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In this work we develop a model of predictive learning on neuromorphic hardware. Our model uses the on-chip plasticity capabilities of the Loihi chip to remember observed sequences of events and use this memory to generate predictions of future events in real time. Given the locality constraints of on-chip plasticity rules, generating predictions without interfering with the ongoing learning process is nontrivial. We address this challenge with a memory consolidation approach inspired by hippocampal replay. Sequence memory is stored in an initial memory module using spike-timing dependent plasticity. Later, during an offline period, memories are consolidated into a distinct prediction module. This second module is then able to represent predicted future events without interfering with the activity, and plasticity, in the first module, enabling online comparison between predictions and ground-truth observations. Our model serves as a proof-of-concept that online predictive learning models can be deployed on neuromorphic hardware with on-chip plasticity., Comment: NICE 2022

Interest in biologically inspired alternatives to backpropagation is driven by the desire to both advance connections between deep learning and neuroscience and address backpropagation's shortcomings on tasks such as online, continual learning. However, local synaptic learning rules like those employed by the brain have so far failed to match the performance of backpropagation in deep networks. In this study, we employ meta-learning to discover networks that learn using feedback connections and local, biologically inspired learning rules. Importantly, the feedback connections are not tied to the feedforward weights, avoiding biologically implausible weight transport. Our experiments show that meta-trained networks effectively use feedback connections to perform online credit assignment in multi-layer architectures. Surprisingly, this approach matches or exceeds a state-of-the-art gradient-based online meta-learning algorithm on regression and classification tasks, excelling in particular at continual learning. Analysis of the weight updates employed by these models reveals that they differ qualitatively from gradient descent in a way that reduces interference between updates. Our results suggest the existence of a class of biologically plausible learning mechanisms that not only match gradient descent-based learning, but also overcome its limitations.

Recurrent neural networks with differentiable attention mechanisms have had success in generative and classification tasks. We show that the classification performance of such models can be enhanced by guiding a randomly initialized model to attend to salient regions of the input in early training iterations. We further show that, if explicit heuristics for guidance are unavailable, a model that is pretrained on an unsupervised reconstruction task can discover good attention policies without supervision. We demonstrate that increased efficiency of the attention mechanism itself contributes to these performance improvements. Based on these insights, we introduce bootstrapped glimpse mimicking, a simple, theoretically task-general method of more effectively training attention models. Our work draws inspiration from and parallels results on human learning of attention., Comment: Presented at NIPS 2017 Workshop on Cognitively Informed Artificial Intelligence

Making inferences about the computations performed by neuronal circuits from synapse-level connectivity maps is an emerging opportunity in neuroscience. The mushroom body (MB) is well positioned for developing and testing such an approach due to its conserved neuronal architecture, recently completed dense connectome, and extensive prior experimental studies of its roles in learning, memory, and activity regulation. Here, we identify new components of the MB circuit inDrosophila, including extensive visual input and MB output neurons (MBONs) with direct connections to descending neurons. We find unexpected structure in sensory inputs, in the transfer of information about different sensory modalities to MBONs, and in the modulation of that transfer by dopaminergic neurons (DANs). We provide insights into the circuitry used to integrate MB outputs, connectivity between the MB and the central complex and inputs to DANs, including feedback from MBONs. Our results provide a foundation for further theoretical and experimental work.