Wellcome Trust Sanger Institute, Hinxton, UK.
Biotechniques. 2012 Dec;53(6):365-72. doi: 10.2144/000113962.
We have developed a sequencing method on the Pacific Biosciences RS sequencer (the PacBio) for small DNA molecules that avoids the need for a standard library preparation. To date this approach has been applied toward sequencing single-stranded and double-stranded viral genomes, bacterial plasmids, plasmid vector models for DNA-modification analysis, and linear DNA fragments covering an entire bacterial genome. Using direct sequencing it is possible to generate sequence data from as little as 1 ng of DNA, offering a significant advantage over current protocols which typically require 400-500 ng of sheared DNA for the library preparation.
我们开发了一种在 Pacific Biosciences RS 测序仪(PacBio)上用于小 DNA 分子的测序方法,该方法无需标准文库制备。迄今为止,该方法已应用于测序单链和双链病毒基因组、细菌质粒、用于 DNA 修饰分析的质粒载体模型以及涵盖整个细菌基因组的线性 DNA 片段。使用直接测序,可以从少至 1ng 的 DNA 生成序列数据,与当前通常需要 400-500ng 剪切 DNA 进行文库制备的方案相比,具有显著优势。