016/j.neuroimage.2013.12.058PMCID: PMC4214144NIHMSID: NIHMS636029Cluster-extent based thresholding in fMRI analyses: Pitfalls and recommendationsChoong-Wan

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Woo, Anjali Krishnan, and Tor D. Wager*Department of Psychology and Neuroscience, University of Colorado Boulder, USA. Institute of Cognitive Science, University of Colorado Boulder, USA*Corresponding author at: Department of Psychology and Neuroscience, University of Colorado Boulder, 345 UCB, Boulder, CO 80309-0345, USA. Email: udE.odaroloC@regaW.roT (T.D.Wager)Author information

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► Copyright and License information ►Copyright notice and DisclaimerThe publisher's final edited version of this article is available at NeuroimageSee other articles in PMC that cite the published article.AbstractCluster-extent based thresholding is currently the most popular method for multiple comparisons correction of statistical maps in neuroimaging studies, due to its high sensitivity to weak and diffuse signals. However, cluster-extent based thresholding provides low spatial specificity; researchers can only infer that there is signal somewhere within a significant cluster and cannot make inferences about the statistical significance of specific locations within the cluster. This poses a particular problem when one uses a liberal cluster-defining primary threshold (i.e., higher p-values), which often produces large clusters spanning multiple anatomical regions. In such cases, it is impossible to reliably infer which anatomical regions show true effects. From a survey of 8

may be challenged and removed. (June 2016) (Learn how and when to remove this template message) In statistics, family-wise error rate (FWER) is the can parametric statistical methods be trusted for fmri based group studies? probability of making one or more false discoveries, or type I

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errors, among all the hypotheses when performing multiple hypotheses tests. Contents 1 History 2 Background 2.1 Classification family wise error rate post hoc of multiple hypothesis tests 3 Definition 4 Controlling procedures 4.1 The Bonferroni procedure 4.2 The Šidák procedure 4.3 Tukey's procedure 4.4 Holm's step-down procedure (1979) 4.5 Hochberg's https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4214144/ step-up procedure 4.6 Dunnett's correction 4.7 Scheffé's method 4.8 Resampling procedures 5 Alternative approaches 6 References History[edit] Tukey coined the terms experimentwise error rate and "error rate per-experiment" to indicate error rates that the researcher could use as a control level in a multiple hypothesis experiment.[citation needed] Background[edit] Within the statistical framework, there are several definitions https://en.wikipedia.org/wiki/Family-wise_error_rate for the term "family": Hochberg & Tamhane defined "family" in 1987 as "any collection of inferences for which it is meaningful to take into account some combined measure of error".[1][pageneeded] According to Cox in 1982, a set of inferences should be regarded a family:[citation needed] To take into account the selection effect due to data dredging To ensure simultaneous correctness of a set of inferences as to guarantee a correct overall decision To summarize, a family could best be defined by the potential selective inference that is being faced: A family is the smallest set of items of inference in an analysis, interchangeable about their meaning for the goal of research, from which selection of results for action, presentation or highlighting could be made (Yoav Benjamini).[citation needed] Classification of multiple hypothesis tests[edit] Main article: Classification of multiple hypothesis tests The following table defines various errors committed when testing multiple null hypotheses. Suppose we have a number m of multiple null hypotheses, denoted by: H1,H2

My Basket My Account Social Cognitive & Affective Neurosci About This Journal Contact This Journal Subscriptions View Current Issue (Volume 11 Issue 10 October 2016) Archive Search Oxford Journals Medicine & Health Social http://scan.oxfordjournals.org/content/4/4/417.full Cognitive & Affective Neurosci Volume 4 Issue 4 Pp. 417-422. The principled control of false positives in neuroimaging Craig M. Bennett1, George L. Wolford2 and Michael B. Miller1 1Department of Psychology, University of California, Santa Barbara, California, 93106 and 2Department of Psychological and Brain Sciences, Moore Hall, Dartmouth College, Hanover, New Hampshire 03755, USA Correspondence should be addressed to Craig M. Bennett, Department of Psychology, University of California, Santa Barbara, Santa Barbara, CA 93106, wise error USA. E-mail: bennett{at}psych.ucsb.edu Received November 7, 2009. Accepted December 7, 2009.  Next Section Abstract An incredible amount of data is generated in the course of a functional neuroimaging experiment. The quantity of data gives us improved temporal and spatial resolution with which to evaluate our results. It also creates a staggering multiple testing problem. A number of methods have been created that address the multiple testing problem in neuroimaging in a principled fashion. These family wise error methods place limits on either the familywise error rate (FWER) or the false discovery rate (FDR) of the results. These principled approaches are well established in the literature and are known to properly limit the amount of false positives across the whole brain. However, a minority of papers are still published every month using methods that are improperly corrected for the number of tests conducted. These latter methods place limits on the voxelwise probability of a false positive and yield no information on the global rate of false positives in the results. In this commentary, we argue in favor of a principled approach to the multiple testing problem—one that places appropriate limits on the rate of false positives across the whole brain gives readers the information they need to properly evaluate the results. Key words fMRI statistics FDR FWER The struggle between the appropriate treatment of false positives and false negatives is a fine line that every scientist must walk. If our criteria are too conservative, we will not have the power to detect meaningful results. If our thresholds are too liberal, our results will become contaminated by an excess of false positives. Ideally, we hope to maximize the number of true positives (hits) while minimizing false reports. It is a statistical necessity that we must adapt our threshold c

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