Artificial Neural Networks (ANNs) are bio-inspired models of neural computation that have proven highly effective. Still, ANNs lack a natural notion of time, and neural units in ANNs exchange analog values in a frame-based manner, a computationally and energetically inefficient form of communication. This contrasts sharply with biological neurons that communicate sparingly and efficiently using isomorphic binary spikes. While Spiking Neural Networks (SNNs) can be constructed by replacing the units of an ANN with spiking neurons (Cao et al., 2015; Diehl et al., 2015) to obtain reasonable performance, these SNNs use Poisson spiking mechanisms with exceedingly high firing rates compared to their biological counterparts. Here we show how spiking neurons that employ a form of neural coding can be used to construct SNNs that match high-performance ANNs and match or exceed state-of-the-art in SNNs on important benchmarks, while requiring firing rates compatible with biological findings. For this, we use spike-based coding based on the firing rate limiting adaptation phenomenon observed in biological spiking neurons. This phenomenon can be captured in fast adapting spiking neuron models, for which we derive the effective transfer function. Neural units in ANNs trained with this transfer function can be substituted directly with adaptive spiking neurons, and the resulting Adaptive SNNs (AdSNNs) can carry out competitive classification in deep neural networks without further modifications. Adaptive spike-based coding additionally allows for the dynamic control of neural coding precision: we show empirically how a simple model of arousal in AdSNNs further halves the average required firing rate and this notion naturally extends to other forms of attention as studied in neuroscience. AdSNNs thus hold promise as a novel and sparsely active model for neural computation that naturally fits to temporally continuous and asynchronous applications.

The folding structure of the DNA molecule combined with helper molecules, also referred to as the chromatin, is highly relevant for the functional properties of DNA. The chromatin structure is largely determined by the underlying primary DNA sequence, though the interaction is not yet fully understood. In this paper we develop a convolutional neural network that takes an image-representation of primary DNA sequence as its input, and predicts key determinants of chromatin structure. The method is developed such that it is capable of detecting interactions between distal elements in the DNA sequence, which are known to be highly relevant. Our experiments show that the method outperforms several existing methods both in terms of prediction accuracy and training time.

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As living organisms, one of our primary characteristics is the ability to rapidly process and react to unknown and unexpected events. To this end, we are able to recognize an event or a sequence of events and learn to respond properly. Despite advances in machine learning, current cognitive robotic systems are not able to rapidly and efficiently respond in the real world: the challenge is to learn to recognize both what is important, and also when to act. Reinforcement Learning (RL) is typically used to solve complex tasks: to learn the how. To respond quickly-to learn when-the environment has to be sampled often enough. For "enough", a programmer has to decide on the step-size as a timerepresentation, choosing between a fine-grained representation of time (many state-transitions; difficult to learn with RL) or to a coarse temporal resolution (easier to learn with RL but lacking precise timing). Here, we derive a continuous-time version of on-policy SARSA-learning in a working-memory neural network model, AuGMEnT. Using a neural working memory network resolves the what problem, our when solution is built on the notion that in the real world, instantaneous actions of duration dt are actually impossible. We demonstrate how we can decouple action duration from the internal time-steps in the neural RL model using an action selection system. The resultant CT-AuGMEnT successfully learns to react to the events of a continuous-time task, without any pre-imposed specifications about the duration of the events or the delays between them.

Spatial attention enhances sensory processing of goal-relevant information and improves perceptual sensitivity. Yet, the specific neural mechanisms underlying the effects of spatial attention on performance are still contested. Here, we examine different attention mechanisms in spiking deep convolutional neural networks. We directly contrast effects of precision (internal noise suppression) and two different gain modulation mechanisms on performance on a visual search task with complex real-world images. Unlike standard artificial neurons, biological neurons have saturating activation functions, permitting implementation of attentional gain as gain on a neuron's input or on its outgoing connection. We show that modulating the connection is most effective in selectively enhancing information processing by redistributing spiking activity and by introducing additional task-relevant information, as shown by representational similarity analyses. Precision only produced minor attentional effects in performance. Our results, which mirror empirical findings, show that it is possible to adjudicate between attention mechanisms using more biologically realistic models and natural stimuli.