An Instruction Language for Self-Construction in the Context of Neural Networks

Biological systems are based on an entirely different concept of construction than human artifacts. They construct themselves by a process of self-organization that is a systematic spatio-temporal generation of, and interaction between, various specialized cell types. We propose a framework for designing gene-like codes for guiding the self-construction of neural networks. The description of neural development is formalized by defining a set of primitive actions taken locally by neural precursors during corticogenesis. These primitives can be combined into networks of instructions similar to biochemical pathways, capable of reproducing complex developmental sequences in a biologically plausible way. Moreover, the conditional activation and deactivation of these instruction networks can also be controlled by these primitives, allowing for the design of a “genetic code” containing both coding and regulating elements. We demonstrate in a simulation of physical cell development how this code can be incorporated into a single progenitor, which then by replication and differentiation, reproduces important aspects of corticogenesis

DYNAP-SE2: a scalable multi-core dynamic neuromorphic asynchronous spiking neural network processor

With the remarkable progress that technology has made, the need for processing data near the sensors at the edge has increased dramatically. The electronic systems used in these applications must process data continuously, in real-time, and extract relevant information using the smallest possible energy budgets. A promising approach for implementing always-on processing of sensory signals that supports on-demand, sparse, and edge-computing is to take inspiration from biological nervous system. Following this approach, we present a brain-inspired platform for prototyping real-time event-based Spiking Neural Networks (SNNs). The system proposed supports the direct emulation of dynamic and realistic neural processing phenomena such as short-term plasticity, NMDA gating, AMPA diffusion, homeostasis, spike frequency adaptation, conductance-based dendritic compartments and spike transmission delays. The analog circuits that implement such primitives are paired with a low latency asynchronous digital circuits for routing and mapping events. This asynchronous infrastructure enables the definition of different network architectures, and provides direct event-based interfaces to convert and encode data from event-based and continuous-signal sensors. Here we describe the overall system architecture, we characterize the mixed signal analog-digital circuits that emulate neural dynamics, demonstrate their features with experimental measurements, and present a low- and high-level software ecosystem that can be used for configuring the system. The flexibility to emulate different biologically plausible neural networks, and the chip's ability to monitor both population and single neuron signals in real-time, allow to develop and validate complex models of neural processing for both basic research and edge-computing applications

DYNAP-SE2: a scalable multi-core dynamic neuromorphic asynchronous spiking neural network processor

With the remarkable progress that technology has made, the need for processing data near the sensors at the edge has increased dramatically. The electronic systems used in these applications must process data continuously, in real-time, and extract relevant information using the smallest possible energy budgets. A promising approach for implementing always-on processing of sensory signals that supports on-demand, sparse, and edge-computing is to take inspiration from biological nervous system. Following this approach, we present a brain-inspired platform for prototyping real-time event-based Spiking Neural Networks (SNNs). The system proposed supports the direct emulation of dynamic and realistic neural processing phenomena such as short-term plasticity, NMDA gating, AMPA diffusion, homeostasis, spike frequency adaptation, conductance-based dendritic compartments and spike transmission delays. The analog circuits that implement such primitives are paired with a low latency asynchronous digital circuits for routing and mapping events. This asynchronous infrastructure enables the definition of different network architectures, and provides direct event-based interfaces to convert and encode data from event-based and continuous-signal sensors. Here we describe the overall system architecture, we characterize the mixed signal analog-digital circuits that emulate neural dynamics, demonstrate their features with experimental measurements, and present a low- and high-level software ecosystem that can be used for configuring the system. The flexibility to emulate different biologically plausible neural networks, and the chip's ability to monitor both population and single neuron signals in real-time, allow to develop and validate complex models of neural processing for both basic research and edge-computing applications

International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways.

Primary biliary cirrhosis (PBC) is a classical autoimmune liver disease for which effective immunomodulatory therapy is lacking. Here we perform meta-analyses of discovery data sets from genome-wide association studies of European subjects (n=2,764 cases and 10,475 controls) followed by validation genotyping in an independent cohort (n=3,716 cases and 4,261 controls). We discover and validate six previously unknown risk loci for PBC (Pcombined<5 × 10(-8)) and used pathway analysis to identify JAK-STAT/IL12/IL27 signalling and cytokine-cytokine pathways, for which relevant therapies exist