Bioinformatics (Oxford, England) · 2009
Genome-wide association analysis by lasso penalized logistic regression.
СтатьяПоддержка NIH: внешняя программаНазвание и аннотация: Перевод пока не подготовлен
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Wu Tong Tong, Chen Yi Fang, Hastie Trevor, Sobel Eric, Lange Kenneth
Аннотация
MOTIVATION: In ordinary regression, imposition of a lasso penalty makes continuous model selection straightforward. Lasso penalized regression is particularly advantageous when the number of predictors far exceeds the number of observations.
METHOD: The present article evaluates the performance of lasso penalized logistic regression in case-control disease gene mapping with a large number of SNPs (single nucleotide polymorphisms) predictors. The strength of the lasso penalty can be tuned to select a predetermined number of the most relevant SNPs and other predictors. For a given value of the tuning constant, the penalized likelihood is quickly maximized by cyclic coordinate ascent. Once the most potent marginal predictors are identified, their two-way and higher order interactions can also be examined by lasso penalized logistic regression.
RESULTS: This strategy is tested on both simulated and real data. Our findings on coeliac disease replicate the previous SNP results and shed light on possible interactions among the SNPs.
AVAILABILITY: The software discussed is available in Mendel 9.0 at the UCLA Human Genetics web site.
SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
METHOD: The present article evaluates the performance of lasso penalized logistic regression in case-control disease gene mapping with a large number of SNPs (single nucleotide polymorphisms) predictors. The strength of the lasso penalty can be tuned to select a predetermined number of the most relevant SNPs and other predictors. For a given value of the tuning constant, the penalized likelihood is quickly maximized by cyclic coordinate ascent. Once the most potent marginal predictors are identified, their two-way and higher order interactions can also be examined by lasso penalized logistic regression.
RESULTS: This strategy is tested on both simulated and real data. Our findings on coeliac disease replicate the previous SNP results and shed light on possible interactions among the SNPs.
AVAILABILITY: The software discussed is available in Mendel 9.0 at the UCLA Human Genetics web site.
SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.