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1.
Neural Netw ; 41: 39-50, 2013 May.
Article in English | MEDLINE | ID: mdl-23266481

ABSTRACT

This is a simulation-based contribution exploring a novel approach to the open-ended formation of multimodal representations in autonomous agents. In particular, we address the issue of transferring ("bootstrapping") feature selectivities between two modalities, from a previously learned or innate reference representation to a new induced representation. We demonstrate the potential of this algorithm by several experiments with synthetic inputs modeled after a robotics scenario where multimodal object representations are "bootstrapped" from a (reference) representation of object affordances. We focus on typical challenges in autonomous agents: absence of human supervision, changing environment statistics and limited computing power. We propose an autonomous and local neural learning algorithm termed PROPRE (projection-prediction) that updates induced representations based on predictability: competitive advantages are given to those feature-sensitive elements that are inferable from activities in the reference representation. PROPRE implements a bi-directional interaction of clustering ("projection") and inference ("prediction"), the key ingredient being an efficient online measure of predictability controlling learning in the projection step. We show that the proposed method is computationally efficient and stable, and that the multimodal transfer of feature selectivity is successful and robust under resource constraints. Furthermore, we successfully demonstrate robustness to noisy reference representations, non-stationary input statistics and uninformative inputs.


Subject(s)
Artificial Intelligence , Models, Neurological , Neural Networks, Computer , Robotics/methods , Sensory Receptor Cells/physiology , Algorithms , Humans , Proprioception/physiology
2.
Cognit Comput ; 3(1): 146-166, 2011 Mar.
Article in English | MEDLINE | ID: mdl-21475682

ABSTRACT

In this contribution, we present a large-scale hierarchical system for object detection fusing bottom-up (signal-driven) processing results with top-down (model or task-driven) attentional modulation. Specifically, we focus on the question of how the autonomous learning of invariant models can be embedded into a performing system and how such models can be used to define object-specific attentional modulation signals. Our system implements bi-directional data flow in a processing hierarchy. The bottom-up data flow proceeds from a preprocessing level to the hypothesis level where object hypotheses created by exhaustive object detection algorithms are represented in a roughly retinotopic way. A competitive selection mechanism is used to determine the most confident hypotheses, which are used on the system level to train multimodal models that link object identity to invariant hypothesis properties. The top-down data flow originates at the system level, where the trained multimodal models are used to obtain space- and feature-based attentional modulation signals, providing biases for the competitive selection process at the hypothesis level. This results in object-specific hypothesis facilitation/suppression in certain image regions which we show to be applicable to different object detection mechanisms. In order to demonstrate the benefits of this approach, we apply the system to the detection of cars in a variety of challenging traffic videos. Evaluating our approach on a publicly available dataset containing approximately 3,500 annotated video images from more than 1 h of driving, we can show strong increases in performance and generalization when compared to object detection in isolation. Furthermore, we compare our results to a late hypothesis rejection approach, showing that early coupling of top-down and bottom-up information is a favorable approach especially when processing resources are constrained.

3.
BMC Bioinformatics ; 9: 369, 2008 Sep 10.
Article in English | MEDLINE | ID: mdl-18783607

ABSTRACT

BACKGROUND: Exonic splicing enhancers (ESEs) activate nearby splice sites and promote the inclusion (vs. exclusion) of exons in which they reside, while being a binding site for SR proteins. To study the impact of ESEs on alternative splicing it would be useful to have a possibility to detect them in exons. Identifying SR protein-binding sites in human DNA sequences by machine learning techniques is a formidable task, since the exon sequences are also constrained by their functional role in coding for proteins. RESULTS: The choice of training examples needed for machine learning approaches is difficult since there are only few exact locations of human ESEs described in the literature which could be considered as positive examples. Additionally, it is unclear which sequences are suitable as negative examples. Therefore, we developed a motif-oriented data-extraction method that extracts exon sequences around experimentally or theoretically determined ESE patterns. Positive examples are restricted by heuristics based on known properties of ESEs, e.g. location in the vicinity of a splice site, whereas negative examples are taken in the same way from the middle of long exons. We show that a suitably chosen SVM using optimized sequence kernels (e.g., combined oligo kernel) can extract meaningful properties from these training examples. Once the classifier is trained, every potential ESE sequence can be passed to the SVM for verification. Using SVMs with the combined oligo kernel yields a high accuracy of about 90 percent and well interpretable parameters. CONCLUSION: The motif-oriented data-extraction method seems to produce consistent training and test data leading to good classification rates and thus allows verification of potential ESE motifs. The best results were obtained using an SVM with the combined oligo kernel, while oligo kernels with oligomers of a certain length could be used to extract relevant features.


Subject(s)
Algorithms , Artificial Intelligence , Exons/genetics , Pattern Recognition, Automated/methods , RNA Splice Sites/genetics , RNA Splicing/genetics , Sequence Analysis, DNA/methods , Base Sequence , Molecular Sequence Data
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