Rest2Visual: Predicting Visually Evoked fMRI from Resting-State Scans
- URL: http://arxiv.org/abs/2509.13612v1
- Date: Wed, 17 Sep 2025 01:08:03 GMT
- Title: Rest2Visual: Predicting Visually Evoked fMRI from Resting-State Scans
- Authors: Chuyang Zhou, Ziao Ji, Daochang Liu, Dongang Wang, Chenyu Wang, Chang Xu,
- Abstract summary: We introduce Rest2Visual, a conditional generative model that predicts visually evoked fMRI (ve-fMRI) from resting-state input and 2D visual stimuli.<n>Our results provide compelling evidence that individualized spontaneous neural activity can be transformed into stimulus-aligned representations.
- Score: 30.743554598059692
- License: http://arxiv.org/licenses/nonexclusive-distrib/1.0/
- Abstract: Understanding how spontaneous brain activity relates to stimulus-driven neural responses is a fundamental challenge in cognitive neuroscience. While task-based functional magnetic resonance imaging (fMRI) captures localized stimulus-evoked brain activation, its acquisition is costly, time-consuming, and difficult to scale across populations. In contrast, resting-state fMRI (rs-fMRI) is task-free and abundant, but lacks direct interpretability. We introduce Rest2Visual, a conditional generative model that predicts visually evoked fMRI (ve-fMRI) from resting-state input and 2D visual stimuli. It follows a volumetric encoder--decoder design, where multiscale 3D features from rs-fMRI are modulated by image embeddings via adaptive normalization, enabling spatially accurate, stimulus-specific activation synthesis. To enable model training, we construct a large-scale triplet dataset from the Natural Scenes Dataset (NSD), aligning each rs-fMRI volume with stimulus images and their corresponding ve-fMRI activation maps. Quantitative evaluation shows that the predicted activations closely match ground truth across standard similarity and representational metrics, and support successful image reconstruction in downstream decoding. Notably, the predicted maps preserve subject-specific structure, demonstrating the model's capacity to generate individualized functional surrogates. Our results provide compelling evidence that individualized spontaneous neural activity can be transformed into stimulus-aligned representations, opening new avenues for scalable, task-free functional brain modeling.
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