arXiv subjects

Alfred O. Hero III

Publications and source records attributed to Alfred O. Hero III.

104 records · Page 6Linked to original sources

arXiv2011

Performance Bounds for Sparse Parametric Covariance Estimation in Gaussian Models

We consider estimation of a sparse parameter vector that determines the covariance matrix of a Gaussian random vector via a sparse expansion into known "basis matrices". Using the theory of reproducing kernel Hilbert spaces, we derive lower bounds on the variance of estimators with a given mean function. This includes unbiased estimation as a special case. We also present a numerical comparison of our lower bounds with the variance of two standard estimators (hard-thresholding estimator and maximum likelihood estimator).

cs.IT↗

arXiv2010

Robust Shrinkage Estimation of High-dimensional Covariance Matrices

We address high dimensional covariance estimation for elliptical distributed samples, which are also known as spherically invariant random vectors (SIRV) or compound-Gaussian processes. Specifically we consider shrinkage methods that are suitable for high dimensional problems with a small number of samples (large $p$ small $n$). We start from a classical robust covariance estimator [Tyler(1987)], which is distribution-free within the family of elliptical distribution but inapplicable when $n<p$. Using a shrinkage coefficient, we regularize Tyler's fixed point iterations. We prove that, for all $n$ and $p$, the proposed fixed point iterations converge to a unique limit regardless of the initial condition. Next, we propose a simple, closed-form and data dependent choice for the shrinkage coefficient, which is based on a minimum mean squared error framework. Simulations demonstrate that the proposed method achieves low estimation error and is robust to heavy-tailed samples. Finally, as a real world application we demonstrate the performance of the proposed technique in the context of activity/intrusion detection using a wireless sensor network.

stat.ME↗

arXiv2010

Spatio-Temporal Graphical Model Selection

We consider the problem of estimating the topology of spatial interactions in a discrete state, discrete time spatio-temporal graphical model where the interactions affect the temporal evolution of each agent in a network. Among other models, the susceptible, infected, recovered ($SIR$) model for interaction events fall into this framework. We pose the problem as a structure learning problem and solve it using an $\ell_1$-penalized likelihood convex program. We evaluate the solution on a simulated spread of infectious over a complex network. Our topology estimates outperform those of a standard spatial Markov random field graphical model selection using $\ell_1$-regularized logistic regression.

stat.ML↗

arXiv2009

Shrinkage Algorithms for MMSE Covariance Estimation

We address covariance estimation in the sense of minimum mean-squared error (MMSE) for Gaussian samples. Specifically, we consider shrinkage methods which are suitable for high dimensional problems with a small number of samples (large p small n). First, we improve on the Ledoit-Wolf (LW) method by conditioning on a sufficient statistic. By the Rao-Blackwell theorem, this yields a new estimator called RBLW, whose mean-squared error dominates that of LW for Gaussian variables. Second, to further reduce the estimation error, we propose an iterative approach which approximates the clairvoyant shrinkage estimator. Convergence of this iterative method is established and a closed form expression for the limit is determined, which is referred to as the oracle approximating shrinkage (OAS) estimator. Both RBLW and OAS estimators have simple expressions and are easily implemented. Although the two methods are developed from different persepctives, their structure is identical up to specified constants. The RBLW estimator provably dominates the LW method. Numerical simulations demonstrate that the OAS approach can perform even better than RBLW, especially when n is much less than p. We also demonstrate the performance of these techniques in the context of adaptive beamforming.

stat.ME↗

arXiv2009

Percolation Thresholds of Updated Posteriors for Tracking Causal Markov Processes in Complex Networks

Percolation on complex networks has been used to study computer viruses, epidemics, and other casual processes. Here, we present conditions for the existence of a network specific, observation dependent, phase transition in the updated posterior of node states resulting from actively monitoring the network. Since traditional percolation thresholds are derived using observation independent Markov chains, the threshold of the posterior should more accurately model the true phase transition of a network, as the updated posterior more accurately tracks the process. These conditions should provide insight into modeling the dynamic response of the updated posterior to active intervention and control policies while monitoring large complex networks.

stat.ML↗

arXiv2009

Covariance estimation in decomposable Gaussian graphical models

Graphical models are a framework for representing and exploiting prior conditional independence structures within distributions using graphs. In the Gaussian case, these models are directly related to the sparsity of the inverse covariance (concentration) matrix and allow for improved covariance estimation with lower computational complexity. We consider concentration estimation with the mean-squared error (MSE) as the objective, in a special type of model known as decomposable. This model includes, for example, the well known banded structure and other cases encountered in practice. Our first contribution is the derivation and analysis of the minimum variance unbiased estimator (MVUE) in decomposable graphical models. We provide a simple closed form solution to the MVUE and compare it with the classical maximum likelihood estimator (MLE) in terms of performance and complexity. Next, we extend the celebrated Stein's unbiased risk estimate (SURE) to graphical models. Using SURE, we prove that the MSE of the MVUE is always smaller or equal to that of the biased MLE, and that the MVUE itself is dominated by other approaches. In addition, we propose the use of SURE as a constructive mechanism for deriving new covariance estimators. Similarly to the classical MLE, all of our proposed estimators have simple closed form solutions but result in a significant reduction in MSE.

math.ST↗

arXiv2008

An Information Geometric Framework for Dimensionality Reduction

This report concerns the problem of dimensionality reduction through information geometric methods on statistical manifolds. While there has been considerable work recently presented regarding dimensionality reduction for the purposes of learning tasks such as classification, clustering, and visualization, these methods have focused primarily on Riemannian manifolds in Euclidean space. While sufficient for many applications, there are many high-dimensional signals which have no straightforward and meaningful Euclidean representation. In these cases, signals may be more appropriately represented as a realization of some distribution lying on a statistical manifold, or a manifold of probability density functions (PDFs). We present a framework for dimensionality reduction that uses information geometry for both statistical manifold reconstruction as well as dimensionality reduction in the data domain.

stat.ML↗

arXiv2008

Sparse image reconstruction for molecular imaging

The application that motivates this paper is molecular imaging at the atomic level. When discretized at sub-atomic distances, the volume is inherently sparse. Noiseless measurements from an imaging technology can be modeled by convolution of the image with the system point spread function (psf). Such is the case with magnetic resonance force microscopy (MRFM), an emerging technology where imaging of an individual tobacco mosaic virus was recently demonstrated with nanometer resolution. We also consider additive white Gaussian noise (AWGN) in the measurements. Many prior works of sparse estimators have focused on the case when H has low coherence; however, the system matrix H in our application is the convolution matrix for the system psf. A typical convolution matrix has high coherence. The paper therefore does not assume a low coherence H. A discrete-continuous form of the Laplacian and atom at zero (LAZE) p.d.f. used by Johnstone and Silverman is formulated, and two sparse estimators derived by maximizing the joint p.d.f. of the observation and image conditioned on the hyperparameters. A thresholding rule that generalizes the hard and soft thresholding rule appears in the course of the derivation. This so-called hybrid thresholding rule, when used in the iterative thresholding framework, gives rise to the hybrid estimator, a generalization of the lasso. Unbiased estimates of the hyperparameters for the lasso and hybrid estimator are obtained via Stein's unbiased risk estimate (SURE). A numerical study with a Gaussian psf and two sparse images shows that the hybrid estimator outperforms the lasso.

physics.data-an↗

arXiv2008

Decomposable Principal Component Analysis

We consider principal component analysis (PCA) in decomposable Gaussian graphical models. We exploit the prior information in these models in order to distribute its computation. For this purpose, we reformulate the problem in the sparse inverse covariance (concentration) domain and solve the global eigenvalue problem using a sequence of local eigenvalue problems in each of the cliques of the decomposable graph. We demonstrate the application of our methodology in the context of decentralized anomaly detection in the Abilene backbone network. Based on the topology of the network, we propose an approximate statistical graphical model and distribute the computation of PCA.

stat.ML↗

arXiv2008

Information Preserving Component Analysis: Data Projections for Flow Cytometry Analysis

Flow cytometry is often used to characterize the malignant cells in leukemia and lymphoma patients, traced to the level of the individual cell. Typically, flow cytometric data analysis is performed through a series of 2-dimensional projections onto the axes of the data set. Through the years, clinicians have determined combinations of different fluorescent markers which generate relatively known expression patterns for specific subtypes of leukemia and lymphoma -- cancers of the hematopoietic system. By only viewing a series of 2-dimensional projections, the high-dimensional nature of the data is rarely exploited. In this paper we present a means of determining a low-dimensional projection which maintains the high-dimensional relationships (i.e. information) between differing oncological data sets. By using machine learning techniques, we allow clinicians to visualize data in a low dimension defined by a linear combination of all of the available markers, rather than just 2 at a time. This provides an aid in diagnosing similar forms of cancer, as well as a means for variable selection in exploratory flow cytometric research. We refer to our method as Information Preserving Component Analysis (IPCA).

stat.ML↗

arXiv2008

Understanding Distal Transcriptional Regulation from Sequence Motif, Network Inference and Interactome Perspectives

Gene regulation in higher eukaryotes involves a complex interplay between the gene proximal promoter and distal genomic elements (such as enhancers) which work in concert to drive spatio-temporal expression. The experimental characterization of gene regulatory elements is a very complex and resource-intensive process. One of the major goals in computational biology is the \textit{in-silico} annotation of previously uncharacterized elements using results from the subset of known, annotated, regulatory elements. The computational annotation of these hitherto uncharacterized regions would require an identification of features that have good predictive value for regulatory behavior. In this work, we study transcriptional regulation as a problem in heterogeneous data integration, across sequence, expression and interactome level attributes. Using the example of the \textit{Gata2} gene and its recently discovered urogenital enhancers \cite{Khandekar2004} as a case study, we examine the predictive value of various high throughput functional genomic assays in characterizing these enhancers and their regulatory role. Observing results from the application of modern statistical learning methodologies for each of these data modalities, we propose a set of attributes that are most discriminatory in the localization and behavior of these enhancers.

q-bio.GN↗

arXiv2008

Classification Constrained Dimensionality Reduction

Dimensionality reduction is a topic of recent interest. In this paper, we present the classification constrained dimensionality reduction (CCDR) algorithm to account for label information. The algorithm can account for multiple classes as well as the semi-supervised setting. We present an out-of-sample expressions for both labeled and unlabeled data. For unlabeled data, we introduce a method of embedding a new point as preprocessing to a classifier. For labeled data, we introduce a method that improves the embedding during the training phase using the out-of-sample extension. We investigate classification performance using the CCDR algorithm on hyper-spectral satellite imagery data. We demonstrate the performance gain for both local and global classifiers and demonstrate a 10% improvement of the $k$-nearest neighbors algorithm performance. We present a connection between intrinsic dimension estimation and the optimal embedding dimension obtained using the CCDR algorithm.

stat.ML↗

arXiv2008

A greedy approach to sparse canonical correlation analysis

We consider the problem of sparse canonical correlation analysis (CCA), i.e., the search for two linear combinations, one for each multivariate, that yield maximum correlation using a specified number of variables. We propose an efficient numerical approximation based on a direct greedy approach which bounds the correlation at each stage. The method is specifically designed to cope with large data sets and its computational complexity depends only on the sparsity levels. We analyze the algorithm's performance through the tradeoff between correlation and parsimony. The results of numerical simulation suggest that a significant portion of the correlation may be captured using a relatively small number of variables. In addition, we examine the use of sparse CCA as a regularization method when the number of available samples is small compared to the dimensions of the multivariates.

stat.CO↗

arXiv2007

Finding Sequence Features in Tissue-specific Sequences

The discovery of motifs underlying gene expression is a challenging one. Some of these motifs are known transcription factors, but sequence inspection often provides valuable clues, even discovery of novel motifs with uncharacterized function in gene expression. Coupled with the complexity underlying tissue-specific gene expression, there are several motifs that are putatively responsible for expression in a certain cell type. This has important implications in understanding fundamental biological processes, such as development and disease progression. In this work, we present an approach to the principled selection of motifs (not necessarily transcription factor sites) and examine its application to several questions in current bioinformatics research. There are two main contributions of this work: Firstly, we introduce a new metric for variable selection during classification, and secondly, we investigate a problem of finding specific sequence motifs that underlie tissue specific gene expression. In conjunction with the SVM classifier we find these motifs and discover several novel motifs which have not yet been attributed with any particular functional role (eg: TFBS binding motifs). We hypothesize that the discovery of these motifs would enable the large-scale investigation for the tissue specific regulatory potential of any conserved sequence element identified from genome-wide studies. Finally, we propose the utility of this developed framework to not only aid discovery of discriminatory motifs, but also to examine the role of any motif of choice in co-regulation or co-expression of gene groups.

q-bio.GN↗