VLDB 2026 Research / reviewers in the wild / expert
Espen Hagen
dblp:13/3780
· DBLP profile ↗
5ranked-venue papers
2as first author
1since 2021 · last 2022
0000-0002-1321-5970ORCID · corroborated
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 3 · 1 first-author · 1 since 2021Artificial intelligence and machine learning · 2 · 1 first-authorGraphics, computer vision, multimedia, augmented reality and games · 1 · 1 first-author
Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.
| Artificial intelligence
1 paper |
Probabilistic and Bayesian machine learning · 100% | |
| Interdisciplinary, comprehensive, and emerging computing
1 paper |
Bioinformatics and computational biology · 100% | |
| Computer architecture, parallel and distributed computing, and storage systems
1 paper |
Hardware accelerators and domain-specific architectures · 100% |
Topics — the 5 heaviest of 5, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Machine learning › Probabilistic and Bayesian machine learning › statistical inference › bayesian inference
bayesian nonparametric model |
0.3 | 1 | 2017 | YASS: Yet Another Spike Sorter · NIPS 2017 |
Machine learning › Probabilistic and Bayesian machine learning › statistical inference › bayesian inference › bayesian nonparametric model
dirichlet process mixture model |
0.3 | 1 | 2017 | YASS: Yet Another Spike Sorter · NIPS 2017 |
Bioinformatics and computational biology
computational neuroscience |
0.3 | 1 | 2017 | YASS: Yet Another Spike Sorter · NIPS 2017 |
Bioinformatics and computational biology › neuroscience › neuroinformatics › neural data analysis
spike sorting |
0.3 | 1 | 2017 | YASS: Yet Another Spike Sorter · NIPS 2017 |
Hardware accelerators and domain-specific architectures › machine learning accelerator
neural network accelerator |
0.1 | 1 | 2017 | YASS: Yet Another Spike Sorter · NIPS 2017 |
Methods — techniques the papers use, named apart from their topics
neural network detection · 0.9matching pursuit deconvolution · 0.9coreset · 0.9
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2022 | Brain signal predictions from multi-scale networks using a linearized frameworkabstractSimulations of neural activity at different levels of detail are ubiquitous in modern neurosciences, aiding the interpretation of experimental data and underlying neural mechanisms at the level of cells and circuits. Extracellular measurements of brain signals reflecting transmembrane currents throughout the neural tissue remain commonplace. The lower frequencies (≲ 300Hz) of measured signals generally stem from synaptic activity driven by recurrent interactions among neural populations and computational models should also incorporate accurate predictions of such signals. Due to limited computational resources, large-scale neuronal network models (≳ 106 neurons or so) often require reducing the level of biophysical detail and account mainly for times of action potentials ('spikes') or spike rates. Corresponding extracellular signal predictions have thus poorly accounted for their biophysical origin. Here we propose a computational framework for predicting spatiotemporal filter kernels for such extracellular signals stemming from synaptic activity, accounting for the biophysics of neurons, populations, and recurrent connections. Signals are obtained by convolving population spike rates by appropriate kernels for each connection pathway and summing the contributions. Our main results are that kernels derived via linearized synapse and membrane dynamics, distributions of cells, conduction delay, and volume conductor model allow for accurately capturing the spatiotemporal dynamics of ground truth extracellular signals from conductance-based multicompartment neuron networks. One particular observation is that changes in the effective membrane time constants caused by persistent synapse activation must be accounted for. The work also constitutes a major advance in computational efficiency of accurate, biophysics-based signal predictions from large-scale spike and rate-based neuron network models drastically reducing signal prediction times compared to biophysically detailed network models. This work also provides insight into how experimentally recorded low-frequency extracellular signals of neuronal activity may be approximately linearly dependent on spiking activity. A new software tool LFPykernels serves as a reference implementation of the framework. Espen Hagen, Steinn H. Magnusson, Torbjørn V. Ness, Geir Halnes, Pooja N. Babu, Charl A. P. Linssen, Abigail Morrison, Gaute T. Einevoll |
PLoS Comput. Biol. | 1 |
| 2020 | Estimation of neural network model parameters from local field potentials (LFPs)abstractMost modeling in systems neuroscience has been descriptive where neural representations such as 'receptive fields', have been found by statistically correlating neural activity to sensory input. In the traditional physics approach to modelling, hypotheses are represented by mechanistic models based on the underlying building blocks of the system, and candidate models are validated by comparing with experiments. Until now validation of mechanistic cortical network models has been based on comparison with neuronal spikes, found from the high-frequency part of extracellular electrical potentials. In this computational study we investigated to what extent the low-frequency part of the signal, the local field potential (LFP), can be used to validate and infer properties of mechanistic cortical network models. In particular, we asked the question whether the LFP can be used to accurately estimate synaptic connection weights in the underlying network. We considered the thoroughly analysed Brunel network comprising an excitatory and an inhibitory population of recurrently connected integrate-and-fire (LIF) neurons. This model exhibits a high diversity of spiking network dynamics depending on the values of only three network parameters. The LFP generated by the network was computed using a hybrid scheme where spikes computed from the point-neuron network were replayed on biophysically detailed multicompartmental neurons. We assessed how accurately the three model parameters could be estimated from power spectra of stationary 'background' LFP signals by application of convolutional neural nets (CNNs). All network parameters could be very accurately estimated, suggesting that LFPs indeed can be used for network model validation. Jan-Eirik W. Skaar, Alexander J. Stasik, Espen Hagen, Torbjørn V. Ness, Gaute T. Einevoll |
PLoS Comput. Biol. | 3 |
| 2017 | YASS: Yet Another Spike SorterabstractSpike sorting is a critical first step in extracting neural signals from large-scale electrophysiological data. This manuscript describes an efficient, reliable pipeline for spike sorting on dense multi-electrode arrays (MEAs), where neural signals appear across many electrodes and spike sorting currently represents a major computational bottleneck. We present several new techniques that make dense MEA spike sorting more robust and scalable. Our pipeline is based on an efficient multi-stage ''triage-then-cluster-then-pursuit'' approach that initially extracts only clean, high-quality waveforms from the electrophysiological time series by temporarily skipping noisy or ''collided'' events (representing two neurons firing synchronously). This is accomplished by developing a neural network detection method followed by efficient outlier triaging. The clean waveforms are then used to infer the set of neural spike waveform templates through nonparametric Bayesian clustering. Our clustering approach adapts a ''coreset'' approach for data reduction and uses efficient inference methods in a Dirichlet process mixture model framework to dramatically improve the scalability and reliability of the entire pipeline. The ''triaged'' waveforms are then finally recovered with matching-pursuit deconvolution techniques. The proposed methods improve on the state-of-the-art in terms of accuracy and stability on both real and biophysically-realistic simulated MEA data. Furthermore, the proposed pipeline is efficient, learning templates and clustering faster than real-time for a 500-electrode dataset, largely on a single CPU core. Jin Hyung Lee, David E. Carlson, Hooshmand Shokri Razaghi, Weichi Yao, Georges Goetz, Espen Hagen, Eleanor Batty, E. J. Chichilnisky, Gaute T. Einevoll, Liam Paninski |
NIPS | 6 |
| 2016 | Biophysical Network Modelling of the dLGN Circuit: Different Effects of Triadic and Axonal Inhibition on Visual Responses of Relay CellsabstractDespite its prominent placement between the retina and primary visual cortex in the early visual pathway, the role of the dorsal lateral geniculate nucleus (dLGN) in molding and regulating the visual signals entering the brain is still poorly understood. A striking feature of the dLGN circuit is that relay cells (RCs) and interneurons (INs) form so-called triadic synapses, where an IN dendritic terminal can be simultaneously postsynaptic to a retinal ganglion cell (GC) input and presynaptic to an RC dendrite, allowing for so-called triadic inhibition. Taking advantage of a recently developed biophysically detailed multicompartmental model for an IN, we here investigate putative effects of these different inhibitory actions of INs, i.e., triadic inhibition and standard axonal inhibition, on the response properties of RCs. We compute and investigate so-called area-response curves, that is, trial-averaged visual spike responses vs. spot size, for circular flashing spots in a network of RCs and INs. The model parameters are grossly tuned to give results in qualitative accordance with previous in vivo data of responses to such stimuli for cat GCs and RCs. We particularly investigate how the model ingredients affect salient response properties such as the receptive-field center size of RCs and INs, maximal responses and center-surround antagonisms. For example, while triadic inhibition not involving firing of IN action potentials was found to provide only a non-linear gain control of the conversion of input spikes to output spikes by RCs, axonal inhibition was in contrast found to substantially affect the receptive-field center size: the larger the inhibition, the more the RC center size shrinks compared to the GC providing the feedforward excitation. Thus, a possible role of the different inhibitory actions from INs to RCs in the dLGN circuit is to provide separate mechanisms for overall gain control (direct triadic inhibition) and regulation of spatial resolution (axonal inhibition) of visual signals sent to cortex. Thomas Heiberg, Espen Hagen, Geir Halnes, Gaute T. Einevoll |
PLoS Comput. Biol. | 2 |
| 1992 | Navigation by optical flowabstractA new navigation method based on measurements of image token positions and Kalman filtering is presented. An image token is the central projection of a landmark, a point on the terrain surface. This surface being described by a topographical map, the Kalman filter processes the measurements to update estimates of camera position and orientation, and landmark positions. Tests of an implementation for aeroplane navigation indicate a performance comparable to, or better than, that of satellite navigation systems. The implemented algorithm also seems to have a high tolerance against noise and modelling errors.> Espen Hagen, Eilert Heyerdahl |
ICPR (1) | 1 |