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Dive into the research topics where Jonathon Shlens is active.

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Featured researches published by Jonathon Shlens.


computer vision and pattern recognition | 2016

Rethinking the Inception Architecture for Computer Vision

Christian Szegedy; Vincent Vanhoucke; Sergey Ioffe; Jonathon Shlens; Zbigniew Wojna

Convolutional networks are at the core of most state of-the-art computer vision solutions for a wide variety of tasks. Since 2014 very deep convolutional networks started to become mainstream, yielding substantial gains in various benchmarks. Although increased model size and computational cost tend to translate to immediate quality gains for most tasks (as long as enough labeled data is provided for training), computational efficiency and low parameter count are still enabling factors for various use cases such as mobile vision and big-data scenarios. Here we are exploring ways to scale up networks in ways that aim at utilizing the added computation as efficiently as possible by suitably factorized convolutions and aggressive regularization. We benchmark our methods on the ILSVRC 2012 classification challenge validation set demonstrate substantial gains over the state of the art: 21:2% top-1 and 5:6% top-5 error for single frame evaluation using a network with a computational cost of 5 billion multiply-adds per inference and with using less than 25 million parameters. With an ensemble of 4 models and multi-crop evaluation, we report 3:5% top-5 error and 17:3% top-1 error on the validation set and 3:6% top-5 error on the official test set.


Nature | 2008

Spatio-temporal correlations and visual signalling in a complete neuronal population

Jonathan W. Pillow; Jonathon Shlens; Liam Paninski; Alexander Sher; Alan Litke; E. J. Chichilnisky; Eero P. Simoncelli

Statistical dependencies in the responses of sensory neurons govern both the amount of stimulus information conveyed and the means by which downstream neurons can extract it. Although a variety of measurements indicate the existence of such dependencies, their origin and importance for neural coding are poorly understood. Here we analyse the functional significance of correlated firing in a complete population of macaque parasol retinal ganglion cells using a model of multi-neuron spike responses. The model, with parameters fit directly to physiological data, simultaneously captures both the stimulus dependence and detailed spatio-temporal correlations in population responses, and provides two insights into the structure of the neural code. First, neural encoding at the population level is less noisy than one would expect from the variability of individual neurons: spike times are more precise, and can be predicted more accurately when the spiking of neighbouring neurons is taken into account. Second, correlations provide additional sensory information: optimal, model-based decoding that exploits the response correlation structure extracts 20% more information about the visual scene than decoding under the assumption of independence, and preserves 40% more visual information than optimal linear decoding. This model-based approach reveals the role of correlated activity in the retinal coding of visual stimuli, and provides a general framework for understanding the importance of correlated activity in populations of neurons.


The Journal of Neuroscience | 2006

The Structure of Multi-Neuron Firing Patterns in Primate Retina

Jonathon Shlens; Greg D. Field; Jeffrey L. Gauthier; Matthew I. Grivich; Dumitru Petrusca; Alexander Sher; Alan Litke; E. J. Chichilnisky

Current understanding of many neural circuits is limited by our ability to explore the vast number of potential interactions between different cells. We present a new approach that dramatically reduces the complexity of this problem. Large-scale multi-electrode recordings were used to measure electrical activity in nearly complete, regularly spaced mosaics of several hundred ON and OFF parasol retinal ganglion cells in macaque monkey retina. Parasol cells exhibited substantial pairwise correlations, as has been observed in other species, indicating functional connectivity. However, pairwise measurements alone are insufficient to determine the prevalence of multi-neuron firing patterns, which would be predicted from widely diverging common inputs and have been hypothesized to convey distinct visual messages to the brain. The number of possible multi-neuron firing patterns is far too large to study exhaustively, but this problem may be circumvented if two simple rules of connectivity can be established: (1) multi-cell firing patterns arise from multiple pairwise interactions, and (2) interactions are limited to adjacent cells in the mosaic. Using maximum entropy methods from statistical mechanics, we show that pairwise and adjacent interactions accurately accounted for the structure and prevalence of multi-neuron firing patterns, explaining ∼98% of the departures from statistical independence in parasol cells and ∼99% of the departures that were reproducible in repeated measurements. This approach provides a way to define limits on the complexity of network interactions and thus may be relevant for probing the function of many neural circuits.


computer vision and pattern recognition | 2013

Fast, Accurate Detection of 100,000 Object Classes on a Single Machine

Thomas Dean; Mark A. Ruzon; Mark Segal; Jonathon Shlens; Sudheendra Vijayanarasimhan; Jay Yagnik

Many object detection systems are constrained by the time required to convolve a target image with a bank of filters that code for different aspects of an objects appearance, such as the presence of component parts. We exploit locality-sensitive hashing to replace the dot-product kernel operator in the convolution with a fixed number of hash-table probes that effectively sample all of the filter responses in time independent of the size of the filter bank. To show the effectiveness of the technique, we apply it to evaluate 100,000 deformable-part models requiring over a million (part) filters on multiple scales of a target image in less than 20 seconds using a single multi-core processor with 20GB of RAM. This represents a speed-up of approximately 20,000 times - four orders of magnitude - when compared with performing the convolutions explicitly on the same hardware. While mean average precision over the full set of 100,000 object classes is around 0.16 due in large part to the challenges in gathering training data and collecting ground truth for so many classes, we achieve a mAP of at least 0.20 on a third of the classes and 0.30 or better on about 20% of the classes.


Nature | 2010

Functional connectivity in the retina at the resolution of photoreceptors.

Greg D. Field; Jeffrey L. Gauthier; Alexander Sher; Martin Greschner; Timothy A. Machado; Lauren H. Jepson; Jonathon Shlens; Deborah E. Gunning; Keith Mathieson; W. Dabrowski; Liam Paninski; Alan Litke; E. J. Chichilnisky

To understand a neural circuit requires knowledge of its connectivity. Here we report measurements of functional connectivity between the input and ouput layers of the macaque retina at single-cell resolution and the implications of these for colour vision. Multi-electrode technology was used to record simultaneously from complete populations of the retinal ganglion cell types (midget, parasol and small bistratified) that transmit high-resolution visual signals to the brain. Fine-grained visual stimulation was used to identify the location, type and strength of the functional input of each cone photoreceptor to each ganglion cell. The populations of ON and OFF midget and parasol cells each sampled the complete population of long- and middle-wavelength-sensitive cones. However, only OFF midget cells frequently received strong input from short-wavelength-sensitive cones. ON and OFF midget cells showed a small non-random tendency to selectively sample from either long- or middle-wavelength-sensitive cones to a degree not explained by clumping in the cone mosaic. These measurements reveal computations in a neural circuit at the elementary resolution of individual neurons.


The Journal of Neuroscience | 2009

The structure of large-scale synchronized firing in primate retina.

Jonathon Shlens; Greg D. Field; Jeffrey L. Gauthier; Martin Greschner; Alexander Sher; Alan Litke; E. J. Chichilnisky

Synchronized firing among neurons has been proposed to constitute an elementary aspect of the neural code in sensory and motor systems. However, it remains unclear how synchronized firing affects the large-scale patterns of activity and redundancy of visual signals in a complete population of neurons. We recorded simultaneously from hundreds of retinal ganglion cells in primate retina, and examined synchronized firing in completely sampled populations of ∼50–100 ON-parasol cells, which form a major projection to the magnocellular layers of the lateral geniculate nucleus. Synchronized firing in pairs of cells was a subset of a much larger pattern of activity that exhibited local, isotropic spatial properties. However, a simple model based solely on interactions between adjacent cells reproduced 99% of the spatial structure and scale of synchronized firing. No more than 20% of the variability in firing of an individual cell was predictable from the activity of its neighbors. These results held both for spontaneous firing and in the presence of independent visual modulation of the firing of each cell. In sum, large-scale synchronized firing in the entire population of ON-parasol cells appears to reflect simple neighbor interactions, rather than a unique visual signal or a highly redundant coding scheme.


The Journal of Neuroscience | 2007

Spatial Properties and Functional Organization of Small Bistratified Ganglion Cells in Primate Retina

Greg D. Field; Alexander Sher; Jeffrey L. Gauthier; Martin Greschner; Jonathon Shlens; Alan Litke; E. J. Chichilnisky

The primate visual system consists of parallel pathways initiated by distinct cell types in the retina that encode different features of the visual scene. Small bistratified cells (SBCs), which form a major projection to the thalamus, exhibit blue-ON/yellow-OFF [S-ON/(L+M)-OFF] light responses thought to be important for high-acuity color vision. However, the spatial processing properties of individual SBCs and their spatial arrangement across the visual field are poorly understood. The present study of peripheral primate retina reveals that contrary to previous suggestions, SBCs exhibit center-surround spatial structure, with the (L+M)-OFF component of the receptive field ∼50% larger in diameter than the S-ON component. Analysis of response kinetics shows that the (L+M)-OFF response in SBCs is slower than the S-ON response and significantly less transient than that of simultaneously recorded OFF-parasol cells. The (L+M)-OFF response in SBCs was eliminated by bath application of the metabotropic glutamate receptor agonist l-APB. These observations indicate that the (L+M)-OFF response of SBCs is not formed by OFF-bipolar cell input as has been suspected and suggest that it arises from horizontal cell feedback. Finally, the receptive fields of SBCs form orderly mosaics, with overlap and regularity similar to those of ON-parasol cells. Thus, despite their distinctive morphology and chromatic properties, SBCs exhibit two features of other retinal ganglion cell types: center-surround antagonism and regular mosaic sampling of visual space.


The Journal of Neuroscience | 2007

Identification and Characterization of a Y-Like Primate Retinal Ganglion Cell Type

Dumitru Petrusca; Matthew I. Grivich; Alexander Sher; Greg D. Field; Jeffrey L. Gauthier; Martin Greschner; Jonathon Shlens; E. J. Chichilnisky; Alan Litke

The primate retina communicates visual information to the brain via a set of parallel pathways that originate from at least 22 anatomically distinct types of retinal ganglion cells. Knowledge of the physiological properties of these ganglion cell types is of critical importance for understanding the functioning of the primate visual system. Nonetheless, the physiological properties of only a handful of retinal ganglion cell types have been studied in detail. Here we show, using a newly developed multielectrode array system for the large-scale recording of neural activity, the existence of a physiologically distinct population of ganglion cells in the primate retina with distinctive visual response properties. These cells, which we will refer to as upsilon cells, are characterized by large receptive fields, rapid and transient responses to light, and significant nonlinearities in their spatial summation. Based on the measured properties of these cells, we speculate that they correspond to the smooth/large radiate cells recently identified morphologically in the primate retina and may therefore provide visual input to both the lateral geniculate nucleus and the superior colliculus. We further speculate that the upsilon cells may be the primate retinas counterparts of the Y-cells observed in the cat and other mammalian species.


Neural Computation | 2005

Estimating Entropy Rates with Bayesian Confidence Intervals

Matthew B. Kennel; Jonathon Shlens; Henry D. I. Abarbanel; E. J. Chichilnisky

The entropy rate quantifies the amount of uncertainty or disorder produced by any dynamical system. In a spiking neuron, this uncertainty translates into the amount of information potentially encoded and thus the subject of intense theoretical and experimental investigation. Estimating this quantity in observed, experimental data is difficult and requires a judicious selection of probabilistic models, balancing between two opposing biases. We use a model weighting principle originally developed for lossless data compression, following the minimum description length principle. This weighting yields a direct estimator of the entropy rate, which, compared to existing methods, exhibits significantly less bias and converges faster in simulation. With Monte Carlo techinques, we estimate a Bayesian confidence interval for the entropy rate. In related work, weap-ply these ideas to estimate the information rates between sensory stimuli and neural responses in experimental data (Shlens, Kennel, Abarbanel, & Chichilnisky, in preparation).


Journal of Computational Neuroscience | 2012

Modeling the impact of common noise inputs on the network activity of retinal ganglion cells

Michael Vidne; Yashar Ahmadian; Jonathon Shlens; Jonathan W. Pillow; Jayant E. Kulkarni; Alan Litke; E. J. Chichilnisky; Eero P. Simoncelli; Liam Paninski

Synchronized spontaneous firing among retinal ganglion cells (RGCs), on timescales faster than visual responses, has been reported in many studies. Two candidate mechanisms of synchronized firing include direct coupling and shared noisy inputs. In neighboring parasol cells of primate retina, which exhibit rapid synchronized firing that has been studied extensively, recent experimental work indicates that direct electrical or synaptic coupling is weak, but shared synaptic input in the absence of modulated stimuli is strong. However, previous modeling efforts have not accounted for this aspect of firing in the parasol cell population. Here we develop a new model that incorporates the effects of common noise, and apply it to analyze the light responses and synchronized firing of a large, densely-sampled network of over 250 simultaneously recorded parasol cells. We use a generalized linear model in which the spike rate in each cell is determined by the linear combination of the spatio-temporally filtered visual input, the temporally filtered prior spikes of that cell, and unobserved sources representing common noise. The model accurately captures the statistical structure of the spike trains and the encoding of the visual stimulus, without the direct coupling assumption present in previous modeling work. Finally, we examined the problem of decoding the visual stimulus from the spike train given the estimated parameters. The common-noise model produces Bayesian decoding performance as accurate as that of a model with direct coupling, but with significantly more robustness to spike timing perturbations.

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Alan Litke

University of California

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Jeffrey L. Gauthier

Salk Institute for Biological Studies

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Martin Greschner

Salk Institute for Biological Studies

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Eero P. Simoncelli

Howard Hughes Medical Institute

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