Genome sequencing in microfabricated high-density picolitre reactors

2005 Nature 7,613 citations

Abstract

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.

Keywords

Sanger sequencingDNA sequencingShotgun sequencingMassive parallel sequencingPyrosequencingComputational biologySequence assemblyScalabilityComputer scienceThroughputMetagenomicsGenomeBiologyDNAGeneticsGeneDatabaseTranscriptome

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Publication Info

Year
2005
Type
article
Volume
437
Issue
7057
Pages
376-380
Citations
7613
Access
Closed

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Cite This

Marcel Margulies, Michael D. Miller, William E. Altman et al. (2005). Genome sequencing in microfabricated high-density picolitre reactors. Nature , 437 (7057) , 376-380. https://doi.org/10.1038/nature03959

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DOI
10.1038/nature03959