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Using LASSO regression to detect predictive aggregate effects in genetic studies

We use least absolute shrinkage and selection operator (LASSO) regression to select genetic markers and phenotypic features that are most informative with respect to a trait of interest. We compare several strategies for applying LASSO methods in risk prediction models, using the Genetic Analysis Wo...

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Detalles Bibliográficos
Autores principales: Fontanarosa, Joel B, Dai, Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287908/
https://www.ncbi.nlm.nih.gov/pubmed/22373537
http://dx.doi.org/10.1186/1753-6561-5-S9-S69
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author Fontanarosa, Joel B
Dai, Yang
author_facet Fontanarosa, Joel B
Dai, Yang
author_sort Fontanarosa, Joel B
collection PubMed
description We use least absolute shrinkage and selection operator (LASSO) regression to select genetic markers and phenotypic features that are most informative with respect to a trait of interest. We compare several strategies for applying LASSO methods in risk prediction models, using the Genetic Analysis Workshop 17 exome simulation data consisting of 697 individuals with information on genotypic and phenotypic features (smoking, age, sex) in 5-fold cross-validated fashion. The cross-validated averages of the area under the receiver operating curve range from 0.45 to 0.63 for different strategies using only genotypic markers. The same values are improved to 0.69–0.87 when both genotypic and phenotypic information are used. The ability of the LASSO method to find true causal markers is limited, but the method was able to discover several common variants (e.g., FLT1) under certain conditions.
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spelling pubmed-32879082012-02-28 Using LASSO regression to detect predictive aggregate effects in genetic studies Fontanarosa, Joel B Dai, Yang BMC Proc Proceedings We use least absolute shrinkage and selection operator (LASSO) regression to select genetic markers and phenotypic features that are most informative with respect to a trait of interest. We compare several strategies for applying LASSO methods in risk prediction models, using the Genetic Analysis Workshop 17 exome simulation data consisting of 697 individuals with information on genotypic and phenotypic features (smoking, age, sex) in 5-fold cross-validated fashion. The cross-validated averages of the area under the receiver operating curve range from 0.45 to 0.63 for different strategies using only genotypic markers. The same values are improved to 0.69–0.87 when both genotypic and phenotypic information are used. The ability of the LASSO method to find true causal markers is limited, but the method was able to discover several common variants (e.g., FLT1) under certain conditions. BioMed Central 2011-11-29 /pmc/articles/PMC3287908/ /pubmed/22373537 http://dx.doi.org/10.1186/1753-6561-5-S9-S69 Text en Copyright ©2011 Fontanarosa and Dai; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Proceedings
Fontanarosa, Joel B
Dai, Yang
Using LASSO regression to detect predictive aggregate effects in genetic studies
title Using LASSO regression to detect predictive aggregate effects in genetic studies
title_full Using LASSO regression to detect predictive aggregate effects in genetic studies
title_fullStr Using LASSO regression to detect predictive aggregate effects in genetic studies
title_full_unstemmed Using LASSO regression to detect predictive aggregate effects in genetic studies
title_short Using LASSO regression to detect predictive aggregate effects in genetic studies
title_sort using lasso regression to detect predictive aggregate effects in genetic studies
topic Proceedings
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287908/
https://www.ncbi.nlm.nih.gov/pubmed/22373537
http://dx.doi.org/10.1186/1753-6561-5-S9-S69
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