亚硫酸氢盐测序
底漆(化妆品)
亚硫酸氢盐
DNA甲基化
CpG站点
背景(考古学)
甲基化
照明菌甲基化试验
生物
计算生物学
硅胶PCR
表观遗传学
遗传学
DNA测序
聚合酶链反应
DNA
分子生物学
基因
多重聚合酶链反应
化学
基因表达
古生物学
有机化学
作者
Long-Cheng Li,Rajvir Dahiya
出处
期刊:Bioinformatics
[Oxford University Press]
日期:2002-11-01
卷期号:18 (11): 1427-1431
被引量:2738
标识
DOI:10.1093/bioinformatics/18.11.1427
摘要
Abstract Motivation: DNA methylation is an epigenetic mechanism of gene regulation. Bisulfite- conversion-based PCR methods, such as bisulfite sequencing PCR (BSP) and methylation specific PCR (MSP), remain the most commonly used techniques for methylation mapping. Existing primer design programs developed for standard PCR cannot handle primer design for bisulfite-conversion-based PCRs due to changes in DNA sequence context caused by bisulfite treatment and many special constraints both on the primers and the region to be amplified for such experiments. Therefore, the present study was designed to develop a program for such applications. Results: MethPrimer, based on Primer3, is a program for designing PCR primers for methylation mapping. It first takes a DNA sequence as its input and searches the sequence for potential CpG islands. Primers are then picked around the predicted CpG islands or around regions specified by users. MethPrimer can design primers for BSP and MSP. Results of primer selection are delivered through a web browser in text and in graphic view. Availability: MethPrimer is freely accessible at the following Web address http://itsa.ucsf.edu/~urolab/methprimer Contact: longli@itsa.ucsf.eduurologylab@aol.com * To whom correspondence should be addressed.
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