Short tandem repeat typing by capillary array electrophoresis: Comparison of sizing accuracy and precision using different buffer systems

被引:26
作者
Vainer, M [1 ]
Enad, S [1 ]
Dolnik, V [1 ]
Xu, D [1 ]
Bashkin, J [1 ]
Marsh, M [1 ]
Tu, O [1 ]
Harris, DW [1 ]
Barker, DL [1 ]
Mansfield, ES [1 ]
机构
[1] MOL DYNAM INC,SUNNYVALE,CA 94086
关键词
D O I
10.1006/geno.1997.4608
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
Polymorphic microsatellite markers are widely used in gene discovery and mapping, human identification, agricultural genetics, and diagnosis of triplet-repeat expansion disorders. Reliable genotyping of these markers requires polymerase chain reaction (PCR) amplification and very-high-resolution electrophoresis. Capillary array electrophoresis offers extremely fast, high-resolution separation of DNA and more automated sample processing because labor-intensive slab-gel pouring and sample loading are eliminated. We report a simple, reliable procedure for preparing PCR samples for electrokinetic injection into capillaries using a 96-well tray and float dialysis. We developed an improved sizing standard for genotyping and used it to evaluate systematically the sizing accuracy and precision of low-viscosity, replaceable matrix formulations. Our study sizing over 28,000 alleles yielded an average precision of +/- 0.12 bp for fragments up to 350 bp. Low-viscosity formulations permit low-pressure matrix injection (40 psi) and a turnaround time of 70 min for 48-96 samples. (C) 1997 Academic Press.
引用
收藏
页码:1 / 9
页数:9
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