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通过192孔MADGE、扩增阻滞突变系统(ARMS)和计算机化凝胶图像分析相结合的单核苷酸多态性(SNP)基因分型。

SNP genotyping by combination of 192-well MADGE, ARMS and computerized gel image analysis.

作者信息

O'Dell S D, Gaunt T R, Day I N

机构信息

Human Genetics Research Division, Southampton University Medical School, Southampton General Hospital, England, UK. s.d.o'

出版信息

Biotechniques. 2000 Sep;29(3):500-4, 505-6. doi: 10.2144/00293st01.

Abstract

A new modification of the microplate array diagonal gel electrophoresis (MADGE) system accommodates the dual amplification refractory mutation system (ARMS) products of 96 samples on one 192-well gel. Simultaneous electrophoresis of a number of horizontal ARMS-MADGE gels achieves high throughput. Gels are imaged digitally, here using the FluorImager 595 fluorescent scanning system. Customized software by Phoretix enables rapid computerized calling of band patterns in ARMS-MADGE arrays, in which the two wells receiving a pair of allele-specific assays for a single template are juxtaposed to form one virtual track, with genotype data exported directly into Microsoft Excel for statistical analysis. An ARMS assay of the A/T base change at the -23/HphI RFLP in the insulin gene promoter, which initiates from 2.5 ng template DNA, was used here to demonstrate this improved general approach for population SNP analyses.

摘要

微板阵列对角线凝胶电泳(MADGE)系统的一种新改进方法可在一块192孔凝胶上容纳96个样本的双重扩增不应突变系统(ARMS)产物。同时电泳多个水平的ARMS-MADGE凝胶可实现高通量。凝胶通过数字成像,此处使用FluorImager 595荧光扫描系统。Phoretix公司的定制软件能够快速对ARMS-MADGE阵列中的条带模式进行计算机化识别,其中接收针对单个模板的一对等位基因特异性检测的两个孔并列形成一条虚拟泳道,基因型数据可直接导出到Microsoft Excel中进行统计分析。在此使用从2.5 ng模板DNA起始的胰岛素基因启动子中-23/HphI限制性片段长度多态性(RFLP)处A/T碱基变化的ARMS检测,来证明这种改进的总体方法用于群体单核苷酸多态性(SNP)分析。

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