Evidence map›Paper›PMID 39617724›Full record

ArticleThe European journal of neuroscience2025

Using cluster-based permutation tests to estimate MEG/EEG onsets: How bad is it?

Guillaume A Rousselet

Abstract read
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  9. Brain responses vary in duration-modeling strategies and challenges.Imaging neuroscience (Cambridge, Mass.) · 2025
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

1 author.

Guillaume A RousseletSchool of Psychology and Neuroscience, College of Medical, Veterinary and Life, Sciences, University of Glasgow, Glasgow, UK.ORCID 0000-0003-0006-8729

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

ElectroencephalographyMagnetoencephalographyBrainCluster AnalysisComputer SimulationData Interpretation, StatisticalHumanscluster inferencecorrection for multiple comparisonsEEGfalse discovery ratefamilywise error rateMEGMonte Carlo simulationonset estimationpermutation

Identifiers

PMID39617724
PMCPMC11670281

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Registered trials

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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.