Margulies Marcel, Egholm Michael, Altman William E, Attiya Said, Bader Joel S, Bemben Lisa A, Berka Jan, Braverman Michael S, Chen Yi-Ju, Chen Zhoutao, Dewell Scott B, Du Lei, Fierro Joseph M, Gomes Xavier V, Godwin Brian C, He Wen, Helgesen Scott, Ho Chun Heen, Irzyk Gerard P, Jando Szilveszter C, Alenquer Maria L I, Jarvie Thomas P, Jirage Kshama B, Kim Jong-Bum, Knight James R, Lanza Janna R, Leamon John H, Lefkowitz Steven M, Lei Ming, Li Jing, Lohman Kenton L, Lu Hong, Makhijani Vinod B, McDade Keith E, McKenna Michael P, Myers Eugene W, Nickerson Elizabeth, Nobile John R, Plant Ramona, Puc Bernard P, Ronan Michael T, Roth George T, Sarkis Gary J, Simons Jan Fredrik, Simpson John W, Srinivasan Maithreyan, Tartaro Karrie R, Tomasz Alexander, Vogt Kari A, Volkmer Greg A, Wang Shally H, Wang Yong, Weiner Michael P, Yu Pengguang, Begley Richard F, Rothberg Jonathan M
454 Life Sciences Corp., 20 Commercial Street, Branford, Connecticut 06405, USA.
Nature. 2005 Sep 15;437(7057):376-80. doi: 10.1038/nature03959. Epub 2005 Jul 31.
The proliferation of large-scale DNA-sequencing projects in recent years has driven a search for alternative methods to reduce time and cost. Here we describe a scalable, highly parallel sequencing system with raw throughput significantly greater than that of state-of-the-art capillary electrophoresis instruments. The apparatus uses a novel fibre-optic slide of individual wells and is able to sequence 25 million bases, at 99% or better accuracy, in one four-hour run. To achieve an approximately 100-fold increase in throughput over current Sanger sequencing technology, we have developed an emulsion method for DNA amplification and an instrument for sequencing by synthesis using a pyrosequencing protocol optimized for solid support and picolitre-scale volumes. Here we show the utility, throughput, accuracy and robustness of this system by shotgun sequencing and de novo assembly of the Mycoplasma genitalium genome with 96% coverage at 99.96% accuracy in one run of the machine.
近年来,大规模DNA测序项目的激增促使人们寻找可替代方法以减少时间和成本。在此,我们描述了一种可扩展的、高度并行的测序系统,其原始通量显著高于目前最先进的毛细管电泳仪器。该仪器使用一种新型的带有单个孔的光纤载玻片,能够在一次四小时的运行中以99%或更高的准确率对2500万个碱基进行测序。为了使通量比当前的桑格测序技术提高约100倍,我们开发了一种用于DNA扩增的乳液法以及一种采用针对固相支持物和皮升规模体积优化的焦磷酸测序方案的合成测序仪器。在此,我们通过对生殖支原体基因组进行鸟枪法测序和从头组装,展示了该系统的实用性、通量、准确性和稳健性,在仪器的一次运行中,覆盖度达到96%,准确率为99.96%。