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使用PrimerXL进行靶向重测序的高通量PCR检测设计

High-throughput PCR assay design for targeted resequencing using primerXL.

作者信息

Lefever Steve, Pattyn Filip, De Wilde Bram, Coppieters Frauke, De Keulenaer Sarah, Hellemans Jan, Vandesompele Jo

机构信息

Center for Medical Genetics, Ghent University, De Pintelaan 185, 9000, Ghent, Belgium.

pxlence, 9200, Dendermonde, Belgium.

出版信息

BMC Bioinformatics. 2017 Sep 6;18(1):400. doi: 10.1186/s12859-017-1809-3.

Abstract

BACKGROUND

Although the sequencing landscape is rapidly evolving and sequencing costs are continuously decreasing, whole genome sequencing is still too expensive for use on a routine basis. Targeted resequencing of only the regions of interest decreases both costs and the complexity of the downstream data-analysis. Various target enrichment strategies are available, but none of them obtain the degree of coverage uniformity, flexibility and specificity of PCR-based enrichment. On the other hand, the biggest limitation of target enrichment by PCR is the need to design large numbers of partially overlapping assays to cover the target.

RESULTS

To overcome the aforementioned hurdles, we have developed primerXL, a state-of-the-art PCR primer design pipeline for targeted resequencing. It uses an optimized design criteria relaxation cascade and a thorough downstream in silico evaluation process to generate high quality singleplex PCR assays, reducing the need for amplicon normalization, and outperforming other target enrichment strategies and similar primer design tools when considering assay quality, coverage uniformity and target coverage. Results of four different sequencing projects with 2348 amplicons in total covering 470 kb are presented. PrimerXL can be accessed at www.primerxl.org .

CONCLUSION

PrimerXL is an state-of-the-art, easy to use primer design webtool capable of generating high-quality targeted resequencing assays. The workflow is fully customizable to suit every researchers' needs, while an innovative relaxation cascade ensures maximal target coverage.

摘要

背景

尽管测序技术正在迅速发展,测序成本也在不断降低,但全基因组测序在常规应用中仍然过于昂贵。仅对感兴趣的区域进行靶向重测序既降低了成本,也降低了下游数据分析的复杂性。目前有多种靶标富集策略,但没有一种能达到基于PCR富集的覆盖均匀度、灵活性和特异性。另一方面,基于PCR的靶标富集的最大限制是需要设计大量部分重叠的检测方法来覆盖靶标。

结果

为了克服上述障碍,我们开发了PrimerXL,这是一种用于靶向重测序的先进PCR引物设计流程。它使用优化的设计标准松弛级联和全面的下游计算机模拟评估过程来生成高质量的单重PCR检测方法,减少了对扩增子标准化的需求,并且在检测质量、覆盖均匀度和靶标覆盖方面优于其他靶标富集策略和类似的引物设计工具。本文展示了四个不同测序项目的结果,总共2348个扩增子,覆盖470 kb。可通过www.primerxl.org访问PrimerXL。

结论

PrimerXL是一种先进的、易于使用的引物设计网络工具,能够生成高质量的靶向重测序检测方法。工作流程完全可定制,以满足每个研究人员的需求,同时创新的松弛级联确保最大的靶标覆盖。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3804/5588703/5b172b57f5cc/12859_2017_1809_Fig1_HTML.jpg

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