Abstract

Much relevant information about activations and artifacts in a functional magnetic resonance imaging (fMRI) dataset can be obtained from an exploratory cluster analysis. In contrast to testing the significance of the measured experimental effect for a given model, unsupervised pattern recognition techniques, such as fuzzy clustering, often find unexpected behavior in addition to expected activations, allowing the exploitation of this element of surprise. The many artifact clusters often discovered might aid the experimenter in deciding whether the dataset is usable, whether some additional preprocessing step is required, or whether the one used has introduced spurious effects. However, clustering alone does not complete the analysis because the membership values that are generated are not indicative of the level of statistical significance with respect to the cluster activation patterns (centroids). This is of particular importance for fMRI datasets for which most time-series are “noise”, with no activation patterns. We propose that an initial partition step should precede the clustering step. Only time-series that meet a certain statistical criterion (using a scaled version of Fisher’s g-order statistic) are selected for clustering; this typically represents <5% of the whole brain region. The purpose of clustering is to generate a set of cluster centers that are the possible activation patterns; these are used in forming a linear model of all the time-series. The model parameter is tested for significance in both the time and frequency domains. We present a novel method of conducting these tests, which limits the number of false positives. We call the three-step process of initial partition, clustering and the two-domain significance test as exploring regions of interest with cluster analysis (EROICA).

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