Highly multiplexed molecular inversion probe genotyping: Over 10,000 targeted SNPs genotyped in a single tube assay

Paul Hardenbol(Trellis Bioscience (United States)), Fuli Yu(Baylor College of Medicine), John W. Belmont(Baylor College of Medicine), Jennifer MacKenzie(Assembly Biosciences (United States)), Carsten Bruckner(Assembly Biosciences (United States)), Tiffany Brundage(Assembly Biosciences (United States)), Andrew Boudreau(Assembly Biosciences (United States)), Steve Chow(Assembly Biosciences (United States)), Jim Eberle(Assembly Biosciences (United States)), Ayça Erbilgin(Assembly Biosciences (United States)), Mat Falkowski(Assembly Biosciences (United States)), R.C. Fitzgerald(Assembly Biosciences (United States)), Sy Ghose(Baylor College of Medicine), Oleg Iartchouk(Assembly Biosciences (United States)), Maneesh Jain(Assembly Biosciences (United States)), George Karlin‐Neumann(Assembly Biosciences (United States)), Xiuhua Lu(Baylor College of Medicine), Xin Miao(Assembly Biosciences (United States)), Bridget Moore(Assembly Biosciences (United States)), Martin Moorhead(Assembly Biosciences (United States)), Eugeni Namsaraev(Assembly Biosciences (United States)), Shiran Pasternak(Baylor College of Medicine), Eunice Prakash(Assembly Biosciences (United States)), Karen Tran(Assembly Biosciences (United States)), Zhiyong Wang(Assembly Biosciences (United States)), Hywel B. Jones(Assembly Biosciences (United States)), Ronald W. Davis(Stanford University), T. D. Willis(Assembly Biosciences (United States)), Richard A. Gibbs(Baylor College of Medicine)
Genome Research
February 1, 2005
Cited by 309Open Access
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Abstract

Large-scale genetic studies are highly dependent on efficient and scalable multiplex SNP assays. In this study, we report the development of Molecular Inversion Probe technology with four-color, single array detection, applied to large-scale genotyping of up to 12,000 SNPs per reaction. While generating 38,429 SNP assays using this technology in a population of 30 trios from the Centre d'Etude Polymorphisme Humain family panel as part of the International HapMap project, we established SNP conversion rates of approximately 90% with concordance rates >99.6% and completeness levels >98% for assays multiplexed up to 12,000plex levels. Furthermore, these individual metrics can be "traded off" and, by sacrificing a small fraction of the conversion rate, the accuracy can be increased to very high levels. No loss of performance is seen when scaling from 6,000plex to 12,000plex assays, strongly validating the ability of the technology to suppress cross-reactivity at high multiplex levels. The results of this study demonstrate the suitability of this technology for comprehensive association studies that use targeted SNPs in indirect linkage disequilibrium studies or that directly screen for causative mutations.


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