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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