There has been a recent push in extraction of 3D spatial layout of scenes.

We describe a neuromorphic chip transistor heterogeneity, introduced by the fabrication process, to generate orientation maps similar to those imaged in vivo. Our model consists of a recurrent network of excitatory and inhibitory cells in parallel with a push-pull stage. Similar to a previous model the recurrent network displays hotspots of activity that give rise to visual feature maps. Unlike previous work, however, the map for orientation does not depend on the sign of contrast. Instead, sign- independent cells driven by both ON and OFF channels anchor the map, while push-pull interactions give rise to sign-preserving cells.

Conventional 3D human pose estimation relies on first detecting 2D body keypoints and then solving the 2D to 3D correspondence problem.Despite the promising results, this learning paradigm is highly dependent on the quality of the 2D keypoint detector, which is inevitably fragile to occlusions and out-of-image absences.In this paper,we propose a novel Pose Orientation Net (PONet) that is able to robustly estimate 3D pose by learning orientations only, hence bypassing the error-prone keypoint detector in the absence of image evidence. For images with partially invisible limbs, PONet estimates the 3D orientation of these limbs by taking advantage of the local image evidence to recover the 3D pose.Moreover, PONet is competent to infer full 3D poses even from images with completely invisible limbs, by exploiting the orientation correlation between visible limbs to complement the estimated poses,further improving the robustness of 3D pose estimation.We evaluate our method on multiple datasets, including Human3.6M, MPII, MPI-INF-3DHP, and 3DPW. Our method achieves results on par with state-of-the-art techniques in ideal settings, yet significantly eliminates the dependency on keypoint detectors and the corresponding computation burden. In highly challenging scenarios, such as truncation and erasing, our method performs very robustly and yields much superior results as compared to state of the art,demonstrating its potential for real-world applications.

There has been a recent push in extraction of 3D spatial layout of scenes. However, none of these approaches model the 3D interaction between objects and the spatial layout. In this paper, we argue for a parametric representation of objects in 3D, which allows us to incorporate volumetric constraints of the physical world. We show that augmenting current structured prediction techniques with volumetric reasoning significantly improves the performance of the state-of-the-art.

A method for computing the rarity of latent fingerprints represented by minutiae is given. It allows determining the probability of finding a match for an evidence print in a database of n known prints. The probability of random correspondence between evidence and database is determined in three procedural steps. In the registration step the latent print is aligned by finding its core point; which is done using a procedure based on a machine learning approach based on Gaussian processes. In the evidence probability evaluation step a generative model based on Bayesian networks is used to determine the probability of the evidence; it takes into account both the dependency of each minutia on nearby minutiae and the confidence of their presence in the evidence. In the specific probability of random correspondence step the evidence probability is used to determine the probability of match among n for a given tolerance; the last evaluation is similar to the birthday correspondence probability for a specific birthday. The generative model is validated using a goodness-of-fit test evaluated with a standard database of fingerprints. The probability of random correspondence for several latent fingerprints are evaluated for varying numbers of minutiae.

One major role of primary visual cortex (V1) in vision is the encoding of the orientation of lines and contours. The role of the local recurrent network in these computations is, however, still a matter of debate. To address this issue, we analyze intracellular recording data of cat V1, which combine measuring the tuning of a range of neuronal properties with a precise localization of the recording sites in the orientation preference map. For the analysis, we consider a network model of Hodgkin-Huxley type neurons arranged according to a biologically plausible two-dimensional topographic orientation preference map. We then systematically vary the strength of the recurrent excitation and inhibition relative to the strength of the afferent input. Each parametrization gives rise to a different model instance for which the tuning of model neurons at different locations of the orientation map is compared to the experimentally measured orientation tuning of membrane potential, spike output, excitatory, and inhibitory conductances. A quantitative analysis shows that the data provides strong evidence for a network model in which the afferent input is dominated by strong, balanced contributions of recurrent excitation and inhibition. This recurrent regime is close to a regime of 'instability', where strong, self-sustained activity of the network occurs. The firing rate of neurons in the best-fitting network is particularly sensitive to small modulations of model parameters, which could be one of the functional benefits of a network operating in this particular regime.

We describe a neuromorphic chip that utilizes transistor heterogeneity, introduced by the fabrication process, to generate orientation maps similar to those imaged in vivo. Our model consists of a recurrent network of excitatory and inhibitory cells in parallel with a push-pull stage. Similar to a previous model the recurrent network displays hotspots of activity that give rise to visual feature maps. Unlike previous work, however, the map for orientation does not depend on the sign of contrast.

We describe a neuromorphic chip that utilizes transistor heterogeneity, introduced by the fabrication process, to generate orientation maps similar to those imaged in vivo. Our model consists of a recurrent network of excitatory and inhibitory cells in parallel with a push-pull stage. Similar to a previous model the recurrent network displays hotspots of activity that give rise to visual feature maps. Unlike previous work, however, the map for orientation does not depend on the sign of contrast.

We describe a neuromorphic chip that utilizes transistor heterogeneity, introduced by the fabrication process, to generate orientation maps similar to those imaged in vivo. Our model consists of a recurrent network of excitatory and inhibitory cells in parallel with a push-pull stage. Similar to a previous model the recurrent network displays hotspots of activity that give rise to visual feature maps. Unlike previous work, however, the map for orientation does not depend on the sign of contrast. Instead, signindependent cellsdriven by both ON and OFF channels anchor the map, while push-pull interactions give rise to sign-preserving cells. These two groups of orientation-selective cells are similar to complex and simple cells observed in V1.

More than ten of the most prominent models for the structure and for the activity dependent formation of orientation and ocular dominance columns in the striate cort( x have been evaluated. We implemented those models on parallel machines, we extensively explored parameter space, and we quantitatively compared model predictions with experimental data which were recorded optically from macaque striate cortex. In our contribution we present a summary of our results to date. Briefly, we find that (i) despite apparent differences, many models are based on similar principles and, consequently, make similar predictions, (ii) certain "pattern models" as well as the developmental "correlation-based learning" models disagree with the experimental data, and (iii) of the models we have investigated, "competitive Hebbian" models and the recent model of Swindale provide the best match with experimental data. 1 Models and Data The models for the formation and structure of orientation and ocular dominance columns which we have investigated are summarized in table 1. Models fall into two categories: "Pattern models" whose aim is to achieve a concise description of the observed patterns and "developmental models" which are focussed on the pro- 94