Data-driven inference of brain dynamical states from the r-spectrum of correlation matrices
Abstract
We present a data-driven framework to characterize large-scale brain dynamical states directly from correlation matrices at the single-subject level. By treating correlation thresholding as a percolation-like probe of connectivity, the approach tracks multiple cluster- and network-level observables and identifies a characteristic percolation threshold, rc, at which these signatures converge. We use $r_c$ as an operational and physically interpretable descriptor of large-scale brain dynamical sta...
Description / Details
We present a data-driven framework to characterize large-scale brain dynamical states directly from correlation matrices at the single-subject level. By treating correlation thresholding as a percolation-like probe of connectivity, the approach tracks multiple cluster- and network-level observables and identifies a characteristic percolation threshold, rc, at which these signatures converge. We use as an operational and physically interpretable descriptor of large-scale brain dynamical state. Applied to resting-state fMRI data from a large cohort of healthy individuals (N = 996), the method yields stable, subject-specific estimates that covary systematically with established dynamical indicators such as temporal autocorrelations. Numerical simulations of a whole-brain model with a known critical regime further show that tracks changes in collective dynamics under controlled variations of excitability. By replacing arbitrary threshold selection with a criterion intrinsic to correlation structure, the r-spectra provides a physically grounded approach for comparing brain dynamical states across individuals.
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Jan 7, 2026
Neuroscience
Neuroscience
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