scholarly journals Finding Approximate POMDP solutions Through Belief Compression

2005 ◽  
Vol 23 ◽  
pp. 1-40 ◽  
Author(s):  
N. Roy ◽  
G. Gordon ◽  
S. Thrun

Standard value function approaches to finding policies for Partially Observable Markov Decision Processes (POMDPs) are generally considered to be intractable for large models. The intractability of these algorithms is to a large extent a consequence of computing an exact, optimal policy over the entire belief space. However, in real-world POMDP problems, computing the optimal policy for the full belief space is often unnecessary for good control even for problems with complicated policy classes. The beliefs experienced by the controller often lie near a structured, low-dimensional subspace embedded in the high-dimensional belief space. Finding a good approximation to the optimal value function for only this subspace can be much easier than computing the full value function. We introduce a new method for solving large-scale POMDPs by reducing the dimensionality of the belief space. We use Exponential family Principal Components Analysis (Collins, Dasgupta & Schapire, 2002) to represent sparse, high-dimensional belief spaces using small sets of learned features of the belief state. We then plan only in terms of the low-dimensional belief features. By planning in this low-dimensional space, we can find policies for POMDP models that are orders of magnitude larger than models that can be handled by conventional techniques. We demonstrate the use of this algorithm on a synthetic problem and on mobile robot navigation tasks.

Author(s):  
Samuel Melton ◽  
Sharad Ramanathan

Abstract Motivation Recent technological advances produce a wealth of high-dimensional descriptions of biological processes, yet extracting meaningful insight and mechanistic understanding from these data remains challenging. For example, in developmental biology, the dynamics of differentiation can now be mapped quantitatively using single-cell RNA sequencing, yet it is difficult to infer molecular regulators of developmental transitions. Here, we show that discovering informative features in the data is crucial for statistical analysis as well as making experimental predictions. Results We identify features based on their ability to discriminate between clusters of the data points. We define a class of problems in which linear separability of clusters is hidden in a low-dimensional space. We propose an unsupervised method to identify the subset of features that define a low-dimensional subspace in which clustering can be conducted. This is achieved by averaging over discriminators trained on an ensemble of proposed cluster configurations. We then apply our method to single-cell RNA-seq data from mouse gastrulation, and identify 27 key transcription factors (out of 409 total), 18 of which are known to define cell states through their expression levels. In this inferred subspace, we find clear signatures of known cell types that eluded classification prior to discovery of the correct low-dimensional subspace. Availability and implementation https://github.com/smelton/SMD. Supplementary information Supplementary data are available at Bioinformatics online.


2021 ◽  
Author(s):  
Corson N Areshenkoff ◽  
Daniel J Gale ◽  
Joe Y Nashed ◽  
Dominic Standage ◽  
John Randall Flanagan ◽  
...  

Humans vary greatly in their motor learning abilities, yet little is known about the neural mechanisms that underlie this variability. Recent neuroimaging and electrophysiological studies demonstrate that large-scale neural dynamics inhabit a low-dimensional subspace or manifold, and that learning is constrained by this intrinsic manifold architecture. Here we asked, using functional MRI, whether subject-level differences in neural excursion from manifold structure can explain differences in learning across participants. We had subjects perform a sensorimotor adaptation task in the MRI scanner on two consecutive days, allowing us to assess their learning performance across days, as well as continuously measure brain activity. We find that the overall neural excursion from manifold activity in both cognitive and sensorimotor brain networks is associated with differences in subjects' patterns of learning and relearning across days. These findings suggest that off-manifold activity provides an index of the relative engagement of different neural systems during learning, and that intersubject differences in patterns of learning and relearning across days are related to reconfiguration processes in cognitive and sensorimotor networks during learning.


Author(s):  
Akira Imakura ◽  
Momo Matsuda ◽  
Xiucai Ye ◽  
Tetsuya Sakurai

Dimensionality reduction methods that project highdimensional data to a low-dimensional space by matrix trace optimization are widely used for clustering and classification. The matrix trace optimization problem leads to an eigenvalue problem for a low-dimensional subspace construction, preserving certain properties of the original data. However, most of the existing methods use only a few eigenvectors to construct the low-dimensional space, which may lead to a loss of useful information for achieving successful classification. Herein, to overcome the deficiency of the information loss, we propose a novel complex moment-based supervised eigenmap including multiple eigenvectors for dimensionality reduction. Furthermore, the proposed method provides a general formulation for matrix trace optimization methods to incorporate with ridge regression, which models the linear dependency between covariate variables and univariate labels. To reduce the computational complexity, we also propose an efficient and parallel implementation of the proposed method. Numerical experiments indicate that the proposed method is competitive compared with the existing dimensionality reduction methods for the recognition performance. Additionally, the proposed method exhibits high parallel efficiency.


2015 ◽  
Vol 26 (09) ◽  
pp. 1550103
Author(s):  
Yifang Ma ◽  
Zhiming Zheng

The evolution of networks or dynamic systems is controlled by many parameters in high-dimensional space, and it is crucial to extract the reduced and dominant ones in low-dimensional space. Here we consider the network ensemble, introduce a matrix resolvent scale function and apply it to a spectral approach to get the similarity relations between each pair of networks. The concept of Diffusion Maps is used to get the principal parameters, and we point out that the reduced dimensional principal parameters are captured by the low order eigenvectors of the diffusion matrix of the network ensemble. We validate our results by using two classical network ensembles and one dynamical network sequence via a cooperative Achlioptas growth process where an abrupt transition of the structures has been captured by our method. Our method provides a potential access to the pursuit of invisible control parameters of complex systems.


2009 ◽  
Vol 2009 ◽  
pp. 1-8 ◽  
Author(s):  
Eimad E. Abusham ◽  
E. K. Wong

A novel method based on the local nonlinear mapping is presented in this research. The method is called Locally Linear Discriminate Embedding (LLDE). LLDE preserves a local linear structure of a high-dimensional space and obtains a compact data representation as accurately as possible in embedding space (low dimensional) before recognition. For computational simplicity and fast processing, Radial Basis Function (RBF) classifier is integrated with the LLDE. RBF classifier is carried out onto low-dimensional embedding with reference to the variance of the data. To validate the proposed method, CMU-PIE database has been used and experiments conducted in this research revealed the efficiency of the proposed methods in face recognition, as compared to the linear and non-linear approaches.


2017 ◽  
Author(s):  
Peiran Gao ◽  
Eric Trautmann ◽  
Byron Yu ◽  
Gopal Santhanam ◽  
Stephen Ryu ◽  
...  

AbstractIn many experiments, neuroscientists tightly control behavior, record many trials, and obtain trial-averaged firing rates from hundreds of neurons in circuits containing billions of behaviorally relevant neurons. Di-mensionality reduction methods reveal a striking simplicity underlying such multi-neuronal data: they can be reduced to a low-dimensional space, and the resulting neural trajectories in this space yield a remarkably insightful dynamical portrait of circuit computation. This simplicity raises profound and timely conceptual questions. What are its origins and its implications for the complexity of neural dynamics? How would the situation change if we recorded more neurons? When, if at all, can we trust dynamical portraits obtained from measuring an infinitesimal fraction of task relevant neurons? We present a theory that answers these questions, and test it using physiological recordings from reaching monkeys. This theory reveals conceptual insights into how task complexity governs both neural dimensionality and accurate recovery of dynamic portraits, thereby providing quantitative guidelines for future large-scale experimental design.


2021 ◽  
Vol 12 ◽  
Author(s):  
Jianping Zhao ◽  
Na Wang ◽  
Haiyun Wang ◽  
Chunhou Zheng ◽  
Yansen Su

Dimensionality reduction of high-dimensional data is crucial for single-cell RNA sequencing (scRNA-seq) visualization and clustering. One prominent challenge in scRNA-seq studies comes from the dropout events, which lead to zero-inflated data. To address this issue, in this paper, we propose a scRNA-seq data dimensionality reduction algorithm based on a hierarchical autoencoder, termed SCDRHA. The proposed SCDRHA consists of two core modules, where the first module is a deep count autoencoder (DCA) that is used to denoise data, and the second module is a graph autoencoder that projects the data into a low-dimensional space. Experimental results demonstrate that SCDRHA has better performance than existing state-of-the-art algorithms on dimension reduction and noise reduction in five real scRNA-seq datasets. Besides, SCDRHA can also dramatically improve the performance of data visualization and cell clustering.


Author(s):  
Jing Wang ◽  
Jinglin Zhou ◽  
Xiaolu Chen

AbstractIndustrial data variables show obvious high dimension and strong nonlinear correlation. Traditional multivariate statistical monitoring methods, such as PCA, PLS, CCA, and FDA, are only suitable for solving the high-dimensional data processing with linear correlation. The kernel mapping method is the most common technique to deal with the nonlinearity, which projects the original data in the low-dimensional space to the high-dimensional space through appropriate kernel functions so as to achieve the goal of linear separability in the new space. However, the space projection from the low dimension to the high dimension is contradictory to the actual requirement of dimensionality reduction of the data. So kernel-based method inevitably increases the complexity of data processing.


2018 ◽  
Author(s):  
Damon H. May ◽  
Jeffrey Bilmes ◽  
William S. Noble

AbstractDespite an explosion of data in public repositories, peptide mass spectra are usually analyzed by each laboratory in isolation, treating each experiment as if it has no relationship to any others. This approach fails to exploit the wealth of existing, previously analyzed mass spectrometry data. Others have jointly analyzed many mass spectra, often using clustering. However, mass spectra are not necessarily best summarized as clusters, and although new spectra can be added to existing clusters, clustering methods previously applied to mass spectra do not allow new clusters to be defined without completely re-clustering. As an alternative, we propose to train a deep neural network, called “GLEAMS,” to learn an embedding of spectra into a low-dimensional space in which spectra generated by the same peptide are close to one another. We demonstrate empirically the utility of this learned embedding by propagating annotations from labeled to unlabeled spectra. We further use GLEAMS to detect groups of unidentified, proximal spectra representing the same peptide, and we show how to use these spectral communities to reveal misidentified spectra and to characterize frequently observed but consistently unidentified molecular species. We provide a software implementation of our approach, along with a tool to quickly embed additional spectra using a pre-trained model, to facilitate large-scale analyses.


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