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For data with high-dimensional covariates but small to moderate sample sizes, the analysis of single datasets often generates unsatisfactory results. The integrative analysis of multiple independent datasets provides an effective way of pooling infor mation and outperforms single-dataset analysis and some alternative multi-datasets approaches including meta-analysis. Under certain scenarios, multiple datasets are expected to share common important covariates, that is, the multiple models have similarity in sparsity structures. However, the existing methods do not have a mechanism to {it promote} the similarity of sparsity structures in integrative analysis. In this study, we consider penalized variable selection and estimation in integrative analysis. We develop an $L_0$-penalty based approach, which is the first to explicitly promote the similarity of sparsity structures. Computationally it is realized using a coordinate descent algorithm. Theoretically it has the much desired consistency properties. In simulation, it significantly outperforms the competing alternative when the models in multiple datasets share common important covariates. It has better or similar performance as the alternative when the sparsity structures share no similarity. Thus it provides a safe choice for data analysis. Applying the proposed method to three lung cancer datasets with gene expression measurements leads to models with significantly more similar sparsity structures and better prediction performance.
For survival data with high-dimensional covariates, results generated in the analysis of a single dataset are often unsatisfactory because of the small sample size. Integrative analysis pools raw data from multiple independent studies with comparable designs, effectively increases sample size, and has better performance than meta-analysis and single-dataset analysis. In this study, we conduct integrative analysis of survival data under the accelerated failure time (AFT) model. The sparsity structures of multiple datasets are described using the homogeneity and heterogeneity models. For variable selection under the homogeneity model, we adopt group penalization approaches. For variable selection under the heterogeneity model, we use composite penalization and sparse group penalization approaches. As a major advancement from the existing studies, the asymptotic selection and estimation properties are rigorously established. Simulation study is conducted to compare different penalization methods and against alternatives. We also analyze four lung cancer prognosis datasets with gene expression measurements.
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