Providing Evidence for the Null Hypothesis in Functional Magnetic Resonance Imaging Using Group-Level Bayesian Inference. / Masharipov, Ruslan; Knyazeva, Irina; Nikolaev, Yaroslav; Korotkov, Alexander; Didur, Michael; Cherednichenko, Denis; Kireev, Maxim.
In: Frontiers in Neuroinformatics, Vol. 15, 738342, 02.12.2021.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Providing Evidence for the Null Hypothesis in Functional Magnetic Resonance Imaging Using Group-Level Bayesian Inference
AU - Masharipov, Ruslan
AU - Knyazeva, Irina
AU - Nikolaev, Yaroslav
AU - Korotkov, Alexander
AU - Didur, Michael
AU - Cherednichenko, Denis
AU - Kireev, Maxim
N1 - Publisher Copyright: Copyright © 2021 Masharipov, Knyazeva, Nikolaev, Korotkov, Didur, Cherednichenko and Kireev.
PY - 2021/12/2
Y1 - 2021/12/2
N2 - Classical null hypothesis significance testing is limited to the rejection of the point-null hypothesis; it does not allow the interpretation of non-significant results. This leads to a bias against the null hypothesis. Herein, we discuss statistical approaches to ‘null effect’ assessment focusing on the Bayesian parameter inference (BPI). Although Bayesian methods have been theoretically elaborated and implemented in common neuroimaging software packages, they are not widely used for ‘null effect’ assessment. BPI considers the posterior probability of finding the effect within or outside the region of practical equivalence to the null value. It can be used to find both ‘activated/deactivated’ and ‘not activated’ voxels or to indicate that the obtained data are not sufficient using a single decision rule. It also allows to evaluate the data as the sample size increases and decide to stop the experiment if the obtained data are sufficient to make a confident inference. To demonstrate the advantages of using BPI for fMRI data group analysis, we compare it with classical null hypothesis significance testing on empirical data. We also use simulated data to show how BPI performs under different effect sizes, noise levels, noise distributions and sample sizes. Finally, we consider the problem of defining the region of practical equivalence for BPI and discuss possible applications of BPI in fMRI studies. To facilitate ‘null effect’ assessment for fMRI practitioners, we provide Statistical Parametric Mapping 12 based toolbox for Bayesian inference.
AB - Classical null hypothesis significance testing is limited to the rejection of the point-null hypothesis; it does not allow the interpretation of non-significant results. This leads to a bias against the null hypothesis. Herein, we discuss statistical approaches to ‘null effect’ assessment focusing on the Bayesian parameter inference (BPI). Although Bayesian methods have been theoretically elaborated and implemented in common neuroimaging software packages, they are not widely used for ‘null effect’ assessment. BPI considers the posterior probability of finding the effect within or outside the region of practical equivalence to the null value. It can be used to find both ‘activated/deactivated’ and ‘not activated’ voxels or to indicate that the obtained data are not sufficient using a single decision rule. It also allows to evaluate the data as the sample size increases and decide to stop the experiment if the obtained data are sufficient to make a confident inference. To demonstrate the advantages of using BPI for fMRI data group analysis, we compare it with classical null hypothesis significance testing on empirical data. We also use simulated data to show how BPI performs under different effect sizes, noise levels, noise distributions and sample sizes. Finally, we consider the problem of defining the region of practical equivalence for BPI and discuss possible applications of BPI in fMRI studies. To facilitate ‘null effect’ assessment for fMRI practitioners, we provide Statistical Parametric Mapping 12 based toolbox for Bayesian inference.
KW - Bayesian analyses
KW - fMRI
KW - human brain
KW - null results
KW - statistical parametric mapping
UR - http://www.scopus.com/inward/record.url?scp=85121454706&partnerID=8YFLogxK
U2 - 10.3389/fninf.2021.738342
DO - 10.3389/fninf.2021.738342
M3 - Article
AN - SCOPUS:85121454706
VL - 15
JO - Frontiers in Neuroinformatics
JF - Frontiers in Neuroinformatics
SN - 1662-5196
M1 - 738342
ER -
ID: 92287421