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完整噬菌体基因组的测序、组装与完成

Sequencing, Assembling, and Finishing Complete Bacteriophage Genomes.

作者信息

Russell Daniel A

机构信息

Department of Biological Sciences, University of Pittsburgh, 344 Crawford Hall, 4249 Fifth Ave, Pittsburgh, PA, 15260, USA.

出版信息

Methods Mol Biol. 2018;1681:109-125. doi: 10.1007/978-1-4939-7343-9_9.

Abstract

Next-generation DNA sequencing (NGS) technologies have made generating genomic sequence for organisms of interest affordable and commonplace. However, NGS platforms and analysis software are generally tuned to be used on large and complex genomes or metagenomic samples. Determining the complete genome sequence of a single bacteriophage requires a somewhat different perspective, workflow, and sensitivity to the nature of phages. Because phage genomes consist of mostly coding regions (see Pope/Jacobs-Sera chapter), a very high standard should be adopted when completing these genomes so that the subsequent steps of annotation and analysis are not sabotaged by sequencing errors. While read quality and assembly algorithms have continued to improve, achieving this standard still requires a significant amount of human oversight and expertise. This chapter describes our workflow for sequencing, assembling, and finishing phage genomes to a high standard by the NGS platforms Illumina, Ion Torrent, and 454.

摘要

新一代DNA测序(NGS)技术已使为感兴趣的生物体生成基因组序列变得经济实惠且司空见惯。然而,NGS平台和分析软件通常是针对大型复杂基因组或宏基因组样本进行优化的。确定单个噬菌体的完整基因组序列需要稍有不同的视角、工作流程以及对噬菌体性质的敏感性。由于噬菌体基因组主要由编码区组成(见波普/雅各布斯 - 塞拉章节),在完成这些基因组时应采用非常高的标准,以便后续的注释和分析步骤不会因测序错误而受到影响。虽然读取质量和组装算法不断改进,但要达到这一标准仍需要大量人工监督和专业知识。本章介绍了我们通过Illumina、Ion Torrent和454等NGS平台对噬菌体基因组进行高标准测序、组装和完成的工作流程。

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