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使用SISPA对单个分离噬菌斑中的噬菌体进行全基因组测序的扩增

Amplification for Whole Genome Sequencing of Bacteriophages from Single Isolated Plaques Using SISPA.

作者信息

Fouts Derick E

机构信息

J. Craig Venter Institute, 9714 Medical Center Dr, Rockville, MD, 20850, USA.

出版信息

Methods Mol Biol. 2018;1681:165-178. doi: 10.1007/978-1-4939-7343-9_12.

Abstract

Genomics has greatly transformed our understanding of phage biology; however, traditional methods of DNA isolation for whole genome sequencing have required phages to be grown to high titers in large-scale preparations, potentially selecting for only those phages that can grow efficiently under laboratory conditions. This may also select for mutations or deletions that enable more efficient growth in culture. The ability to sequence a bacteriophage genome from a single isolated plaque reduces these risks while decreasing the time and complexity of bacteriophage genome sequencing. A method of amplification and library preparation is described, utilizing Sequence Independent Single Primer Amplification (SISPA), that can be used for whole genome shotgun sequencing of bacteriophages from a single isolated plaque.

摘要

基因组学极大地改变了我们对噬菌体生物学的理解;然而,用于全基因组测序的传统DNA分离方法需要在大规模培养中使噬菌体生长至高滴度,这可能只会选择那些能够在实验室条件下高效生长的噬菌体。这也可能会选择那些能够在培养中更高效生长的突变或缺失。从单个分离的噬菌斑对噬菌体基因组进行测序的能力降低了这些风险,同时减少了噬菌体基因组测序的时间和复杂性。本文描述了一种利用序列无关单引物扩增(SISPA)的扩增和文库制备方法,该方法可用于对单个分离噬菌斑中的噬菌体进行全基因组鸟枪法测序。

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