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Rousselet, G. A.

Publications and source records attributed to Rousselet, G. A..

8 recordsLinked to original sources

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

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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Data-driven estimates of the reproducibility of univariate BWAS are biased.

Recent studies have used big neuroimaging datasets to answer an important question: how many subjects are required for reproducible brain-wide association studies? These data-driven approaches could be considered a framework for testing the reproducibility of several neuroimaging models and measures. Here we test part of this framework, namely estimates of statistical errors of univariate brain-behaviour associations obtained from resampling large datasets with replacement. We demonstrate that reported estimates of statistical errors are largely a consequence of bias introduced by random effects when sampling with replacement close to the full sample size. We show that future meta-analyses can largely avoid these biases by only resampling up to 10% of the full sample size. We discuss implications that reproducing mass-univariate association studies requires tens-of-thousands of participants, urging researchers to adopt other methodological approaches.

neuroscience↗

Can Prediction Error Explain Predictability Effects on the N1 during Picture-Word Verification?

Do early effects of predictability in visual word recognition reflect prediction error? Electrophysiological research investigating word processing has demonstrated predictability effects in the N1, or first negative component of the event-related potential (ERP). However, findings regarding the magnitude of effects and potential interactions of predictability with lexical variables have been inconsistent. Moreover, past studies have typically used categorical designs with relatively small samples and relied on by-participant analyses. Nevertheless, reports have generally shown that predicted words elicit less negative-going (i.e., lower amplitude) N1s, a pattern consistent with a simple predictive coding account. In our preregistered study, we tested this account via the interaction between prediction magnitude and certainty. A picture-word verification paradigm was implemented in which pictures were followed by tightly matched picture-congruent or picture-incongruent written nouns. The predictability of target (picture-congruent) nouns was manipulated continuously based on norms of association between a picture and its name. ERPs from 68 participants revealed a pattern of effects opposite to that expected under a simple predictive coding framework.

neuroscience↗

Robust linear modelling in ElectroEncephaloGraphy can be obtained using single weights reflecting each single trials' dynamics

Being able to remove or weigh down the influence of outlier data is desirable for any statistical models. While Magnetic and ElectroEncephaloGraphic (MEEG) data are often averaged across trials per condition, it is becoming common practice to use information from all trials to build statistical linear models. Individual trials can, however, have considerable weight and thus bias inferential results (effect sizes as well as thresholded t/F/p maps). Here, rather than looking for univariate outliers, defined independently at each measurement point, we apply the principal component projection (PCP) method at each channel, deriving a single weight per trial at each channel independently. Using both synthetic data and open EEG data, we show (1) that PCP is efficient at detecting a large variety of outlying trials; (2) how PCP-based weights can be implemented in the context of the general linear model (GLM) with accurate control of type 1 family-wise error rate; and (3) that our PCP-based Weighted Least Square (WLS) approach increases the statistical power of group analyses as well as a much slower Iterative Reweighted Least Squares (IRLS), although the weighting scheme is markedly different. Together, our results show that WLS based on PCP weights derived from whole trial profiles is an efficient method to weigh down the influence of outlier EEG data in linear models. Data availabilityall data used are publicly available (CC0), all code (simulations and data analyzes) is also available online in the LIMO MEEG GitHub repository (MIT license).

neuroscience↗

Reaction times and other skewed distributions: problems with the mean and the median

To summarise skewed (asymmetric) distributions, such as reaction times, typically the mean or the median are used as measures of central tendency. Using the mean might seem surprising, given that it provides a poor measure of central tendency for skewed distributions, whereas the median provides a better indication of the location of the bulk of the observations. However, the sample median is biased: with small sample sizes, it tends to overestimate the population median. This is not the case for the mean. Based on this observation, Miller (1988) concluded that \"sample medians must not be used to compare reaction times across experimental conditions when there are unequal numbers of trials in the conditions.\" Here we replicate and extend Miller (1988), and demonstrate that his conclusion was ill-advised for several reasons. First, the medians bias can be corrected using a percentile bootstrap bias correction. Second, a careful examination of the sampling distributions reveals that the sample median is median unbiased, whereas the mean is median biased when dealing with skewed distributions. That is, on average the sample mean estimates the population mean, but typically this is not the case. In addition, simulations of false and true positives in various situations show that no method dominates. Crucially, neither the mean nor the median are sufficient or even necessary to compare skewed distributions. Different questions require different methods and it would be unwise to use the mean or the median in all situations. Better tools are available to get a deeper understanding of how distributions differ: we illustrate a powerful alternative that relies on quantile estimation. All the code and data to reproduce the figures and analyses in the article are available online.

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Neural Processing of the Same, Behaviourally Relevant Face Features is Delayed by 40 ms in Healthy Ageing

Fast and accurate face processing is critical for everyday social interactions, but it declines and becomes delayed with age, as measured by both neural and behavioural responses. Here, we addressed the critical challenge of understanding how ageing changes neural information processing mechanisms to delay behaviour. Young (20-36 years) and older (60-86 years) adults performed the basic social interaction task detecting a face vs. noise while we recorded their electroencephalogram (EEG). In each participant, using a new information theoretic framework we reconstructed the features supporting face detection behaviour, and also where, when and how EEG activity represents them. We found that occipital-temporal pathway activity dynamically represents the eyes of the face images for behaviour [~]170 ms post-stimulus, with a 40 ms delay in older adults that underlies their 200 ms behavioural deficit of slower reaction times. Our results therefore demonstrate how ageing can change neural information processing mechanisms that underlie behavioural slow down.\n\nAuthor summaryOlder adults are consistently slower than young adults in a variety of behavioural perceptual tasks. So far, it has been unclear if the underlying cause of the behavioural delay relates to attentional or perceptual differences in encoding visual information, or slower neural processing speed, or other neural factors. Our study addresses these questions by showing that in a basic social interaction task (discriminating faces from noise), young and older adults encoded the same visual information (eyes of the face) to perform the task. Moreover, early brain activity (within 200 ms following stimulus onset) encoded the same visual information (again, eyes of the face) in both groups, but was delayed and weaker in older adults. These early delays in information encoding were directly related to the observed behavioural slowing in older adults, showing that differences in early perceptual brain processes can contribute to the motor response.

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A guide to robust statistical methods in neuroscience

There is a vast array of new and improved methods for comparing groups and studying associations that offer the potential for substantially increasing power, providing improved control over the probability of a Type I error, and yielding a deeper and more nuanced understanding of neuroscience data. These new techniques effectively deal with four insights into when and why conventional methods can be unsatisfactory. But for the non-statistician, the vast array of new and improved techniques for comparing groups and studying associations can seem daunting, simply because there are so many new methods that are now available. The paper briefly reviews when and why conventional methods can have relatively low power and yield misleading results. The main goal is to suggest some general guidelines regarding when, how and why certain modern techniques might be used.

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Beyond differences in means: robust graphical methods to compare two groups in neuroscience

If many changes are necessary to improve the quality of neuroscience research, one relatively simple step could have great pay-offs: to promote the adoption of detailed graphical methods, combined with robust inferential statistics. Here we illustrate how such methods can lead to a much more detailed understanding of group differences than bar graphs and t-tests on means. To complement the neuroscientists toolbox, we present two powerful tools that can help us understand how groups of observations differ: the shift function and the difference asymmetry function. These tools can be combined with detailed visualisations to provide complementary perspectives about the data. We provide implementations in R and Matlab of the graphical tools, and all the examples in the article can be reproduced using R scripts.

neuroscience↗