A genome-wide scalable SNP genotyping assay using microarray technology

被引:0
|
作者
Kevin L Gunderson
Frank J Steemers
Grace Lee
Leo G Mendoza
Mark S Chee
机构
[1] Illumina,
[2] Inc.,undefined
[3] Ambion,undefined
[4] Inc.,undefined
[5] 2130 Woodward,undefined
[6] Prognosys Biosciences,undefined
[7] Inc.,undefined
来源
Nature Genetics | 2005年 / 37卷
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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:5
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