ePoster, Bernstein Conference 2024
Enhanced simulations of whole-brain dynamics using hybrid resting-state structural connectomes
- Goethe University, Frankfurt, Germany
- DOI 10.12751/nncn.bc2024.311 (opens in a new tab)
- Computational Neuroscience, Dynamical Systems and
Audio
Abstract
The human brain, composed of billions of neurons and synaptic connections, is an intricate network coordinating a sophisticated balance of excitatory and inhibitory activity between brain regions. The dynamical balance between excitation and inhibition is vital for adjusting neural input/output relationships in cortical networks and regulating the dynamic range of their responses to stimuli. To infer this balance using connectomics, we recently introduced a computational framework based on the Ising model, first developed to explain phase transitions in ferromagnets, and proposed a novel hybrid resting-state structural connectome (rsSC). Here, we show that a generative model based on the Kuramoto phase oscillator can be used to simulate static and dynamic functional connectomes (FC) with rsSC as the coupling weight coefficients, such that the simulated FC well aligns with the observed FC when compared to that simulated with traditional structural connectome. Simulations were performed using the open source framework The Virtual Brain on High Performance Computing infrastructure.
Topics
- human brain, search World Wide
- excitatory and inhibitory activity, search World Wide
- cortical networks, search World Wide
- neural input/output relationships, search World Wide
- Ising model, search World Wide
- hybrid resting-state structural connectome, search World Wide
- Kuramoto phase oscillator, search World Wide
- functional connectomes, search World Wide
- The Virtual Brain, search World Wide
- High Performance Computing, search World Wide
Details
- Citation
- Thanos Manos, Sandra Diaz-Pier, Igor Fortel et al. (2024). Enhanced simulations of whole-brain dynamics using hybrid resting-state structural connectomes. Bernstein Conference 2024. https://doi.org/10.12751/nncn.bc2024.311 (opens in a new tab)