4.8 Article

Genome sequencing in microfabricated high-density picolitre reactors

Journal

NATURE
Volume 437, Issue 7057, Pages 376-380

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nature03959

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Funding

  1. NHGRI NIH HHS [R01 HG003562-02, P01 HG003022-020002] Funding Source: Medline

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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.

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