Highly multiplexed molecular inversion probe genotyping: Over 10,000 targeted SNPs genotyped in a single tube assay
Open Access
- 1 February 2005
- journal article
- Published by Cold Spring Harbor Laboratory in Genome Research
- Vol. 15 (2) , 269-275
- https://doi.org/10.1101/gr.3185605
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 ∼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.Keywords
This publication has 16 references indexed in Scilit:
- What SNP genotyping errors are most costly for genetic association studies?Genetic Epidemiology, 2004
- The International HapMap ProjectNature, 2003
- Multiplexed genotyping with sequence-tagged molecular inversion probesNature Biotechnology, 2003
- The impact of genotyping error on haplotype reconstruction and frequency estimationEuropean Journal of Human Genetics, 2002
- BeadArray ™ Technology: Enabling an Accurate, Cost-Effective Approach to High-Throughput GenotypingBioTechniques, 2002
- The Autism Genetic Resource Exchange: A Resource for the Study of Autism and Related Neuropsychiatric ConditionsAmerican Journal of Human Genetics, 2001
- Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's diseaseNature, 2001
- Epidemiology and Factor Analysis of Obesity, Type II Diabetes, Hypertension, and Dyslipidemia (Syndrome X) on the Island of Kosrae, Federated States of MicronesiaHuman Heredity, 2000
- Searching for genetic determinants in the new millenniumNature, 2000
- Prospects for whole-genome linkage disequilibrium mapping of common disease genesNature Genetics, 1999