MPprimer: a program for reliable multiplex PCR primer design

<p>Abstract</p> <p>Background</p> <p>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 u...

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Main Authors: Wang Xiaolei, Hang Xingyi, Li Zhifeng, Wu Yonghong, Lu Yiming, Wang Wen, Qu Wubin, Shen Zhiyong, Zhao Dongsheng, Zhang Chenggang
Format: Article
Language:English
Published: BMC 2010-03-01
Series:BMC Bioinformatics
Online Access:http://www.biomedcentral.com/1471-2105/11/143
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spelling doaj-1b96484e5f4748148db51959cafeae852020-11-25T00:42:24ZengBMCBMC Bioinformatics1471-21052010-03-0111114310.1186/1471-2105-11-143MPprimer: a program for reliable multiplex PCR primer designWang XiaoleiHang XingyiLi ZhifengWu YonghongLu YimingWang WenQu WubinShen ZhiyongZhao DongshengZhang Chenggang<p>Abstract</p> <p>Background</p> <p>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.</p> <p>Results</p> <p>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 2× to 5× 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 20×, 20×, 20×, 14×, and 5× plex PCR reactions in five tubes to detect underlying exon deletions.</p> <p>Conclusions</p> <p>MPprimer is a valuable tool for designing specific, non-dimerizing primer set combinations with constrained amplicons size for multiplex PCR assays.</p> http://www.biomedcentral.com/1471-2105/11/143
collection DOAJ
language English
format Article
sources DOAJ
author Wang Xiaolei
Hang Xingyi
Li Zhifeng
Wu Yonghong
Lu Yiming
Wang Wen
Qu Wubin
Shen Zhiyong
Zhao Dongsheng
Zhang Chenggang
spellingShingle Wang Xiaolei
Hang Xingyi
Li Zhifeng
Wu Yonghong
Lu Yiming
Wang Wen
Qu Wubin
Shen Zhiyong
Zhao Dongsheng
Zhang Chenggang
MPprimer: a program for reliable multiplex PCR primer design
BMC Bioinformatics
author_facet Wang Xiaolei
Hang Xingyi
Li Zhifeng
Wu Yonghong
Lu Yiming
Wang Wen
Qu Wubin
Shen Zhiyong
Zhao Dongsheng
Zhang Chenggang
author_sort Wang Xiaolei
title MPprimer: a program for reliable multiplex PCR primer design
title_short MPprimer: a program for reliable multiplex PCR primer design
title_full MPprimer: a program for reliable multiplex PCR primer design
title_fullStr MPprimer: a program for reliable multiplex PCR primer design
title_full_unstemmed MPprimer: a program for reliable multiplex PCR primer design
title_sort mpprimer: a program for reliable multiplex pcr primer design
publisher BMC
series BMC Bioinformatics
issn 1471-2105
publishDate 2010-03-01
description <p>Abstract</p> <p>Background</p> <p>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.</p> <p>Results</p> <p>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 2× to 5× 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 20×, 20×, 20×, 14×, and 5× plex PCR reactions in five tubes to detect underlying exon deletions.</p> <p>Conclusions</p> <p>MPprimer is a valuable tool for designing specific, non-dimerizing primer set combinations with constrained amplicons size for multiplex PCR assays.</p>
url http://www.biomedcentral.com/1471-2105/11/143
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