| Literature DB >> 16306880 |
Martin Moorhead1, Paul Hardenbol, Farooq Siddiqui, Matthew Falkowski, Carsten Bruckner, James Ireland, Hywel B Jones, Maneesh Jain, Thomas D Willis, Malek Faham.
Abstract
High-throughput genotyping technologies that enable large association studies are already available. Tools for genotype determination starting from raw signal intensities need to be automated, robust, and flexible to provide optimal genotype determination given the specific requirements of a study. The key metrics describing the performance of a custom genotyping study are assay conversion, call rate, and genotype accuracy. These three metrics can be traded off against each other. Using the highly multiplexed Molecular Inversion Probe technology as an example, we describe a methodology for identifying the optimal trade-off. The methodology comprises: a robust clustering algorithm and assessment of a large number of data filter sets. The clustering algorithm allows for automatic genotype determination. Many different sets of filters are then applied to the clustered data, and performance metrics resulting from each filter set are calculated. These performance metrics relate to the power of a study and provide a framework to choose the most suitable filter set to the particular study.Mesh:
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Year: 2006 PMID: 16306880 DOI: 10.1038/sj.ejhg.5201528
Source DB: PubMed Journal: Eur J Hum Genet ISSN: 1018-4813 Impact factor: 4.246