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Lennart P. L. Landsmeer

Publications and source records attributed to Lennart P. L. Landsmeer.

5 recordsLinked to original sources

ADSEQ: A delay-aware autograd-compatible framework for spike-event delivery in SNNs

Spiking neural networks (SNNs), central to computational neuroscience and neuromorphic machine learning (ML), require efficient simulation and gradient-based training. While AI accelerators offer promising speedups, gradient-based SNNs typically implement sparse spike events using dense, memory-heavy data-structures. Existing exact gradient methods lack generality, and current simulators often omit or inefficiently handle delayed spikes. We address this by deriving gradient computation through spike event queues, including delays, and implementing this into memory-efficient, autodifferentiable spike event queues (ADSEQ). These are benchmarked across CPU, GPU, TPU, and LPU platforms. We find that queue design strongly shapes performance. CPUs, as expected, perform well with traditional tree-based or FIFO implementations, while GPUs excel with ring buffers for smaller simulations, yet under higher memory pressure prefer more sparse data-structures. TPUs seem to favor an implementation based on sorting intrinsics. Selective spike dropping provides a simple performance-accuracy trade-off, which could be enhanced by future autograd frameworks adapting diverging primal/tangent data-structures.

cs.NE↗

Gradient Diffusion: Sensitivity-Matrix Co-Simulation Enables Activity Adaptation and Learnable Plasticity in Neural Simulators

Computational neuroscience relies on large-scale dynamical-systems models of neurons, with a vast amount of offline, pre-simulation, tuned parameters, with models often tied to their brain simulators. These fixed parameters lead to stiff models, that show unnatural behaviour when introduced to new environments, or when combined into larger networks. In contrast to offline tuning, in biology, cells continuously adapt via homeostatic plasticity to stay in desired dynamical regimes. In this work, we aim to introduce such online tuning of cellular parameters into brain simulation. We show that the sensitivity equation of a biorealistic neural models has the same shape as a general neuron model, and can be simulated within existing brain simulators. Via co-simulation with the sensitivity equation, we enable both offline, and online tuning of activity of arbitrary biophysically realistic brain models. Furthermore, we show that this opens the possibility to study the biological mechanisms underlying homeostatic plasticity, via both meta-learning plasticity mechanism as well as treating online tuning as a black-box plasticity mechanism. Through the generality of our methods, we hope that more computational science fields can capitalize on the similarity between the simulated model and its gradient system.

q-bio.NC↗

Spatial Spiking Neural Networks Enable Efficient and Robust Temporal Computation

The efficiency of modern machine intelligence depends on high accuracy with minimal computational cost. In spiking neural networks (SNNs), synaptic delays are crucial for encoding temporal structure, yet existing models treat them as fully trainable, unconstrained parameters, leading to large memory footprints, higher computational demand, and a departure from biological plausibility. In the brain, however, delays arise from physical distances between neurons embedded in space. Building on this principle, we introduce Spatial Spiking Neural Networks (SpSNNs), a framework in which neurons learn coordinates in a finite-dimensional Euclidean space and delays emerge from inter-neuron distances. This replaces per-synapse delay learning with position learning, substantially reducing parameter count while retaining temporal expressiveness. Across the Yin-Yang and Spiking Heidelberg Digits benchmarks, SpSNNs outperform SNNs with unconstrained delays despite using far fewer parameters. Performance consistently peaks in 2D and 3D networks rather than infinite-dimensional delay spaces, revealing a geometric regularization effect. Moreover, dynamically sparsified SpSNNs maintain full accuracy even at 90% sparsity, matching standard delay-trained SNNs while using up to 18x fewer parameters. Because learned spatial layouts map naturally onto hardware geometries, SpSNNs lend themselves to efficient neuromorphic implementation. Methodologically, SpSNNs compute exact delay gradients via automatic differentiation with custom-derived rules, supporting arbitrary neuron models and architectures. Altogether, SpSNNs provide a principled platform for exploring spatial structure in temporal computation and offer a hardware-friendly substrate for scalable, energy-efficient neuromorphic intelligence.

cs.NE↗

A Lightweight Architecture for Real-Time Neuronal-Spike Classification

Electrophysiological recordings of neural activity in a mouse's brain are very popular among neuroscientists for understanding brain function. One particular area of interest is acquiring recordings from the Purkinje cells in the cerebellum in order to understand brain injuries and the loss of motor functions. However, current setups for such experiments do not allow the mouse to move freely and, thus, do not capture its natural behaviour since they have a wired connection between the animal's head stage and an acquisition device. In this work, we propose a lightweight neuronal-spike detection and classification architecture that leverages on the unique characteristics of the Purkinje cells to discard unneeded information from the sparse neural data in real time. This allows the (condensed) data to be easily stored on a removable storage device on the head stage, alleviating the need for wires. Synthesis results reveal a >95% overall classification accuracy while still resulting in a small-form-factor design, which allows for the free movement of mice during experiments. Moreover, the power-efficient nature of the design and the usage of STT-RAM (Spin Transfer Torque Magnetic Random Access Memory) as the removable storage allows the head stage to easily operate on a tiny battery for up to approximately 4 days.

cs.AR↗

Tricking AI chips into Simulating the Human Brain: A Detailed Performance Analysis

Challenging the Nvidia monopoly, dedicated AI-accelerator chips have begun emerging for tackling the computational challenge that the inference and, especially, the training of modern deep neural networks (DNNs) poses to modern computers. The field has been ridden with studies assessing the performance of these contestants across various DNN model types. However, AI-experts are aware of the limitations of current DNNs and have been working towards the fourth AI wave which will, arguably, rely on more biologically inspired models, predominantly on spiking neural networks (SNNs). At the same time, GPUs have been heavily used for simulating such models in the field of computational neuroscience, yet AI-chips have not been tested on such workloads. The current paper aims at filling this important gap by evaluating multiple, cutting-edge AI-chips (Graphcore IPU, GroqChip, Nvidia GPU with Tensor Cores and Google TPU) on simulating a highly biologically detailed model of a brain region, the inferior olive (IO). This IO application stress-tests the different AI-platforms for highlighting architectural tradeoffs by varying its compute density, memory requirements and floating-point numerical accuracy. Our performance analysis reveals that the simulation problem maps extremely well onto the GPU and TPU architectures, which for networks of 125,000 cells leads to a 28x respectively 1,208x speedup over CPU runtimes. At this speed, the TPU sets a new record for largest real-time IO simulation. The GroqChip outperforms both platforms for small networks but, due to implementing some floating-point operations at reduced accuracy, is found not yet usable for brain simulation.

cs.LG↗