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  Experimental design for genome-wide association studies

Lippert, C., Stegle, O., Nickisch, H., Borgwardt, K., & Weigel, D. (2010). Experimental design for genome-wide association studies. Poster presented at 18th Annual International Conference on Intelligent Systems for Molecular Biology (ISMB 2010), Boston, MA, USA.

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 Creators:
Lippert, C1, 2, Author           
Stegle, O1, 2, Author           
Nickisch, H1, 3, Author           
Borgwardt, KM1, 2, Author           
Weigel, D4, Author
Affiliations:
1Max Planck Institute for Biological Cybernetics, Max Planck Society, ou_1497794              
2Former Research Group Machine Learning and Computational Biology, Max Planck Institute for Biological Cybernetics, Max Planck Society, ou_2528696              
3Department Empirical Inference, Max Planck Institute for Biological Cybernetics, Max Planck Society, ou_1497795              
4Max Planck Institute for Developmental Biology, Max Planck Society, Max-Planck-Ring 5, 72076 Tübingen, DE, ou_2421691              

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 Abstract: Background / Purpose:
Genetic association studies have become an integral tool to understand how genetic variation effects a growing selection of phenotypes. These may range from molecular phenotypes, such as gene expression, to global phenotypes such as growth rate or floweringtime of plants. Thanks to recent advances in sequencing technology, large-scale genotype information for hundreds, soon thousands of humans, plants and animals are now available or soon to be released. If new phenotypes are being studied, it is rarely feasible to phenotype all the individuals, due to cost and or time constraints. To solve this emerging problem of appropriate sample selection we propose and investigate experimental design by a principled information criterion.
Main conclusion:
In a retrospective real-data study on a flowering-time QTL study of 166 individuals of A. thaliana (Atwell et al 2010), we demonstrate the viability of experimental design in genome-wide association studies, achieving a significant improvement over a non-optimised study layout and simple baseline selection criteria. (See figure on poster: “RMSE on independent test set”: Experimental design curves for the Bayesian Lasso and various selection criteria compared to random selection on the A. thaliana flowering-time dataset. ALC denotes the area under the learning curve.)
Disclosures:
No relevant conflicts of interest declared.

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 Dates: 2010-07
 Publication Status: Issued
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Title: 18th Annual International Conference on Intelligent Systems for Molecular Biology (ISMB 2010)
Place of Event: Boston, MA, USA
Start-/End Date: 2010-07-17 - 2010-07-19

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Title: F1000Posters
Source Genre: Proceedings
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Pages: - Volume / Issue: 2010 (1) Sequence Number: - Start / End Page: 324 Identifier: -