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

被引:214
作者
Hardenbol, P
Yu, FL
Belmont, J
MacKenzie, J
Bruckner, C
Brundage, T
Boudreau, A
Chow, S
Eberle, J
Erbilgin, A
Falkowski, M
Fitzgerald, R
Ghose, S
Iartchouk, O
Jain, M
Karlin-Neumann, G
Lu, XH
Miao, X
Moore, B
Moorhead, M
Namsaraev, E
Pasternak, S
Prakash, E
Tran, K
Wang, ZY
Jones, HB
Davis, RW
Willis, TD [1 ]
Gibbs, RA
机构
[1] ParAllele BioSci Inc, San Francisco, CA 94080 USA
[2] Baylor Coll Med, Human Genome Sequencing Ctr, Houston, TX 77030 USA
[3] Stanford Univ, Stanford Genome Technol Ctr, Stanford, CA 94305 USA
关键词
D O I
10.1101/gr.3185605
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 Lip 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 similar to90% 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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收藏
页码:269 / 275
页数:7
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