Abstract
Human brain activity contains stable, individual-specific features that persist over months to years, forming neurophysiological profiles. Most model-based profiling approaches use participant labels or supervised objectives, making it difficult to determine whether successful differentiation reflects stable biology or exploitable idiosyncrasies. We introduce a participant-agnostic autoencoder framework that derives profiles from brief resting-state magnetoencephalography (MEG) segments using reconstruction as sole training objective. Discriminative profiles emerged from the learned latent space without participant labels. Within-session, autoencoder profiles reached 93.3% accuracy at 120 s, exceeding functional-connectivity, spectral, and contrastive baselines with recordings as short as 14 s when participant-specific anatomy was withheld from source reconstruction. Differentiation generalized above chance across recording sessions (between-session accuracy 49.5% for the pretrained autoencoder). Profiles also predicted age more accurately than baselines (r^2=0.318), and the decoder enabled perturbation-based sensitivity analyses in spectral and connectivity spaces. This establishes participant-agnostic representation learning as a scalable and interpretable profiling.
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Abstract
Recent neuroimaging research has shown that human brain activity expresses stable, individual-specific features that persist over months to years, defining neurophysiological profiles. Current model-based profiling relies on labeled data and supervised learning, leaving open whether they exploit idiosyncratic artifacts or genuine biology. We introduce a participant-agnostic autoencoder framework to derive differentiable profiles from brief segments of resting-state magnetoencephalography (MEG). Despite an unsupervised objective, discriminative profiles emerged naturally from the learned latent space, outperforming model-free and model-based baselines in participant differentiation. Reliable differentiation was achieved using recordings as short as 14 s, generalized across recording sessions, and remained robust without anatomical information. Beyond differentiation, learned profiles predicted age more accurately than baselines, and the decoder enabled perturbation-based sensitivity analyses directly in spectral and connectivity spaces. These results establish participant-agnostic modeling as a principled and interpretable framework for neurophysiological profiling that generalizes across sessions while preserving sensitivity to biologically relevant individual differences.
Competing Interest Statement
The authors have declared no competing interest.
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