NEST 3.9 is the result of 1217 commits by 24 developers since NEST 3.8 which was released on 2024-08-02. This release notably adds features for several models, specifically, biologically-inspired f...

While the implementation of learning and memory in the brain is governed in large part by subcellular mechanims in the dendrites of neurons, large-scale network simulations featuring such processes remain challenging to achieve. This can be attributed to a lack of appropriate software tools, as neuroscientific simulation software focuses on the one hand on highly detailed models, and on the other hand on massive networks featuring point-neurons. Here, we fill this gap by implementing a framework for the massively parallel simulation of simplified dendrite models with customizable subcellular dynamics. To achieve this, we leverage the NEural Simulation Tool (NEST), the neuroscientific reference with respect to efficient massively parallel simulations of point neuron networks. By co-opting the already existing model descriptions language NESTML, we generate C++ code implementing user-configurable subcellular dynamics. Through benchmarking and profiling, we show that the generated models run efficiently, leading to scalable NEST network simulations. We demonstrate relevant functionalities by showing that a key sensory computation – the association of top-down context arriving at distal dendrites in layer 1 and feedforward sensory input arriving perisomatically – can be achieved in a single shot fashion through apical calcium dynamics. Our work thus unlocks the study of how dendritic processes shape learning, and in particular of how brain-wide communication through long-range, layer 1-targetting connections steers perisomatic plasticity. ### Competing Interest Statement The authors have declared no competing interest. Helmholtz Association of German Research Centres, https://ror.org/0281dp749 Italian Ministry for Universities and Research (MUR), CUP I53C22001400006, CUP B51E22000150006

While simulating compartmental dynamics in response to various input patterns is the prevalent technique for understanding dendritic computation, a great deal can be learned from classical analytical methods that provide solutions for the dendritic voltage. For example, such solutions are needed to simplify spatially extended neuron models, to understand frequency-dependent response properties, to elucidate the interaction between synaptic inputs, and hence to reveal the effective compartmentalization of dendrites into functional subunits. Nevertheless, these methods have not been implemented in modern software tools. This works describes the NEural Analysis Toolkit (NEAT), a Python toolbox that implements classical algorithms to compute response properties of spatially extended neuron models, and that leverages these algorithms to simplify them. Packaged with this are a range of useful utilities to plot morphologies and spatial quantities defined on the morphology, to distribute locations on the morphology, and to select parts of the morphology to e.g. apply morphological ablations or alter the membrane properties. The resulting models can be exported to NEURON and NEST, two commonly used simulators, the former focused on detailed single neuron model simulations, and the latter geared towards distributed network simulations. As a consequence, this toolbox provides a missing link between single neuron computation and large-scale network analysis, substantially facilitating the study of the role of dendritic computation in shaping emergent network dynamics. NEAT is available through pip under the name ‘nest-neat’, or from its source code (<https://github.com/nest/NEAT>), which is provided under the GNU General Public License. Furthermore, support for NEAT is provided on its GitHub page and through the NEST user mailing list (users{at}nest-simulator.org). ### Competing Interest Statement The authors have declared no competing interest. Helmholtz Association of German Research Centres, https://ror.org/0281dp749

spiking neural networks simulations with energy-dependent neuron and synapse models - Wiss/edsnn