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The empirical replicability of task-based fMRI as a function of sample size
The empirical replicability of task-based fMRI as a function of sample size
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The empirical replicability of task-based fMRI as a function of sample size
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The empirical replicability of task-based fMRI as a function of sample size
The empirical replicability of task-based fMRI as a function of sample size

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The empirical replicability of task-based fMRI as a function of sample size
The empirical replicability of task-based fMRI as a function of sample size
Journal Article

The empirical replicability of task-based fMRI as a function of sample size

2020
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Overview
Replicating results (i.e. obtaining consistent results using a new independent dataset) is an essential part of good science. As replicability has consequences for theories derived from empirical studies, it is of utmost importance to better understand the underlying mechanisms influencing it. A popular tool for non-invasive neuroimaging studies is functional magnetic resonance imaging (fMRI). While the effect of underpowered studies is well documented, the empirical assessment of the interplay between sample size and replicability of results for task-based fMRI studies remains limited. In this work, we extend existing work on this assessment in two ways. Firstly, we use a large database of 1400 subjects performing four types of tasks from the IMAGEN project to subsample a series of independent samples of increasing size. Secondly, replicability is evaluated using a multi-dimensional framework consisting of 3 different measures: (un)conditional test-retest reliability, coherence and stability. We demonstrate not only a positive effect of sample size, but also a trade-off between spatial resolution and replicability. When replicability is assessed voxelwise or when observing small areas of activation, a larger sample size than typically used in fMRI is required to replicate results. On the other hand, when focussing on clusters of voxels, we observe a higher replicability. In addition, we observe variability in the size of clusters of activation between experimental paradigms or contrasts of parameter estimates within these.