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使用红外染料标记引物和自动DNA测序仪进行高通量扩增片段长度多态性分析。

High-throughput AFLP analysis using infrared dye-labeled primers and an automated DNA sequencer.

作者信息

Myburg A A, Remington D L, O'Malley D M, Sederoff R R, Whetten R W

机构信息

Forest Biotechnology Group, Box 7247, Centennial Campus, North Carolina State University, Raleigh, NC 27695, USA.

出版信息

Biotechniques. 2001 Feb;30(2):348-52, 354, 356-7. doi: 10.2144/01302tt04.

Abstract

Amplified fragment length polymorphism (AFLP) analysis is currently the most powerful and efficient technique for the generation of large numbers of anonymous DNA markers in plant and animal genomes. We have developed a protocol for high-throughput AFLP analysis that allows up to 70,000 polymorphic marker genotype determinations per week on a single automated DNA sequencer. This throughput is based on multiplexed PCR amplification of AFLP fragments using two different infrared dyelabeled primer combinations. The multiplexed AFLPs are resolved on a two-dye, model 4200 LI-COR automated DNA sequencer, and the digital images are scored using semi-automated scoring software specifically designed for complex AFLP banding patterns (AFLP-Quantar). Throughput is enhanced by using high-quality genomic DNA templates obtained by a 96-well DNA isolation procedure.

摘要

扩增片段长度多态性(AFLP)分析是目前在植物和动物基因组中生成大量匿名DNA标记最强大、最有效的技术。我们已经开发出一种高通量AFLP分析方案,该方案在单个自动化DNA测序仪上每周可进行多达70000次多态性标记基因型测定。这种通量基于使用两种不同的红外染料标记引物组合对AFLP片段进行多重PCR扩增。多重AFLP在双染料的4200型LI-COR自动化DNA测序仪上进行分离,数字图像使用专门为复杂AFLP条带模式设计的半自动评分软件(AFLP-Quantar)进行评分。通过使用通过96孔DNA分离程序获得的高质量基因组DNA模板提高了通量。

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