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2008


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Variational Bayesian Model Selection in Linear Gaussian State-Space based Models

Chiappa, S.

International Workshop on Flexible Modelling: Smoothing and Robustness (FMSR 2008), 2008, pages: 1, November 2008 (poster)

Web [BibTex]

2008

Web [BibTex]


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Towards the neural basis of the flash-lag effect

Ecker, A., Berens, P., Hoenselaar, A., Subramaniyan, M., Tolias, A., Bethge, M.

International Workshop on Aspects of Adaptive Cortex Dynamics, 2008, pages: 1, September 2008 (poster)

PDF [BibTex]

PDF [BibTex]


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Policy Learning: A Unified Perspective With Applications In Robotics

Peters, J., Kober, J., Nguyen-Tuong, D.

8th European Workshop on Reinforcement Learning for Robotics (EWRL 2008), 8, pages: 10, July 2008 (poster)

Abstract
Policy Learning approaches are among the best suited methods for high-dimensional, continuous control systems such as anthropomorphic robot arms and humanoid robots. In this paper, we show two contributions: firstly, we show a unified perspective which allows us to derive several policy learning al- gorithms from a common point of view, i.e, policy gradient algorithms, natural- gradient algorithms and EM-like policy learning. Secondly, we present several applications to both robot motor primitive learning as well as to robot control in task space. Results both from simulation and several different real robots are shown.

PDF [BibTex]

PDF [BibTex]


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Reinforcement Learning of Perceptual Coupling for Motor Primitives

Kober, J., Peters, J.

8th European Workshop on Reinforcement Learning for Robotics (EWRL 2008), 8, pages: 16, July 2008 (poster)

Abstract
Reinforcement learning is a natural choice for the learning of complex motor tasks by reward-related self-improvement. As the space of movements is high-dimensional and continuous, a policy parametrization is needed which can be used in this context. Traditional motor primitive approaches deal largely with open-loop policies which can only deal with small perturbations. In this paper, we present a new type of motor primitive policies which serve as closed-loop policies together with an appropriate learning algorithm. Our new motor primitives are an augmented version version of the dynamic systems motor primitives that incorporates perceptual coupling to external variables. We show that these motor primitives can perform complex tasks such a Ball-in-a-Cup or Kendama task even with large variances in the initial conditions where a human would hardly be able to learn this task. We initialize the open-loop policies by imitation learning and the perceptual coupling with a handcrafted solution. We first improve the open-loop policies and subsequently the perceptual coupling using a novel reinforcement learning method which is particularly well-suited for motor primitives.

PDF [BibTex]

PDF [BibTex]


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Flexible Models for Population Spike Trains

Bethge, M., Macke, J., Berens, P., Ecker, A., Tolias, A.

AREADNE 2008: Research in Encoding and Decoding of Neural Ensembles, 2, pages: 52, June 2008 (poster)

PDF [BibTex]

PDF [BibTex]


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Pairwise Correlations and Multineuronal Firing Patterns in the Primary Visual Cortex of the Awake, Behaving Macaque

Berens, P., Ecker, A., Subramaniyan, M., Macke, J., Hauck, P., Bethge, M., Tolias, A.

AREADNE 2008: Research in Encoding and Decoding of Neural Ensembles, 2, pages: 48, June 2008 (poster)

PDF [BibTex]

PDF [BibTex]


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Visual saliency re-visited: Center-surround patterns emerge as optimal predictors for human fixation targets

Wichmann, F., Kienzle, W., Schölkopf, B., Franz, M.

Journal of Vision, 8(6):635, 8th Annual Meeting of the Vision Sciences Society (VSS), June 2008 (poster)

Abstract
Humans perceives the world by directing the center of gaze from one location to another via rapid eye movements, called saccades. In the period between saccades the direction of gaze is held fixed for a few hundred milliseconds (fixations). It is primarily during fixations that information enters the visual system. Remarkably, however, after only a few fixations we perceive a coherent, high-resolution scene despite the visual acuity of the eye quickly decreasing away from the center of gaze: This suggests an effective strategy for selecting saccade targets. Top-down effects, such as the observer's task, thoughts, or intentions have an effect on saccadic selection. Equally well known is that bottom-up effects-local image structure-influence saccade targeting regardless of top-down effects. However, the question of what the most salient visual features are is still under debate. Here we model the relationship between spatial intensity patterns in natural images and the response of the saccadic system using tools from machine learning. This allows us to identify the most salient image patterns that guide the bottom-up component of the saccadic selection system, which we refer to as perceptive fields. We show that center-surround patterns emerge as the optimal solution to the problem of predicting saccade targets. Using a novel nonlinear system identification technique we reduce our learned classifier to a one-layer feed-forward network which is surprisingly simple compared to previously suggested models assuming more complex computations such as multi-scale processing, oriented filters and lateral inhibition. Nevertheless, our model is equally predictive and generalizes better to novel image sets. Furthermore, our findings are consistent with neurophysiological hardware in the superior colliculus. Bottom-up visual saliency may thus not be computed cortically as has been thought previously.

Web DOI [BibTex]

Web DOI [BibTex]


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Analysis of Pattern Recognition Methods in Classifying Bold Signals in Monkeys at 7-Tesla

Ku, S., Gretton, A., Macke, J., Tolias, A., Logothetis, N.

AREADNE 2008: Research in Encoding and Decoding of Neural Ensembles, 2, pages: 67, June 2008 (poster)

Abstract
Pattern recognition methods have shown that fMRI data can reveal significant information about brain activity. For example, in the debate of how object-categories are represented in the brain, multivariate analysis has been used to provide evidence of distributed encoding schemes. Many follow-up studies have employed different methods to analyze human fMRI data with varying degrees of success. In this study we compare four popular pattern recognition methods: correlation analysis, support-vector machines (SVM), linear discriminant analysis and Gaussian naïve Bayes (GNB), using data collected at high field (7T) with higher resolution than usual fMRI studies. We investigate prediction performance on single trials and for averages across varying numbers of stimulus presentations. The performance of the various algorithms depends on the nature of the brain activity being categorized: for several tasks, many of the methods work well, whereas for others, no methods perform above chance level. An important factor in overall classification performance is careful preprocessing of the data, including dimensionality reduction, voxel selection, and outlier elimination.

[BibTex]

[BibTex]


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The role of stimulus correlations for population decoding in the retina

Schwartz, G., Macke, J., Berry, M.

Computational and Systems Neuroscience 2008 (COSYNE 2008), 5, pages: 172, March 2008 (poster)

PDF Web [BibTex]

PDF Web [BibTex]

2001


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Perception of Planar Shapes in Depth

Wichmann, F., Willems, B., Rosas, P., Wagemans, J.

Journal of Vision, 1(3):176, First Annual Meeting of the Vision Sciences Society (VSS), December 2001 (poster)

Abstract
We investigated the influence of the perceived 3D-orientation of planar elliptical shapes on the perception of the shapes themselves. Ellipses were projected onto the surface of a sphere and subjects were asked to indicate if the projected shapes looked as if they were a circle on the surface of the sphere. The image of the sphere was obtained from a real, (near) perfect sphere using a highly accurate digital camera (real sphere diameter 40 cm; camera-to-sphere distance 320 cm; for details see Willems et al., Perception 29, S96, 2000; Photometrics SenSys 400 digital camera with Rodenstock lens, 12-bit linear luminance resolution). Stimuli were presented monocularly on a carefully linearized Sony GDM-F500 monitor keeping the scene geometry as in the real case (sphere diameter on screen 8.2 cm; viewing distance 66 cm). Experiments were run in a darkened room using a viewing tube to minimize, as far as possible, extraneous monocular cues to depth. Three different methods were used to obtain subjects' estimates of 3D-shape: the method of adjustment, temporal 2-alternative forced choice (2AFC) and yes/no. Several results are noteworthy. First, mismatch between perceived and objective slant tended to decrease with increasing objective slant. Second, the variability of the settings, too, decreased with increasing objective slant. Finally, we comment on the results obtained using different psychophysical methods and compare our results to those obtained using a real sphere and binocular vision (Willems et al.).

Web DOI [BibTex]

2001

Web DOI [BibTex]


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Plaid maskers revisited: asymmetric plaids

Wichmann, F.

pages: 57, 4. T{\"u}binger Wahrnehmungskonferenz (TWK), March 2001 (poster)

Abstract
A large number of psychophysical and physiological experiments suggest that luminance patterns are independently analysed in channels responding to different bands of spatial frequency. There are, however, interactions among stimuli falling well outside the usual estimates of channels' bandwidths. Derrington & Henning (1989) first reported that, in 2-AFC sinusoidal-grating detection, plaid maskers, whose components are oriented symmetrically about the signal orientation, cause a substantially larger threshold elevation than would be predicted from their sinusoidal constituents alone. Wichmann & Tollin (1997a,b) and Wichmann & Henning (1998) confirmed and extended the original findings, measuring masking as a function of presentation time and plaid mask contrast. Here I investigate masking using plaid patterns whose components are asymmetrically positioned about the signal orientation. Standard temporal 2-AFC pattern discrimination experiments were conducted using plaid patterns and oblique sinusoidal gratings as maskers, and horizontally orientated sinusoidal gratings as signals. Signal and maskers were always interleaved on the display (refresh rate 152 Hz). As in the case of the symmetrical plaid maskers, substantial masking was observed for many of the asymmetrical plaids. Masking is neither a straightforward function of the plaid's constituent sinusoidal components nor of the periodicity of the luminance beats between components. These results cause problems for the notion that, even for simple stimuli, detection and discrimination are based on the outputs of channels tuned to limited ranges of spatial frequency and orientation, even if a limited set of nonlinear interactions between these channels is allowed.

Web [BibTex]

Web [BibTex]


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The pedestal effect with a pulse train and its constituent sinusoids

Henning, G., Wichmann, F., Bird, C.

Twenty-Sixth Annual Interdisciplinary Conference, 2001 (poster)

Abstract
Curves showing "threshold" contrast for detecting a signal grating as a function of the contrast of a masking grating of the same orientation, spatial frequency, and phase show a characteristic improvement in performance at masker contrasts near the contrast threshold of the unmasked signal. Depending on the percentage of correct responses used to define the threshold, the best performance can be as much as a factor of three better than the unmasked threshold obtained in the absence of any masking grating. The result is called the pedestal effect (sometimes, the dipper function). We used a 2AFC procedure to measure the effect with harmonically related sinusoids ranging from 2 to 16 c/deg - all with maskers of the same orientation, spatial frequency and phase - and with masker contrasts ranging from 0 to 50%. The curves for different spatial frequencies are identical if both the vertical axis (showing the threshold signal contrast) and the horizontal axis (showing the masker contrast) are scaled by the threshold contrast of the signal obtained with no masker. Further, a pulse train with a fundamental frequency of 2 c/deg produces a curve that is indistinguishable from that of a 2-c/deg sinusoid despite the fact that at higher masker contrasts, the pulse train contains at least 8 components all of them equally detectable. The effect of adding 1-D spatial noise is also discussed.

[BibTex]

[BibTex]


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Modeling the Dynamics of Individual Neurons of the Stomatogastric Networks with Support Vector Machines

Frontzek, T., Gutzen, C., Lal, TN., Heinzel, H-G., Eckmiller, R., Böhm, H.

Abstract Proceedings of the 6th International Congress of Neuroethology (ICN'2001) Bonn, abstract 404, 2001 (poster)

Abstract
In small rhythmic active networks timing of individual neurons is crucial for generating different spatial-temporal motor patterns. Switching of one neuron between different rhythms can cause transition between behavioral modes. In order to understand the dynamics of rhythmically active neurons we analyzed the oscillatory membranpotential of a pacemaker neuron and used different neural network models to predict dynamics of its time series. In a first step we have trained conventional RBF networks and Support Vector Machines (SVMs) using gaussian kernels with intracellulary recordings of the pyloric dilatator neuron in the Australian crayfish, Cherax destructor albidus. As a rule SVMs were able to learn the nonlinear dynamics of pyloric neurons faster (e.g. 15s) than RBF networks (e.g. 309s) under the same hardware conditions. After training SVMs performed a better iterated one-step-ahead prediction of time series in the pyloric dilatator neuron with regard to test error and error sum. The test error decreased with increasing number of support vectors. The best SVM used 196 support vectors and produced a test error of 0.04622 as opposed to the best RBF with 0.07295 using 26 RBF-neurons. In pacemaker neuron PD the timepoint at which the membranpotential will cross threshold for generation of its oscillatory peak is most important for determination of the test error. Interestingly SVMs are especially better in predicting this important part of the membranpotential which is superimposed by various synaptic inputs, which drive the membranpotential to its threshold.

[BibTex]

[BibTex]

1997


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Masking by plaid patterns is not explained by adaptation, simple contrast gain-control or distortion products

Wichmann, F., Tollin, D.

Investigative Ophthamology and Visual Science, 38 (4), pages: S631, 1997 (poster)

[BibTex]

1997

[BibTex]


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Masking by plaid patterns: spatial frequency tuning and contrast dependency

Wichmann, F., Tollin, D.

OSA Conference Program, pages: 97, 1997 (poster)

Abstract
The detectability of horizontally orientated sinusoidal signals at different spatial-frequencies was measured in standard 2AFC - tasks in the presence of two-component plaid patterns of different orientation and contrast. The shape of the resulting masking surface provides insight into, and constrains models of, the underlying masking mechanisms.

[BibTex]

[BibTex]