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PrimerSuite:一种高通量基于网络的多重亚硫酸氢盐 PCR 引物设计程序。

PrimerSuite: A High-Throughput Web-Based Primer Design Program for Multiplex Bisulfite PCR.

机构信息

Centre for Personalized NanoMedicine, The University of Queensland, St Lucia 4072, QLD, Australia.

Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, St Lucia 4072, QLD, Australia.

出版信息

Sci Rep. 2017 Jan 24;7:41328. doi: 10.1038/srep41328.

DOI:10.1038/srep41328
PMID:28117430
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5259761/
Abstract

The analysis of DNA methylation at CpG dinucleotides has become a major research focus due to its regulatory role in numerous biological processes, but the requisite need for assays which amplify bisulfite-converted DNA represents a major bottleneck due to the unique design constraints imposed on bisulfite-PCR primers. Moreover, a review of the literature indicated no available software solutions which accommodated both high-throughput primer design, support for multiplex amplification assays, and primer-dimer prediction. In response, the tri-modular software package PrimerSuite was developed to support bisulfite multiplex PCR applications. This software was constructed to (i) design bisulfite primers against multiple regions simultaneously (PrimerSuite), (ii) screen for primer-primer dimerizing artefacts (PrimerDimer), and (iii) support multiplex PCR assays (PrimerPlex). Moreover, a major focus in the development of this software package was the emphasis on extensive empirical validation, and over 1300 unique primer pairs have been successfully designed and screened, with over 94% of them producing amplicons of the expected size, and an average mapping efficiency of 93% when screened using bisulfite multiplex resequencing. The potential use of the software in other bisulfite-based applications such as methylation-specific PCR is under consideration for future updates. This resource is freely available for use at PrimerSuite website (www.primer-suite.com).

摘要

由于 CpG 二核苷酸中的 DNA 甲基化在许多生物过程中的调节作用,其分析已成为主要的研究焦点,但由于对亚硫酸氢盐-PCR 引物施加了独特的设计限制,因此需要扩增经亚硫酸氢盐转化的 DNA 的测定方法,这是一个主要的瓶颈。此外,文献综述表明,没有可用的软件解决方案可以同时适应高通量引物设计、支持多重扩增测定以及引物二聚体预测。有鉴于此,开发了三模块软件包 PrimerSuite 来支持亚硫酸氢盐多重 PCR 应用。该软件的构建目的是:(i) 同时针对多个区域设计亚硫酸氢盐引物(PrimerSuite);(ii) 筛选引物-引物二聚体假阳性(PrimerDimer);以及 (iii) 支持多重 PCR 测定(PrimerPlex)。此外,该软件包开发的一个重点是强调广泛的实证验证,已经成功设计和筛选了 1300 多个独特的引物对,其中超过 94%的引物对产生了预期大小的扩增子,并且在使用亚硫酸氢盐多重重测序进行筛选时的平均映射效率为 93%。该软件在其他基于亚硫酸氢盐的应用(如甲基化特异性 PCR)中的潜在用途正在考虑在未来的更新中进行。该资源可在 PrimerSuite 网站(www.primer-suite.com)上免费使用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4156/5259761/eb00101122e6/srep41328-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4156/5259761/aaaccef5e156/srep41328-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4156/5259761/f89728324594/srep41328-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4156/5259761/4682d6d512b5/srep41328-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4156/5259761/bb3b9d247847/srep41328-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4156/5259761/eb00101122e6/srep41328-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4156/5259761/aaaccef5e156/srep41328-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4156/5259761/f89728324594/srep41328-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4156/5259761/4682d6d512b5/srep41328-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4156/5259761/bb3b9d247847/srep41328-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4156/5259761/eb00101122e6/srep41328-f5.jpg

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