Deep Convolutional Neural Networks (CNNs) have recently demonstrated impressive results in electroencephalogram (EEG) decoding for several Brain-Computer Interface (BCI) paradigms, including Motor-Imagery (MI). However, neurophysiological processes underpinning EEG signals vary across subjects causing covariate shifts in data distributions and hence hindering the generalization of deep models across subjects. In this paper, we aim to address the challenge of inter-subject variability in MI. To this end, we employ causal reasoning to characterize all possible distribution shifts in the MI task and propose a dynamic convolution framework to account for shifts caused by the inter-subject variability. Using publicly available MI datasets, we demonstrate improved generalization performance (up to 5%) across subjects in various MI tasks for four well-established deep architectures.

Understanding the development and differentiation of the neocortex remains a central focus of neuroscience. While previous studies have examined isolated aspects of cellular and synaptic organization, an integrated functional index of the cortical microcircuit is still lacking. Here we aimed to provide such an index, in the form of spontaneously recurring periods of persistent network activity -or Up states- recorded in mouse cortical slices. These coordinated network dynamics emerge through the orchestrated regulation of multiple cellular and synaptic elements and represent the default activity of the cortical microcircuit. To explore whether spontaneous Up states can capture developmental changes in intracortical networks we obtained local field potential recordings throughout the mouse lifespan. Two independent and complementary methodologies revealed that Up state activity is systematically modified by age, with the largest changes occurring during early development and adolescence. To explore possible regional heterogeneities we also compared the development of Up states in two distinct cortical areas and show that primary somatosensory cortex develops at a faster pace than primary motor cortex. Our findings suggest that in vitro Up states can serve as a functional index of cortical development and differentiation and can provide a baseline for comparing experimental and/or genetic mouse models.