Resting-state functional magnetic resonance imaging (rs-fMRI) has been used to construct functional connectivity (FC) in the brain for the diagnosis and analysis of brain disease. Current studies typically use the Pearson correlation coefficient to construct dynamic FC (dFC) networks, and then use this as a network metric to obtain the necessary features for brain disease diagnosis and analysis. This simple observational approach makes it difficult to extract potential high-level FC features from the representations, and also ignores the rich information on spatial and temporal variability in FC.
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