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Dragoi, T.

Publications and source records attributed to Dragoi, T..

2 recordsLinked to original sources

BiXformer: A Bidirectional Cross Attention Transformer for Disentangling Inter-Regional Neural Dynamics

Advances in high-throughput neural recording technologies enable simultaneous measurement of activity across multiple brain regions in behaving animals, producing datasets of unprecedented scale and richness. Interpreting these data remains challenging due to the bidirectional and temporally offset nature of inter-regional communication, where feedforward and feedback signals are superimposed within neural populations. We introduce BiXformer, a bidirectional cross-attention transformer that disentangles these interactions by decomposing inter-regional communication into causal and acausal streams using directionally masked attention. By enforcing temporal constraints within attention heads, BiXformer recovers low-dimensional, directed latent dynamics and estimates communication delays without relying on linearity or stationarity assumptions. We validate the model on synthetic datasets with known ground-truth delays, demonstrating accurate recovery of both latent structure and inter-regional timing. Applied to simultaneous neural-behavioral recordings and multi-region neural recordings during a movement task, BiXformer reveals interpretable, temporally structured components consistent with the coexistence of sensory feedback and motor-related signals. These results establish BiXformer as a flexible framework for uncovering dynamic, directed communication in complex neural circuits.

neuroscience↗

Dynamic engagement of the motor cortex in controlling movement

Neural circuits do not contribute equally or continuously to behavior. In mice, the motor cortex can be essential or dispensable for movement in different contexts, but how it is dynamically recruited as behavioral demands evolve remains unclear. Here, we demonstrate that motor cortical involvement in movement exhibits rapid, discrete state transitions even during movements that otherwise appear continuous. While robust and reproducible across animals, the timing and presence of these state transitions are highly sensitive to task structure. We find that motor cortical engagement is sustained under conditions of sensorimotor uncertainty and dissipates rapidly when sensorimotor contingencies are resolved and actions and outcomes thus become predictable. These findings reveal a previously unrecognized layer of fast-timescale flexibility in the neural control of movement and offer a conceptual framework for understanding how cortical circuits dynamically govern behavior as demands evolve.

neuroscience↗