Department of Bioengineering, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0412, USA.
Lab Chip. 2010 May 7;10(9):1153-9. doi: 10.1039/b921417h. Epub 2010 Feb 9.
We report the proof of concept of a novel DNA sequencing technology called sequencing by denaturation (SBD). SBD is based on the Sanger sequencing reaction performed on amplified target templates immobilized on a solid surface followed by the denaturation of these Sanger fragments. As these fluorescently labeled fragments denature sequentially, the fluorescence intensities in the four channels corresponding to the four base types are monitored in a flow cell. A sequencing instrument with a microfluidic flowcell has been custom-designed to integrate automated fluidics, temperature control, and fluorescence imaging. The denaturation profiles of several synthetic oligonucleotides were measured with this system and our data demonstrated the ability to sequence short DNA by SBD. SBD is a simple and fast method with the potential to improve the speed and cost of large-scale genome re-sequencing.
我们报告了一种名为变性测序(SBD)的新型 DNA 测序技术的概念验证。SBD 基于在固定在固体表面上的扩增靶标模板上进行的桑格测序反应,然后使这些桑格片段变性。随着这些荧光标记片段依次变性,在四个通道中监测对应于四种碱基类型的荧光强度。已经定制了具有微流控流动池的测序仪器,以集成自动化流体、温度控制和荧光成像。使用该系统测量了几种合成寡核苷酸的变性曲线,并且我们的数据表明 SBD 能够对短 DNA 进行测序。SBD 是一种简单快速的方法,具有提高大规模基因组重测序速度和降低成本的潜力。