Barquist Lars, Mayho Matthew, Cummins Carla, Cain Amy K, Boinett Christine J, Page Andrew J, Langridge Gemma C, Quail Michael A, Keane Jacqueline A, Parkhill Julian
Wellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK and Institute for Molecular Infection Biology, University of Würzburg, Würzburg D-97080, Germany.
Wellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK and.
Bioinformatics. 2016 Apr 1;32(7):1109-11. doi: 10.1093/bioinformatics/btw022. Epub 2016 Jan 21.
Transposon insertion sequencing is a high-throughput technique for assaying large libraries of otherwise isogenic transposon mutants providing insight into gene essentiality, gene function and genetic interactions. We previously developed the Transposon Directed Insertion Sequencing (TraDIS) protocol for this purpose, which utilizes shearing of genomic DNA followed by specific PCR amplification of transposon-containing fragments and Illumina sequencing. Here we describe an optimized high-yield library preparation and sequencing protocol for TraDIS experiments and a novel software pipeline for analysis of the resulting data. The Bio-Tradis analysis pipeline is implemented as an extensible Perl library which can either be used as is, or as a basis for the development of more advanced analysis tools. This article can serve as a general reference for the application of the TraDIS methodology.
The optimized sequencing protocol is included as supplementary information. The Bio-Tradis analysis pipeline is available under a GPL license at https://github.com/sanger-pathogens/Bio-Tradis
Supplementary data are available at Bioinformatics online.
转座子插入测序是一种高通量技术,用于分析大量的同基因转座子突变体文库,从而深入了解基因的必需性、基因功能和遗传相互作用。我们之前为此目的开发了转座子定向插入测序(TraDIS)方案,该方案利用基因组DNA的剪切,随后对含转座子的片段进行特异性PCR扩增和Illumina测序。在此,我们描述了一种用于TraDIS实验的优化的高产文库制备和测序方案,以及一种用于分析所得数据的新型软件流程。Bio-Tradis分析流程作为一个可扩展的Perl库实现,既可以直接使用,也可以作为开发更高级分析工具的基础。本文可作为TraDIS方法应用的一般参考。
优化后的测序方案作为补充信息包含在内。Bio-Tradis分析流程可在https://github.com/sanger-pathogens/Bio-Tradis上根据GPL许可获得。
补充数据可在《生物信息学》在线获取。