Demo Data from EDBT 2026 / reviewers in the wild / expert
Emmanouil Froudarakis
dblp:161/4141
· DBLP profile ↗
5ranked-venue papers
0as first author
0since 2021 · last 2020
0000-0002-3249-3845ORCID · corroborated
Domains — the database's venue-derived domains; a paper can count in several
Artificial intelligence and machine learning · 3Applied, interdisciplinary, general and emerging computing · 2
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.
| Interdisciplinary, comprehensive, and emerging computing
3 papers |
Bioinformatics and computational biology · 100% | |
| Artificial intelligence
3 papers |
Deep learning architectures and training · 66% 3D vision · 34% | |
| Databases, data mining, and information retrieval
1 paper |
Data mining · 100% |
Topics — the 11 heaviest of 11, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology
computational neuroscience |
0.4 | 2 | 2019 | Stimulus domain transfer in recurrent models for large scale cortical population prediction on video · NeurIPS 2018 A rotation-equivariant convolutional neural network model of primary visual cortex · ICLR (Poster) 2019 |
Computer vision › 3D vision › local feature descriptor
rotation-invariant descriptor |
0.4 | 1 | 2020 | Rotation-invariant clustering of neuronal responses in primary visual cortex · ICLR 2020 |
Data mining
clustering |
0.4 | 1 | 2020 | Rotation-invariant clustering of neuronal responses in primary visual cortex · ICLR 2020 |
Machine learning › Deep learning architectures and training
convolutional neural network |
0.4 | 1 | 2019 | A rotation-equivariant convolutional neural network model of primary visual cortex · ICLR (Poster) 2019 |
Machine learning › Deep learning architectures and training
equivariant neural network |
0.4 | 1 | 2019 | A rotation-equivariant convolutional neural network model of primary visual cortex · ICLR (Poster) 2019 |
Bioinformatics and computational biology › computational neuroscience › neural response modeling
neural response prediction |
0.3 | 1 | 2018 | Stimulus domain transfer in recurrent models for large scale cortical population prediction on video · NeurIPS 2018 |
Bioinformatics and computational biology › computational neuroscience › neural coding
sensory coding |
0.3 | 1 | 2018 | Stimulus domain transfer in recurrent models for large scale cortical population prediction on video · NeurIPS 2018 |
Bioinformatics and computational biology › computational neuroscience
visual cortex |
0.3 | 1 | 2018 | Stimulus domain transfer in recurrent models for large scale cortical population prediction on video · NeurIPS 2018 |
Bioinformatics and computational biology
neuroscience |
0.1 | 1 | 2020 | Rotation-invariant clustering of neuronal responses in primary visual cortex · ICLR 2020 |
Bioinformatics and computational biology › computational neuroscience › visual cortex
visual cortex modeling |
0.1 | 1 | 2019 | A rotation-equivariant convolutional neural network model of primary visual cortex · ICLR (Poster) 2019 |
Machine learning › Deep learning architectures and training
recurrent neural network |
0.1 | 1 | 2018 | Stimulus domain transfer in recurrent models for large scale cortical population prediction on video · NeurIPS 2018 |
Methods — techniques the papers use, named apart from their topics
rotation-invariant clustering · 1.3two-photon microscopy · 0.7recurrent neural network · 0.7fine-tuning · 0.7domain transfer · 0.7
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2020 | Rotation-invariant clustering of neuronal responses in primary visual cortex
Ivan Ustyuzhaninov, Santiago A. Cadena, Emmanouil Froudarakis, Paul G. Fahey, Edgar Y. Walker, Erick Cobos, Jacob Reimer, Fabian H. Sinz, Andreas S. Tolias, Matthias Bethge, Alexander S. Ecker |
ICLR | 3 |
| 2019 | A rotation-equivariant convolutional neural network model of primary visual cortex
Alexander S. Ecker, Fabian H. Sinz, Emmanouil Froudarakis, Paul G. Fahey, Santiago A. Cadena, Edgar Y. Walker, Erick Cobos, Jacob Reimer, Andreas S. Tolias, Matthias Bethge |
ICLR (Poster) | 3 |
| 2018 | Stimulus domain transfer in recurrent models for large scale cortical population prediction on videoabstractTo better understand the representations in visual cortex, we need to generate better predictions of neural activity in awake animals presented with their ecological input: natural video. Despite recent advances in models for static images, models for predicting responses to natural video are scarce and standard linear-nonlinear models perform poorly. We developed a new deep recurrent network architecture that predicts inferred spiking activity of thousands of mouse V1 neurons simultaneously recorded with two-photon microscopy, while accounting for confounding factors such as the animal's gaze position and brain state changes related to running state and pupil dilation. Powerful system identification models provide an opportunity to gain insight into cortical functions through in silico experiments that can subsequently be tested in the brain. However, in many cases this approach requires that the model is able to generalize to stimulus statistics that it was not trained on, such as band-limited noise and other parameterized stimuli. We investigated these domain transfer properties in our model and find that our model trained on natural images is able to correctly predict the orientation tuning of neurons in responses to artificial noise stimuli. Finally, we show that we can fully generalize from movies to noise and maintain high predictive performance on both stimulus domains by fine-tuning only the final layer's weights on a network otherwise trained on natural movies. The converse, however, is not true. Fabian H. Sinz, Alexander S. Ecker, Paul G. Fahey, Edgar Y. Walker, Erick Cobos, Emmanouil Froudarakis, Dimitri Yatsenko, Xaq Pitkow, Jacob Reimer, Andreas S. Tolias |
NeurIPS | 6 |
| 2018 | Community-based benchmarking improves spike rate inference from two-photon calcium imaging dataabstractIn recent years, two-photon calcium imaging has become a standard tool to probe the function of neural circuits and to study computations in neuronal populations. However, the acquired signal is only an indirect measurement of neural activity due to the comparatively slow dynamics of fluorescent calcium indicators. Different algorithms for estimating spike rates from noisy calcium measurements have been proposed in the past, but it is an open question how far performance can be improved. Here, we report the results of the spikefinder challenge, launched to catalyze the development of new spike rate inference algorithms through crowd-sourcing. We present ten of the submitted algorithms which show improved performance compared to previously evaluated methods. Interestingly, the top-performing algorithms are based on a wide range of principles from deep neural networks to generative models, yet provide highly correlated estimates of the neural activity. The competition shows that benchmark challenges can drive algorithmic developments in neuroscience. Philipp Berens, Jeremy Freeman, Thomas Deneux, Nicolay Chenkov, Thomas McColgan, Artur Speiser, Jakob H. Macke, Srinivas C. Turaga, Patrick J. Mineault, Peter Rupprecht, Stephan Gerhard, Rainer W. Friedrich, Johannes Friedrich, Liam Paninski, Marius Pachitariu, Kenneth D. Harris, Ben Bolte, Timothy A. Machado, Dario Ringach, Jasmine Stone, Luke E. Rogerson, Nicolas J. Sofroniew, Jacob Reimer, Emmanouil Froudarakis, Thomas Euler, Miroslav Román Rosón, Lucas Theis, Andreas S. Tolias, Matthias Bethge |
PLoS Comput. Biol. | 24 |
| 2015 | Improved Estimation and Interpretation of Correlations in Neural CircuitsabstractAmbitious projects aim to record the activity of ever larger and denser neuronal populations in vivo. Correlations in neural activity measured in such recordings can reveal important aspects of neural circuit organization. However, estimating and interpreting large correlation matrices is statistically challenging. Estimation can be improved by regularization, i.e. by imposing a structure on the estimate. The amount of improvement depends on how closely the assumed structure represents dependencies in the data. Therefore, the selection of the most efficient correlation matrix estimator for a given neural circuit must be determined empirically. Importantly, the identity and structure of the most efficient estimator informs about the types of dominant dependencies governing the system. We sought statistically efficient estimators of neural correlation matrices in recordings from large, dense groups of cortical neurons. Using fast 3D random-access laser scanning microscopy of calcium signals, we recorded the activity of nearly every neuron in volumes 200 μm wide and 100 μm deep (150-350 cells) in mouse visual cortex. We hypothesized that in these densely sampled recordings, the correlation matrix should be best modeled as the combination of a sparse graph of pairwise partial correlations representing local interactions and a low-rank component representing common fluctuations and external inputs. Indeed, in cross-validation tests, the covariance matrix estimator with this structure consistently outperformed other regularized estimators. The sparse component of the estimate defined a graph of interactions. These interactions reflected the physical distances and orientation tuning properties of cells: The density of positive 'excitatory' interactions decreased rapidly with geometric distances and with differences in orientation preference whereas negative 'inhibitory' interactions were less selective. Because of its superior performance, this 'sparse+latent' estimator likely provides a more physiologically relevant representation of the functional connectivity in densely sampled recordings than the sample correlation matrix. Dimitri Yatsenko, Kresimir Josic, Alexander S. Ecker, Emmanouil Froudarakis, R. James Cotton, Andreas S. Tolias |
PLoS Comput. Biol. | 4 |