Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Block-Diagonal Constrained Low-Rank and Sparse Graph for Discriminant Analysis of Image Data.

ABSTRACT: Recently, low-rank and sparse model-based dimensionality reduction (DR) methods have aroused lots of interest. In this paper, we propose an effective supervised DR technique named block-diagonal constrained low-rank and sparse-based embedding (BLSE). BLSE has two steps, i.e., block-diagonal constrained low-rank and sparse representation (BLSR) and block-diagonal constrained low-rank and sparse graph embedding (BLSGE). Firstly, the BLSR model is developed to reveal the intrinsic intra-class and inter-class adjacent relationships as well as the local neighborhood relations and global structure of data. Particularly, there are mainly three items considered in BLSR. First, a sparse constraint is required to discover the local data structure. Second, a low-rank criterion is incorporated to capture the global structure in data. Third, a block-diagonal regularization is imposed on the representation to promote discrimination between different classes. Based on BLSR, informative and discriminative intra-class and inter-class graphs are constructed. With the graphs, BLSGE seeks a low-dimensional embedding subspace by simultaneously minimizing the intra-class scatter and maximizing the inter-class scatter. Experiments on public benchmark face and object image datasets demonstrate the effectiveness of the proposed approach.

SUBMITTER: Guo T

PROVIDER: S-EPMC5539604 | biostudies-other | 2017 Jun

REPOSITORIES: biostudies-other

ACCESS DATA

Json Xml

Similar Datasets

Unmixing biological fluorescence image data with sparse and low-rank Poisson regression.

Project description:MotivationMultispectral biological fluorescence microscopy has enabled the identification of multiple targets in complex samples. The accuracy in the unmixing result degrades (i) as the number of fluorophores used in any experiment increases and (ii) as the signal-to-noise ratio in the recorded images decreases. Further, the availability of prior knowledge regarding the expected spatial distributions of fluorophores in images of labeled cells provides an opportunity to improve the accuracy of fluorophore identification and abundance.ResultsWe propose a regularized sparse and low-rank Poisson regression unmixing approach (SL-PRU) to deconvolve spectral images labeled with highly overlapping fluorophores which are recorded in low signal-to-noise regimes. First, SL-PRU implements multipenalty terms when pursuing sparseness and spatial correlation of the resulting abundances in small neighborhoods simultaneously. Second, SL-PRU makes use of Poisson regression for unmixing instead of least squares regression to better estimate photon abundance. Third, we propose a method to tune the SL-PRU parameters involved in the unmixing procedure in the absence of knowledge of the ground truth abundance information in a recorded image. By validating on simulated and real-world images, we show that our proposed method leads to improved accuracy in unmixing fluorophores with highly overlapping spectra.Availability and implementationThe source code used for this article was written in MATLAB and is available with the test data at https://github.com/WANGRUOGU/SL-PRU.

| S-EPMC10081874 | biostudies-literature

Block-diagonal discriminant analysis and its bias-corrected rules.

Project description:High-throughput expression profiling allows simultaneous measure of tens of thousands of genes at once. These data have motivated the development of reliable biomarkers for disease subtypes identification and diagnosis. Many methods have been developed in the literature for analyzing these data, such as diagonal discriminant analysis, support vector machines, and k-nearest neighbor methods. The diagonal discriminant methods have been shown to perform well for high-dimensional data with small sample sizes. Despite its popularity, the independence assumption is unlikely to be true in practice. Recently, a gene module based linear discriminant analysis strategy has been proposed by utilizing the correlation among genes in discriminant analysis. However, the approach can be underpowered when the samples of the two classes are unbalanced. In this paper, we propose to correct the biases in the discriminant scores of block-diagonal discriminant analysis. In simulation studies, our proposed method outperforms other approaches in various settings. We also illustrate our proposed discriminant analysis method for analyzing microarray data studies.

| S-EPMC3856189 | biostudies-literature

Low-Rank Graph-Regularized Structured Sparse Regression for Identifying Genetic Biomarkers.

Project description:In this paper, we propose a novel sparse regression method for Brain-Wide and Genome-Wide association study. Specifically, we impose a low-rank constraint on the weight coefficient matrix and then decompose it into two low-rank matrices, which find relationships in genetic features and in brain imaging features, respectively. We also introduce a sparse acyclic digraph with sparsity-inducing penalty to take further into account the correlations among the genetic variables, by which it can be possible to identify the representative SNPs that are highly associated with the brain imaging features. We optimize our objective function by jointly tackling low-rank regression and variable selection in a framework. In our method, the low-rank constraint allows us to conduct variable selection with the low-rank representations of the data; the learned low-sparsity weight coefficients allow discarding unimportant variables at the end. The experimental results on the Alzheimer's Disease Neuroimaging Initiative (ADNI) dataset showed that the proposed method could select the important SNPs to more accurately estimate the brain imaging features than the state-of-the-art methods.

| S-EPMC5929142 | biostudies-literature

Low-Rank and Sparse Recovery of Human Gait Data.

Project description:Due to occlusion or detached markers, information can often be lost while capturing human motion with optical tracking systems. Based on three natural properties of human gait movement, this study presents two different approaches to recover corrupted motion data. These properties are used to define a reconstruction model combining low-rank matrix completion of the measured data with a group-sparsity prior on the marker trajectories mapped in the frequency domain. Unlike most existing approaches, the proposed methodology is fully unsupervised and does not need training data or kinematic information of the user. We evaluated our methods on four different gait datasets with various gap lengths and compared their performance with a state-of-the-art approach using principal component analysis (PCA). Our results showed recovering missing data more precisely, with a reduction of at least 2 mm in mean reconstruction error compared to the literature method. When a small number of marker trajectories is available, our findings showed a reduction of more than 14 mm for the mean reconstruction error compared to the literature approach.

| S-EPMC7472490 | biostudies-literature

Low-Rank and Sparse Matrix Decomposition for Genetic Interaction Data.

Project description:BackgroundEpistatic miniarray profile (EMAP) studies have enabled the mapping of large-scale genetic interaction networks and generated large amounts of data in model organisms. One approach to analyze EMAP data is to identify gene modules with densely interacting genes. In addition, genetic interaction score (S score) reflects the degree of synergizing or mitigating effect of two mutants, which is also informative. Statistical approaches that exploit both modularity and the pairwise interactions may provide more insight into the underlying biology. However, the high missing rate in EMAP data hinders the development of such approaches. To address the above problem, we adopted the matrix decomposition methodology "low-rank and sparse decomposition" (LRSDec) to decompose EMAP data matrix into low-rank part and sparse part.ResultsLRSDec has been demonstrated as an effective technique for analyzing EMAP data. We applied a synthetic dataset and an EMAP dataset studying RNA-related processes in Saccharomyces cerevisiae. Global views of the genetic cross talk between different RNA-related protein complexes and processes have been structured, and novel functions of genes have been predicted.

| S-EPMC4529927 | biostudies-literature

Sparse low-rank separated representation models for learning from data.

Project description:We consider the problem of learning a multivariate function from a set of scattered observations using a sparse low-rank separated representation (SSR) model. The model structure considered here is promising for high-dimensional learning problems; however, existing training algorithms based on alternating least-squares (ALS) are known to have convergence difficulties, particularly when the rank of the model is greater than 1. In the present work, we supplement the model structure with sparsity constraints to ensure the well posedness of the approximation problem. We propose two fast training algorithms to estimate the model parameters: (i) a cyclic coordinate descent algorithm and (ii) a block coordinate descent (BCD) algorithm. While the first algorithm is not provably convergent owing to the non-convexity of the optimization problem, the BCD algorithm guarantees convergence to a Nash equilibrium point. The computational cost of the proposed algorithms is shown to scale linearly with respect to all of the parameters in contrast to methods based on ALS. Numerical studies on synthetic and real-world regression datasets indicate that the proposed SSR model structure holds significant potential for machine learning problems.

| S-EPMC6364613 | biostudies-literature

Beyond Low Rank + Sparse: Multi-scale Low Rank Matrix Decomposition.

Project description:We present a natural generalization of the recent low rank + sparse matrix decomposition and consider the decomposition of matrices into components of multiple scales. Such decomposition is well motivated in practice as data matrices often exhibit local correlations in multiple scales. Concretely, we propose a multi-scale low rank modeling that represents a data matrix as a sum of block-wise low rank matrices with increasing scales of block sizes. We then consider the inverse problem of decomposing the data matrix into its multi-scale low rank components and approach the problem via a convex formulation. Theoretically, we show that under various incoherence conditions, the convex program recovers the multi-scale low rank components either exactly or approximately. Practically, we provide guidance on selecting the regularization parameters and incorporate cycle spinning to reduce blocking artifacts. Experimentally, we show that the multi-scale low rank decomposition provides a more intuitive decomposition than conventional low rank methods and demonstrate its effectiveness in four applications, including illumination normalization for face images, motion separation for surveillance videos, multi-scale modeling of the dynamic contrast enhanced magnetic resonance imaging and collaborative filtering exploiting age information.

| S-EPMC5403160 | biostudies-literature

Shrinkage-based diagonal discriminant analysis and its applications in high-dimensional data.

Project description:High-dimensional data such as microarrays have brought us new statistical challenges. For example, using a large number of genes to classify samples based on a small number of microarrays remains a difficult problem. Diagonal discriminant analysis, support vector machines, and k-nearest neighbor have been suggested as among the best methods for small sample size situations, but none was found to be superior to others. In this article, we propose an improved diagonal discriminant approach through shrinkage and regularization of the variances. The performance of our new approach along with the existing methods is studied through simulations and applications to real data. These studies show that the proposed shrinkage-based and regularization diagonal discriminant methods have lower misclassification rates than existing methods in many cases.

| S-EPMC2794982 | biostudies-literature

Sparse linear discriminant analysis for multiview structured data.

Project description:Classification methods that leverage the strengths of data from multiple sources (multiview data) simultaneously have enormous potential to yield more powerful findings than two-step methods: association followed by classification. We propose two methods, sparse integrative discriminant analysis (SIDA), and SIDA with incorporation of network information (SIDANet), for joint association and classification studies. The methods consider the overall association between multiview data, and the separation within each view in choosing discriminant vectors that are associated and optimally separate subjects into different classes. SIDANet is among the first methods to incorporate prior structural information in joint association and classification studies. It uses the normalized Laplacian of a graph to smooth coefficients of predictor variables, thus encouraging selection of predictors that are connected. We demonstrate the effectiveness of our methods on a set of synthetic datasets and explore their use in identifying potential nontraditional risk factors that discriminate healthy patients at low versus high risk for developing atherosclerosis cardiovascular disease in 10 years. Our findings underscore the benefit of joint association and classification methods if the goal is to correlate multiview data and to perform classification.

| S-EPMC8906173 | biostudies-literature

Sparse Linear Discriminant Analysis using the Prior-Knowledge-Guided Block Covariance Matrix.

Project description:There are two key challenges when using a linear discriminant analysis in the high-dimensional setting, including singularity of the covariance matrix and difficulty of interpreting the resulting classifier. Although several methods have been proposed to address these problems, they focused only on identifying a parsimonious set of variables maximizing classification accuracy. However, most methods did not consider dependency between variables and efficacy of selected variables appropriately. To address these limitations, here we propose a new approach that directly estimates the sparse discriminant vector without a need of estimating the whole inverse covariance matrix, by formulating a quadratic optimization problem. Furthermore, this approach also allows to integrate external information to guide the structure of covariance matrix. We evaluated the proposed model with simulation studies. We then applied it to the transcriptomic study that aims to identify genomic markers predictive of the response to cancer immunotherapy, where the covariance matrix was constructed based on the prior knowledge available in the pathway database.

| S-EPMC7505231 | biostudies-literature

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data