Whole-genome genotyping of haplotype tag single nucleotide polymorphisms

被引:57
作者
Gunderson, KL [1 ]
Kuhn, KM [1 ]
Steemers, FJ [1 ]
Ng, P [1 ]
Murray, SS [1 ]
Shen, R [1 ]
机构
[1] Illumina Inc, San Diego, CA 92121 USA
关键词
ASPE; association; genotyping; haplotype; infinium; linkage disequilibrium; SBE; SNP; tag SNP; whole-genome genotyping;
D O I
10.2217/14622416.7.4.641
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The International HapMap Consortium recently completed gencityping over 3.8 million single nuclecitide polymorphisms (SNPs) in three major populations, and the results of studying patterns of linkage disequilibrium indicate that characterization of 300,000-500,000 tag SNPs is sufficient to provide good genomic coverage for linkage-disequilibrium-based association studies in many populations. These whole-genome association studies will be used to dissect the genetics of complex diseases and pharmacogenomic drug responses. As such, the development of a cost-effective gencityping platform that can assay hundred of thousands of SNPs across thousands of samples is essential. In this review, we describe the development of a whole-genome gencityping (WGG) assay that enables unconstrained SNP selection and effectively unlimited multiplexing from a single sample preparation. The development of WGG in concert with high-density BeadChipS (TM) has enabled the creation of three different high-density SNP gencityping BeadChips: the Sentrix (TM) Human-1 Genotyping BeadChip containing over 109,000 exon-centric SNPs; the HumanHap300 BeadChip containing over 317,000 tag SNPs, and the HumanHap550 Beadchip containing over 550,000 tag SNPs.
引用
收藏
页码:641 / 648
页数:8
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