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多重PCR用户的福音:MPprimer and MFEprimer

已有 6560 次阅读 2010-4-17 23:59 |个人分类:科学观察|系统分类:论文交流|关键词:学者| PCR, 多重PCR, MPprimer, MFEprimer

最近我们实验室在BMC Bioinformatics上发表了多重PCR引物设计程序MPprimer,对于提高PCR实验的效率具有一定帮助,有兴趣的朋友可以看看:

http://www.biomedcentral.com/1471-2105/11/143/abstract

Software

MPprimer: a program for reliable multiplex PCR primer design

Zhiyong Shen email, Wubin Qu email, Wen Wang email, Yiming Lu email, Yonghong Wu email, Zhifeng Li email, Xingyi Hang email, Xiaolei Wang email, Dongsheng Zhao email and Chenggang Zhang email

BMC Bioinformatics 2010, 11:143doi:10.1186/1471-2105-11-143

 
Published: 18 March 2010

Abstract (provisional)

Background

Multiplex PCR, defined as the simultaneous amplification of multiple regions of a DNA template or multiple DNA templates using more than one primer set (comprising a forward primer and a reverse primer) in one tube, has been widely used in diagnostic applications of clinical and environmental microbiology studies. However, primer design for multiplex PCR is still a challenging problem and several factors need to be considered. These problems include mis-priming due to nonspecific binding to non-target DNA templates, primer dimerization, and the inability to separate and purify DNA amplicons with similar electrophoretic mobility.

Results

A program named MPprimer was developed to help users for reliable multiplex PCR primer design. It employs the widely used primer design program Primer3 and the primer specificity evaluation program MFEprimer to design and evaluate the candidate primers based on genomic or transcript DNA database, followed by careful examination to avoid primer dimerization. The graph-expanding algorithm derived from the greedy algorithm was used to determine the optimal primer set combinations (PSCs) for multiplex PCR assay. In addition, MPprimer provides a virtual electrophotogram to help users choose the best PSC. The experimental validation from 2x to 5x plex PCR demonstrates the reliability of MPprimer. As another example, MPprimer is able to design the multiplex PCR primers for DMD (dystrophin gene which caused Duchenne Muscular Dystrophy), which has 79 exons, for 20x, 20x, 20x, 14x, and 5x plex PCR reactions in five tubes to detect underlying exon deletions.

Conclusions

MPprimer is a valuable tool for designing specific, non-dimerizing primer set combinations with constrained amplicons size for multiplex PCR assays.



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