Genome sequencing in microfabricated high-density picolitre reactors

被引:5266
作者
Margulies, M
Egholm, M
Altman, WE
Attiya, S
Bader, JS
Bemben, LA
Berka, J
Braverman, MS
Chen, YJ
Chen, ZT
Dewell, SB
Du, L
Fierro, JM
Gomes, XV
Godwin, BC
He, W
Helgesen, S
Ho, CH
Irzyk, GP
Jando, SC
Alenquer, MLI
Jarvie, TP
Jirage, KB
Kim, JB
Knight, JR
Lanza, JR
Leamon, JH
Lefkowitz, SM
Lei, M
Li, J
Lohman, KL
Lu, H
Makhijani, VB
McDade, KE
McKenna, MP
Myers, EW
Nickerson, E
Nobile, JR
Plant, R
Puc, BP
Ronan, MT
Roth, GT
Sarkis, GJ
Simons, JF
Simpson, JW
Srinivasan, M
Tartaro, KR
Tomasz, A
Vogt, KA
Volkmer, GA
机构
[1] Life Sci Corp 454, Branford, CT 06405 USA
[2] Univ Calif Berkeley, Berkeley, CA 94720 USA
[3] Rockefeller Univ, Microbiol Lab, New York, NY 10021 USA
[4] Rothberg Inst Childhood Dis, Guilford, CT 06437 USA
关键词
D O I
10.1038/nature03959
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页码:376 / 380
页数:5
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