A genome-wide scalable SNP genotyping assay using microarray technology

被引:451
|
作者
Gunderson, KL
Steemers, FJ
Lee, G
Mendoza, LG
Chee, MS
机构
[1] Illumina Inc, San Diego, CA 92121 USA
[2] Ambion Inc, Austin, TX 78744 USA
[3] Prognosys Biosci Inc, San Diego, CA 92121 USA
关键词
D O I
10.1038/ng1547
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Oligonucleotide probe arrays have enabled massively parallel analysis of gene expression levels from a single cDNA sample. Application of microarray technology to analyzing genomic DNA has been stymied by the sequence complexity of the entire human genome. A robust, single base - resolution direct genomic assay would extend the reach of microarray technology. We developed an array-based whole-genome genotyping assay that does not require PCR and enables effectively unlimited multiplexing. The assay achieves a high signal-to-noise ratio by combining specific hybridization of picomolar concentrations of whole genome - amplified DNA to arrayed probes with allele-specific primer extension and signal amplification. As proof of principle, we genotyped several hundred previously characterized SNPs. The conversion rate, call rate and accuracy were comparable to those of high-performance PCR-based genotyping assays.
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页码:549 / 554
页数:6
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