||5R21CA157219-03 Interpret this number
||University Of Michigan
||Integrated Analysis of High Throughput Cancer Genomic Data
Project Summary and Relevance
The primary goal of this project is to develop a novel, integrated approach for the analysis of high-throughput cancer
genomic data. We plan to develop new variable selection methods for 1) class discovery, that is we propose to determine
subgroups of the specified cancer to better understand the underlying cancer biology and 2) predictive gene signatures,
that is we propose to determine a subset of genes which are predictive for patients' clinical phenotypes, including survival
and response to therapy.
Specifically, we will develop a new method for variable selection in clustering. Clustering plays a critical role in
the analysis of genomic cancer data. For example, based on the gene expression profiles, important cluster distinctions
can be found among a set of tissue samples, which may reflect categories of diseases, mutation status, or different
responses to a given therapy. Second, we will develop a new penalized-likelihood method for variable selection in
regression which utilizes group information to select groups of correlated genes that share the same biological pathway.
The developed methodology will be useful for identifying important gene signatures that may lead to more effective
personalized treatment in any health studies where survival time or response to therapy is of interest.
A semiparametrically efficient estimator of the time-varying effects for survival data with time-dependent treatment.
, Fei Z.
, Li Y.
Scandinavian Journal Of Statistics, Theory And Applications, 2016 Sep; 43(3), p. 649-663.
Selection of latent variables for multiple mixed-outcome models.
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Scandinavian Journal Of Statistics, Theory And Applications, 2014 Dec; 41(4), p. 1064-1082.
Discrete mixture modeling to address genetic heterogeneity in time-to-event regression.
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Ultrahigh dimensional time course feature selection.
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The Dantzig Selector for Censored Linear Regression Models.
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Statistica Sinica, 2014-01-01 00:00:00.0; 24(1), p. 251-2568.