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Meysam Hashemi

Publications and source records attributed to Meysam Hashemi.

4 recordsLinked to original sources

Cohort-amortized personalization: navigating the privacy-utility frontier for virtual brain twins

Personalized generative brain models require individual neuroimaging data that privacy constraints and re-identification risk make difficult to share, while per-subject fitting procedures cost hours of compute -- limiting clinical translation and multi-site collaboration. We introduce cohort-amortized personalization (CAP), which replaces data sharing with model sharing: a neural density estimator is trained on simulations from a mechanistic whole-brain model under a low-rank cohort prior, and only the compact estimator is distributed, so new subjects are personalized in seconds on their own data alone. To make this prior both compact and atlas-independent, a cross-atlas autoencoder (CrossCoder) maps connectomes from 20 anatomical atlases into a shared latent space, enabling deployment across sites with heterogeneous atlases. We validate CAP on two cohorts: 21 patients with drug-resistant epilepsy (epileptogenic-zone localization F1=0.56) and 832 subjects from the 1000BRAINS aging cohort (predicted age r=0.44); in both, CAP matches or exceeds per-subject inference with hours-to-seconds speed-up. Because the shared artifact couples a cohort prior to a mechanistic simulator, it can serve as a mechanistic surrogate supporting in-silico experimentation and synthetic-cohort generation without raw-data access -- a governance-audited alternative we term synthetic access, allowing for wider adoption of personalized modeling in more diverse settings.

q-bio.NC

Data-driven mean-field within whole-brain models

Mean-field models provide a link between microscopic neuronal activity and macroscopic brain dynamics. Their derivation depends on simplifying assumptions, such as all-to-all connectivity, limiting their biological realism. To overcome this, we introduce a data-driven framework in which a multi-layer perceptron (MLP) learns the macroscopic dynamics directly from simulations of a network of spiking neurons. The network connection probability serves here as a new parameter, inaccessible to purely analytical treatment, which is validated against ground truth analytical solutions. Through bifurcation analysis on the trained MLP, we demonstrate the existence of new cusp bifurcation that systematically reshapes the system's phase diagram in a degenerate manner with synaptic coupling. By integrating this data-driven mean-field model into a whole-brain computational framework, we show that it extends beyond the macroscopic emergent dynamics generated by the analytical model. For validation, we use simulation-based inference on synthetic functional magnetic resonance imaging (fMRI) data and demonstrate accurate parameter recovery for the novel mean-field model, while the current state-of-the-art models lead to biased estimates. This work presents a flexible and generic framework for building more realistic whole-brain models, bridging the gap between microscale mechanisms and macroscopic brain recordings.

q-bio.NC

Brain Modelling as a Service: The Virtual Brain on EBRAINS

The Virtual Brain (TVB) is now available as open-source cloud ecosystem on EBRAINS, a shared digital research platform for brain science. It offers services for constructing, simulating and analysing brain network models (BNMs) including the TVB network simulator; magnetic resonance imaging (MRI) processing pipelines to extract structural and functional connectomes; multiscale co-simulation of spiking and large-scale networks; a domain specific language for automatic high-performance code generation from user-specified models; simulation-ready BNMs of patients and healthy volunteers; Bayesian inference of epilepsy spread; data and code for mouse brain simulation; and extensive educational material. TVB cloud services facilitate reproducible online collaboration and discovery of data assets, models, and software embedded in scalable and secure workflows, a precondition for research on large cohort data sets, better generalizability and clinical translation.

cs.CE

Effect of the duration of the synaptic activity on a delayed recurrent neuronal loop

A recurrent loop consisting of a single neuron is considered which is influenced by a chemical excitatory delayed synaptic feedback. We show the response of the system is dependent to the duration of the activity of the synapse which is determined by the deactivation time constant of the synapse. We show that loops with slow synapses, those which the effect of the synaptic activation remains for time constants comparable to the period of firing, show more predictable results where the effect of the fast synapses is tightly dependent on the loop delay time. The results are compared to those of the loops with inhibitory synapses and also with electrical synapses.

q-bio.NC