High-throughput SNP genotyping with the Masscode system

被引:0
|
作者
Kokoris, M [1 ]
Dix, K [1 ]
Moynihan, K [1 ]
Mathis, J [1 ]
Erwin, B [1 ]
Grass, P [1 ]
Hines, B [1 ]
Duesterhoeft, A [1 ]
机构
[1] QIAGEN Genom Inc, Bothell, WA 98021 USA
来源
MOLECULAR DIAGNOSIS | 2000年 / 5卷 / 04期
关键词
single nucleotide polymorphism; mass spectrometry; cleavable mass spectrometry tags; multiplexed detection;
D O I
暂无
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
QIAGEN Genomics, Inc, has developed the Masscode tagging system for DNA labeling and detection. In this application, the Masscode system is described as applied to high-throughput single-nucleotide polymorphism (SNP) genotyping. The labeling system is based on a small-moleculal-weight tag that is covalently attached through a photocleavable linker to a DNA oligonucleotide. The tagged oligonucleotide is used as a primer in an allele-specific PCR SNP discrimination assay. The allele-spscific amplicons are differentiated through their Masscode tag assignments. After a photolysis step to cleave the tags from the amplicon, the samples are introduced into a single quadrupole mass spectrometry detection system for analysis. Genotyping determinations are based on the relative proportions of the paired allele tags. The system has a lower limit of detection in the femtomolar range (10(-15) M). At present, 30 different Masscode tags may be used simultaneously in a multiplex fashion to routinely provide more than 40,000 SNP genotyping measurements daily. Further developments will allow for the simultaneous detection of several hundred tags.
引用
收藏
页码:329 / 340
页数:12
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