Key result
Cluster-based permutation tests show positive bias but perform well versus point-wise methods for MEG/EEG onsets.
Why the study?
Cluster-based permutation tests lack point-wise error control and may yield biased onset estimates, but previous simulations lacked comparisons to other methods.
Cluster-based permutation tests for MEG/EEG onset estimation show positive bias but perform comparably well against other point-wise p-value methods, and bias can be reduced using binary segmentation.
Answers are grounded in this paper and cite their sources.
Cluster-based tests' positive bias warrants caution in MEG/EEG onset timing; extends point-wise method comparisons with bias-variability data.
Localising effects in space, time and other dimensions is a fundamental goal of magneto- and electro-encephalography (EEG) research. A popular exploratory approach applies mass-univariate statistics followed by cluster-sum inferences, an effective way to correct for multiple comparisons while preserving high statistical power by pooling together neighbouring effects. Yet, these cluster-based methods have an important limitation: each cluster is associated with a unique p value, such that there is no error control at individual time points, and one must be cautious about interpreting when and where effects start and end. Sassenhagen & Draschkow (2019) provided an important reminder of this limitation. They also reported results from a simulation, suggesting that onsets estimated from EEG data are both positively biased and very variable. However, the simulation lacked comparisons to other methods. Here I report such comparisons in a new simulation, replicating the positive bias of the cluster-sum method, but also demonstrating that it performs relatively well, in terms of bias and variability, compared to other methods that provide point-wise p values: two methods that control the false discovery rate, and two methods that control the family-wise error rate (cluster-depth and maximum statistic methods). I also present several strategies to reduce estimation bias, including group calibration, group comparison, and using binary segmentation, a simple change point detection algorithm that outperformed mass-univariate methods in simulations. Finally, I demonstrate how to generate onset hierarchical bootstrap confidence intervals that integrate variability over trials and participants, a substantial improvement over standard group approaches that ignore measurement uncertainty.
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Guillaume A. Rousselet (2023) studied MEG/EEG data analysis. Cluster-based permutation tests vs. Other statistical methods (FDR, cluster-depth, maximum statistic, binary segmentation) was evaluated on Estimation bias and variability of MEG/EEG onsets. Cluster-based permutation tests for estimating MEG/EEG onsets showed positive bias but performed relatively well in terms of bias and variability compared to other point-wise p-value methods.
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