ArticleThe European journal of neuroscience2025
Using cluster-based permutation tests to estimate MEG/EEG onsets: How bad is it?
Article in The European journal of neuroscience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.
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Who cites it
10 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Heartbeat-Evoked Responses in M/EEG: A Systematic Review of Methods With Suggestions for Analysis and Reporting.Psychophysiology · 2026Pooled it
- Article
- Comparing Methods for Mass Univariate Analyses of Human EEG: Empirical Data and Simulations.bioRxiv : the preprint server for biology · 2025Article
- Mapping EEG Metrics to Human Affective and Cognitive Models: An Interdisciplinary Scoping Review from a Cognitive Neuroscience Perspective.Biomimetics (Basel, Switzerland) · 2025Review
- Using Simulations to Explore Sampling Distributions: An Antidote to Hasty and Extravagant Inferences.eNeuro · 2025Article
- Neural dynamics of proactive and reactive cognitive control in medial and lateral prefrontal cortex.iScience · 2025Article
- Discrete Repetition Effects for Visual Words Compared to Faces and Animals, but No Modulation by Expectation: An Event-Related Potential Study.The European journal of neuroscience · 2025Article
- Using cluster-based permutation tests to estimate MEG/EEG onsets: How bad is it?The European journal of neuroscience · 2025Article
- Brain responses vary in duration-modeling strategies and challenges.Imaging neuroscience (Cambridge, Mass.) · 2025Article
- Article
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Authors and funding
1 author.
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Abstract
Localising effects in space, time and other dimensions is a fundamental goal of magneto- and electroencephalography (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 timepoints, and one must be cautious about interpreting when and where effects start and end. Sassenhagen and 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 pointwise p-values: two methods that control the false discovery rate and two methods that control the familywise 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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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.