Comparing Methods for Mass Univariate Analyses of Human EEG: Empirical Data and Simulations

比较用于大规模单变量分析人类脑电图的方法:实证数据和模拟

阅读:1

Abstract

Electroencephalography (EEG) is a widely used method for investigating human brain dynamics. However, EEG analyses are frequently conducted with limited a priori knowledge regarding locations or latencies of meaningful statistical effects. This makes it difficult for researchers to form regions of interest (ROIs), which are then analyzed using traditional statistical models such as analysis of variance. In addition, exploratory studies, or studies interested in determining the exact temporal and spatial extent of a predicted effect may aim to examine many sensor locations and time points, often jointly. To address this, mass univariate analyses have become a valuable complement to ROI-based approaches. These methods attempt to correct for multiple comparisons while mitigating the risk of false positives and false negatives, thus enabling statistical inference in high-dimensional EEG data. Here, we review and evaluate different approaches for delineating spatial and temporal effect boundaries in three different datasets, focusing on within-subjects comparisons. Specifically, we focus on permutation-based approaches and their Bayesian alternatives to address condition differences in i) steady-state evoked responses, ii) event-related potentials, and iii) time-frequency data. Overall, simulation results indicate that cluster-based permutation tests provide a relatively liberal approach to correct for multiple comparisons across domains, with high sensitivity for detecting large effects. In contrast, the permutation-based t (max) procedure yields the most conservative method across datasets. Bayesian approaches inherently are continuous in nature and thus strongly depend on the selection of thresholds for when support for a hypothesis is considered meaningful.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。