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Technical Report
Nature Genetics  37, 549 - 554 (2005)
Published online: 17 April 2005; | doi:10.1038/ng1547

A genome-wide scalable SNP genotyping assay using microarray technology

Kevin L Gunderson1, Frank J Steemers1, 4, Grace Lee1, 4, Leo G Mendoza2 & Mark S Chee3

1  Illumina, Inc., 9885 Towne Centre Dr., San Diego, California 92121, USA.

2  Ambion, Inc., 2130 Woodward, Austin, Texas 78744, USA.

3  Prognosys Biosciences, Inc., 4215 Sorrento Valley Blvd., Suite 105, San Diego, California 92121, USA.

4  These authors contributed equally to this work.

Correspondence should be addressed to Kevin L Gunderson kgunderson@illumina.com
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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Nature Genetics
ISSN: 1061-4036
EISSN: 1546-1718
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