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      Non‐parametric combination and related permutation tests for neuroimaging

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          Abstract

          In this work, we show how permutation methods can be applied to combination analyses such as those that include multiple imaging modalities, multiple data acquisitions of the same modality, or simply multiple hypotheses on the same data. Using the well‐known definition of union‐intersection tests and closed testing procedures, we use synchronized permutations to correct for such multiplicity of tests, allowing flexibility to integrate imaging data with different spatial resolutions, surface and/or volume‐based representations of the brain, including non‐imaging data. For the problem of joint inference, we propose and evaluate a modification of the recently introduced non‐parametric combination (NPC) methodology, such that instead of a two‐phase algorithm and large data storage requirements, the inference can be performed in a single phase, with reasonable computational demands. The method compares favorably to classical multivariate tests (such as MANCOVA), even when the latter is assessed using permutations. We also evaluate, in the context of permutation tests, various combining methods that have been proposed in the past decades, and identify those that provide the best control over error rate and power across a range of situations. We show that one of these, the method of Tippett, provides a link between correction for the multiplicity of tests and their combination. Finally, we discuss how the correction can solve certain problems of multiple comparisons in one‐way ANOVA designs, and how the combination is distinguished from conjunctions, even though both can be assessed using permutation tests. We also provide a common algorithm that accommodates combination and correction. Hum Brain Mapp 37:1486‐1511, 2016. © 2016 Wiley Periodicals, Inc.

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          Statistical methods for assessing agreement between two methods of clinical measurement.

          In clinical measurement comparison of a new measurement technique with an established one is often needed to see whether they agree sufficiently for the new to replace the old. Such investigations are often analysed inappropriately, notably by using correlation coefficients. The use of correlation is misleading. An alternative approach, based on graphical techniques and simple calculations, is described, together with the relation between this analysis and the assessment of repeatability.
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            Combining probability from independent tests: the weighted Z-method is superior to Fisher's approach.

            The most commonly used method in evolutionary biology for combining information across multiple tests of the same null hypothesis is Fisher's combined probability test. This note shows that an alternative method called the weighted Z-test has more power and more precision than does Fisher's test. Furthermore, in contrast to some statements in the literature, the weighted Z-method is superior to the unweighted Z-transform approach. The results in this note show that, when combining P-values from multiple tests of the same hypothesis, the weighted Z-method should be preferred.
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              Comparing functional (PET) images: the assessment of significant change.

              Statistical parametric maps (SPMs) are potentially powerful ways of localizing differences in regional cerebral activity. This potential is limited by uncertainties in assessing the significance of these maps. In this report, we describe an approach that may partially resolve this issue. A distinction is made between using SPMs as images of change significance and using them to identify foci of significant change. In the first case, the SPM can be reported nonselectively as a single mathematical object with its omnibus significance. Alternatively, the SPM constitutes a large number of repeated measures over the brain. To reject the null hypothesis, that no change has occurred at a specific location, a threshold adjustment must be made that accounts for the large number of comparisons made. This adjustment is shown to depend on the SPM's smoothness. Smoothness can be determined empirically and be used to calculate a threshold required to identify significant foci. The approach models the SPM as a stationary stochastic process. The theory and applications are illustrated using uniform phantom images and data from a verbal fluency activation study of four normal subjects.
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                Author and article information

                Journal
                Hum Brain Mapp
                Hum Brain Mapp
                10.1002/(ISSN)1097-0193
                HBM
                Human Brain Mapping
                John Wiley and Sons Inc. (Hoboken )
                1065-9471
                1097-0193
                05 February 2016
                April 2016
                : 37
                : 4 ( doiID: 10.1002/hbm.v37.4 )
                : 1486-1511
                Affiliations
                [ 1 ] Oxford Centre for Functional MRI of the BrainUniversity of Oxford OxfordUnited Kingdom
                [ 2 ]Clinical Research and Imaging Centre, University of Bristol BristolUnited Kingdom
                [ 3 ] Department of Statistics & Warwick Manufacturing GroupUniversity of Warwick CoventryUnited Kingdom
                Author notes
                [*] [* ]Correspondence to: Anderson M. Winkler, Oxford Centre for Functional MRI of the Brain, University of Oxford, Oxford, United Kingdom. E‐mail: winkler@ 123456fmrib.ox.ac.uk
                Author information
                http://orcid.org/0000-0002-4169-9781
                Article
                HBM23115
                10.1002/hbm.23115
                4783210
                26848101
                60646329-4418-4205-ad65-9cc88a3f04fb
                © 2016 The Authors Human Brain Mapping Published by Wiley Periodicals, Inc.

                This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 05 August 2015
                : 15 December 2015
                : 03 January 2016
                Page count
                Pages: 26
                Funding
                Funded by: Brazilian National Research Council (CNPq)
                Award ID: 211534/2013‐7
                Funded by: MRC
                Award ID: G0900908
                Funded by: NIH
                Award ID: R01 EB015611‐01, NS41287
                Funded by: Wellcome Trust
                Award ID: 100309/Z/12/Z, 098369/Z/12/Z
                Funded by: Marie Curie Initial Training Network
                Award ID: MC‐ITN‐238593
                Funded by: GlaxoSmithKline plc, The Dr. Hadwen Trust for Humane Research, and the Barrow Neurological Institute.
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                hbm23115
                April 2016
                Converter:WILEY_ML3GV2_TO_NLMPMC version:4.9.1 mode:remove_FC converted:23.06.2016

                Neurology
                permutation tests,non‐parametric combination,multiple testing,conjunctions,general linear model

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