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Nature ; 437(7057): 376-80, 2005 Sep 15.
Article in English | MEDLINE | ID: mdl-16056220

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.


Subject(s)
Genome, Bacterial , Genomics/instrumentation , Microchemistry/instrumentation , Mycoplasma genitalium/genetics , Sequence Analysis, DNA/instrumentation , Electrophoresis, Capillary , Emulsions , Fiber Optic Technology , Genomics/economics , Microchemistry/economics , Polymerase Chain Reaction , Reproducibility of Results , Sensitivity and Specificity , Sequence Analysis, DNA/economics , Time Factors
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