Do you want to publish a course? Click here

Improved Inference of Gaussian Mixture Copula Model for Clustering and Reproducibility Analysis using Automatic Differentiation

155   0   0.0 ( 0 )
 Added by Siva Rajesh Kasa
 Publication date 2020
and research's language is English




Ask ChatGPT about the research

Copulas provide a modular parameterization of multivariate distributions that decouples the modeling of marginals from the dependencies between them. Gaussian Mixture Copula Model (GMCM) is a highly flexible copula that can model many kinds of multi-modal dependencies, as well as asymmetric and tail dependencies. They have been effectively used in clustering non-Gaussian data and in Reproducibility Analysis, a meta-analysis method designed to verify the reliability and consistency of multiple high-throughput experiments. Parameter estimation for GMCM is challenging due to its intractable likelihood. The best previous methods have maximized a proxy-likelihood through a Pseudo Expectation Maximization (PEM) algorithm. They have no guarantees of convergence or convergence to the correct parameters. In this paper, we use Automatic Differentiation (AD) tools to develop a method, called AD-GMCM, that can maximize the exact GMCM likelihood. In our simulation studies and experiments with real data, AD-GMCM finds more accurate parameter estimates than PEM and yields better performance in clustering and Reproducibility Analysis. We discuss the advantages of an AD-based approach, to address problems related to monotonic increase of likelihood and parameter identifiability in GMCM. We also analyze, for GMCM, two well-known cases of degeneracy of maximum likelihood in GMM that can lead to spurious clustering solutions. Our analysis shows that, unlike GMM, GMCM is not affected in one of the cases.



rate research

Read More

We consider clustering based on significance tests for Gaussian Mixture Models (GMMs). Our starting point is the SigClust method developed by Liu et al. (2008), which introduces a test based on the k-means objective (with k = 2) to decide whether the data should be split into two clusters. When applied recursively, this test yields a method for hierarchical clustering that is equipped with a significance guarantee. We study the limiting distribution and power of this approach in some examples and show that there are large regions of the parameter space where the power is low. We then introduce a new test based on the idea of relative fit. Unlike prior work, we test for whether a mixture of Gaussians provides a better fit relative to a single Gaussian, without assuming that either model is correct. The proposed test has a simple critical value and provides provable error control. One version of our test provides exact, finite sample control of the type I error. We show how our tests can be used for hierarchical clustering as well as in a sequential manner for model selection. We conclude with an extensive simulation study and a cluster analysis of a gene expression dataset.
In recent biomedical scientific problems, it is a fundamental issue to integratively cluster a set of objects from multiple sources of datasets. Such problems are mostly encountered in genomics, where data is collected from various sources, and typically represent distinct yet complementary information. Integrating these data sources for multi-source clustering is challenging due to their complex dependence structure including directional dependency. Particularly in genomics studies, it is known that there is certain directional dependence between DNA expression, DNA methylation, and RNA expression, widely called The Central Dogma. Most of the existing multi-view clustering methods either assume an independent structure or pair-wise (non-directional) dependency, thereby ignoring the directional relationship. Motivated by this, we propose a copula-based multi-view clustering model where a copula enables the model to accommodate the directional dependence existing in the datasets. We conduct a simulation experiment where the simulated datasets exhibiting inherent directional dependence: it turns out that ignoring the directional dependence negatively affects the clustering performance. As a real application, we applied our model to the breast cancer tumor samples collected from The Cancer Genome Altas (TCGA).
Poverty is a multidimensional concept often comprising a monetary outcome and other welfare dimensions such as education, subjective well-being or health, that are measured on an ordinal scale. In applied research, multidimensional poverty is ubiquitously assessed by studying each poverty dimension independently in univariate regression models or by combining several poverty dimensions into a scalar index. This inhibits a thorough analysis of the potentially varying interdependence between the poverty dimensions. We propose a multivariate copula generalized additive model for location, scale and shape (copula GAMLSS or distributional copula model) to tackle this challenge. By relating the copula parameter to covariates, we specifically examine if certain factors determine the dependence between poverty dimensions. Furthermore, specifying the full conditional bivariate distribution, allows us to derive several features such as poverty risks and dependence measures coherently from one model for different individuals. We demonstrate the approach by studying two important poverty dimensions: income and education. Since the level of education is measured on an ordinal scale while income is continuous, we extend the bivariate copula GAMLSS to the case of mixed ordered-continuous outcomes. The new model is integrated into the GJRM package in R and applied to data from Indonesia. Particular emphasis is given to the spatial variation of the income-education dependence and groups of individuals at risk of being simultaneously poor in both education and income dimensions.
In the genomic era, the identification of gene signatures associated with disease is of significant interest. Such signatures are often used to predict clinical outcomes in new patients and aid clinical decision-making. However, recent studies have shown that gene signatures are often not replicable. This occurrence has practical implications regarding the generalizability and clinical applicability of such signatures. To improve replicability, we introduce a novel approach to select gene signatures from multiple datasets whose effects are consistently non-zero and account for between-study heterogeneity. We build our model upon some rank-based quantities, facilitating integration over different genomic datasets. A high dimensional penalized Generalized Linear Mixed Model (pGLMM) is used to select gene signatures and address data heterogeneity. We compare our method to some commonly used strategies that select gene signatures ignoring between-study heterogeneity. We provide asymptotic results justifying the performance of our method and demonstrate its advantage in the presence of heterogeneity through thorough simulation studies. Lastly, we motivate our method through a case study subtyping pancreatic cancer patients from four gene expression studies.
In this paper, a Bayesian semiparametric copula approach is used to model the underlying multivariate distribution $F_{true}$. First, the Dirichlet process is constructed on the unknown marginal distributions of $F_{true}$. Then a Gaussian copula model is utilized to capture the dependence structure of $F_{true}$. As a result, a Bayesian multivariate normality test is developed by combining the relative belief ratio and the Energy distance. Several interesting theoretical results of the approach are derived. Finally, through several simulated examples and a real data set, the proposed approach reveals excellent performance.
comments
Fetching comments Fetching comments
Sign in to be able to follow your search criteria
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا