Steinmann Kathleen E, Hart Christopher E, Thompson John F, Milos Patrice M
Helicos BioSciences Corporation, Cambridge, MA, USA.
Methods Mol Biol. 2011;733:3-24. doi: 10.1007/978-1-61779-089-8_1.
With the advent of high-throughput sequencing technologies, multiple bacterial genomes can be sequenced in days. While the ultimate goal of de novo assembly of bacterial genomes is progressing, changes in the genomic sequence of closely related bacterial strains and isolates are now easily monitored by comparison of their sequences to those of a reference genome. Such studies can be applied to the fields of bacterial evolution, epidemiology, and diagnostics. We present a protocol for single-molecule sequencing of bacterial DNA whose end result is the identification of single nucleotide variants, and various size insertions and deletions relative to a reference genome. The protocol is characterized by the simplicity of sample preparation and the lack of amplification-related sequencing bias.
随着高通量测序技术的出现,在数天内就可以对多个细菌基因组进行测序。虽然细菌基因组的从头组装的最终目标仍在推进,但现在通过将密切相关的细菌菌株和分离株的基因组序列与参考基因组进行比较,就可以轻松监测其基因组序列的变化。此类研究可应用于细菌进化、流行病学和诊断领域。我们提出了一种用于细菌DNA单分子测序的方案,其最终结果是识别相对于参考基因组的单核苷酸变异以及各种大小的插入和缺失。该方案的特点是样品制备简单,且不存在与扩增相关的测序偏差。