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<p>With the advance of technology, the collection and storage of data has become routine. Huge amount of data are increasingly produced from biological experiments. the advent of DNA microarray technologies has enabled scientists to measure expressions of tens of thousands of genes simultaneously. Single nucleotide polymorphism (SNP) are being used in genetic association with a wide range of phenotypes, for example, complex diseases. These high-dimensional problems are becoming more and more common. The "large p, small n" problem, in which there are more variables than samples, currently a challenge that many statisticians face. The penalized variable selection method is an effective method to deal with "large p, small n" problem. In particular, The Lasso (least absolute selection and shrinkage operator) proposed by Tibshirani has become an effective method to deal with this type of problem. the Lasso works well for the covariates which can be treated individually. When the covariates are grouped, it does not work well. Elastic net, group lasso, group MCP and group bridge are extensions of the Lasso. Group lasso enforces sparsity at the group level, rather than at the level of the individual covariates. Group bridge, group MCP produces sparse solutions both at the group level and at the level of the individual covariates within a group. Our simulation study shows that the group lasso forces complete grouping, group MCP encourages grouping to a rather slight extent, and group bridge is somewhere in between. If one expects that the proportion of nonzero group members to be greater than one-half, group lasso maybe a good choice; otherwise group MCP would be preferred. If one expects this proportion to be close to one-half, one may wish to use group bridge. A real data analysis example is also conducted for genetic variation (SNPs) data to find out the associations between SNPs and West Nile disease.</p> / Master of Science (MSc)

One of the major goals in large-scale genomic studies is to identify genes with a prognostic impact on time-to-event outcomes, providing insight into the disease's process. With the rapid developments in high-throughput genomic technologies in the past two decades, the scientific community is able to monitor the expression levels of thousands of genes and proteins resulting in enormous data sets where the number of genomic variables (covariates) is far greater than the number of subjects. It is also typical for such data sets to have a high proportion of censored observations. Methods based on univariate Cox regression are often used to select genes related to survival outcome. However, the Cox model assumes proportional hazards (PH), which is unlikely to hold for each gene. When applied to genes exhibiting some form of non-proportional hazards (NPH), these methods could lead to an under- or over-estimation of the effects. In this thesis, we develop methods that will directly address t / Statistics

With the rapid development of modern high-throughput technologies, scientists can now collect high-dimensional complex data in different forms, such as medical images, genomics measurements. However, acquisition of more data does not automatically lead to better knowledge discovery. One needs efficient and reliable analytical tools to extract useful information from complex datasets. The main objective of this dissertation is to develop innovative Bayesian methodologies to enable effective and efficient knowledge discovery from complex high-dimensional data. It contains two parts—the development of computationally efficient functional mixed models and the modeling of data heterogeneity via Dirichlet Diffusion Tree. The first part focuses on tackling the computational bottleneck in Bayesian functional mixed models. We propose a computational framework called variational functional mixed model (VFMM). This new method facilitates efficient data compression and high-performance computing in basis space. We also propose a new multiple testing procedure in basis space, which can be used to detect significant local regions. The effectiveness of the proposed model is demonstrated through two datasets, a mass spectrometry dataset in a cancer study and a neuroimaging dataset in an Alzheimer's disease study. The second part is about modeling data heterogeneity by using Dirichlet Diffusion Trees. We propose a Bayesian latent tree model that incorporates covariates of subjects to characterize the heterogeneity and uncover the latent tree structure underlying data. This innovative model may reveal the hierarchical evolution process through branch structures and estimate systematic differences between groups of samples. We demonstrate the effectiveness of the model through the simulation study and a brain tumor real data. / Doctor of Philosophy / With the rapid development of modern high-throughput technologies, scientists can now collect high-dimensional data in different forms, such as engineering signals, medical images, and genomics measurements. However, acquisition of such data does not automatically lead to efficient knowledge discovery. The main objective of this dissertation is to develop novel Bayesian methods to extract useful knowledge from complex high-dimensional data. It has two parts—the development of an ultra-fast functional mixed model and the modeling of data heterogeneity via Dirichlet Diffusion Trees. The first part focuses on developing approximate Bayesian methods in functional mixed models to estimate parameters and detect significant regions. Two datasets demonstrate the effectiveness of proposed method—a mass spectrometry dataset in a cancer study and a neuroimaging dataset in an Alzheimer's disease study. The second part focuses on modeling data heterogeneity via Dirichlet Diffusion Trees. The method helps uncover the underlying hierarchical tree structures and estimate systematic differences between the group of samples. We demonstrate the effectiveness of the method through the brain tumor imaging data.