Shendure Jay, Porreca Gregory J, Reppas Nikos B, Lin Xiaoxia, McCutcheon John P, Rosenbaum Abraham M, Wang Michael D, Zhang Kun, Mitra Robi D, Church George M
Department of Genetics, Harvard Medical School, Boston, MA 02115, USA.
Science. 2005 Sep 9;309(5741):1728-32. doi: 10.1126/science.1117389. Epub 2005 Aug 4.
We describe a DNA sequencing technology in which a commonly available, inexpensive epifluorescence microscope is converted to rapid nonelectrophoretic DNA sequencing automation. We apply this technology to resequence an evolved strain of Escherichia coli at less than one error per million consensus bases. A cell-free, mate-paired library provided single DNA molecules that were amplified in parallel to 1-micrometer beads by emulsion polymerase chain reaction. Millions of beads were immobilized in a polyacrylamide gel and subjected to automated cycles of sequencing by ligation and four-color imaging. Cost per base was roughly one-ninth as much as that of conventional sequencing. Our protocols were implemented with off-the-shelf instrumentation and reagents.
我们描述了一种DNA测序技术,该技术将常用的、价格低廉的落射荧光显微镜转变为快速非电泳DNA测序自动化设备。我们应用此技术对一株进化的大肠杆菌菌株进行重测序,每百万个一致碱基的错误率低于1个。一个无细胞的配对文库提供了单个DNA分子,这些分子通过乳液聚合酶链反应与1微米的珠子平行扩增。数百万个珠子固定在聚丙烯酰胺凝胶中,并通过连接测序和四色成像进行自动循环测序。每个碱基的成本约为传统测序的九分之一。我们的实验方案采用了现成的仪器和试剂。