Abstract
A general method for regressing a continuous response upon large groups of diverse genetic covariates via dimension reduction is developed and exemplified. It is shown that allowing latent features derived from different covariate groups to interact aids in prediction when interactions subsist among the original covariates. A means of selecting a subset of relevant covariates from the original set is proposed, and a simulation study is performed to demonstrate the effectiveness of the procedure for prediction and variable selection. The procedure is applied to a high-dimensional lung cancer data set to model the effects of gene expression, copy number variation, and methylation on a drug response.
| Original language | English (US) |
|---|---|
| Title of host publication | Proceedings 2012 IEEE International Workshop on Genomic Signal Processing and Statistics, GENSIPS 2012 |
| Pages | 130-134 |
| Number of pages | 5 |
| DOIs | |
| State | Published - 2012 |
| Externally published | Yes |
| Event | 2012 IEEE International Workshop on Genomic Signal Processing and Statistics, GENSIPS 2012 - Washington, DC, United States Duration: Dec 2 2012 → Dec 4 2012 |
Publication series
| Name | Proceedings - IEEE International Workshop on Genomic Signal Processing and Statistics |
|---|---|
| ISSN (Print) | 2150-3001 |
| ISSN (Electronic) | 2150-301X |
Conference
| Conference | 2012 IEEE International Workshop on Genomic Signal Processing and Statistics, GENSIPS 2012 |
|---|---|
| Country/Territory | United States |
| City | Washington, DC |
| Period | 12/2/12 → 12/4/12 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
ASJC Scopus subject areas
- Biochemistry, Genetics and Molecular Biology (miscellaneous)
- Computational Theory and Mathematics
- Signal Processing
- Biomedical Engineering
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