Single-Molecule DNA Sequencing of a Viral Genome

Author:

Harris Timothy D.123,Buzby Phillip R.123,Babcock Hazen123,Beer Eric123,Bowers Jayson123,Braslavsky Ido123,Causey Marie123,Colonell Jennifer123,DiMeo James123,Efcavitch J. William123,Giladi Eldar123,Gill Jaime123,Healy John123,Jarosz Mirna123,Lapen Dan123,Moulton Keith123,Quake Stephen R.123,Steinmann Kathleen123,Thayer Edward123,Tyurina Anastasia123,Ward Rebecca123,Weiss Howard123,Xie Zheng123

Affiliation:

1. Helicos BioSciences Corporation, One Kendall Square, Cambridge, MA 02139, USA.

2. Department of Physics and Astronomy, Ohio University, Athens, OH 45701, USA.

3. Department of Bioengineering, Stanford University, and Howard Hughes Medical Institute, Stanford, CA 94305, USA.

Abstract

The full promise of human genomics will be realized only when the genomes of thousands of individuals can be sequenced for comparative analysis. A reference sequence enables the use of short read length. We report an amplification-free method for determining the nucleotide sequence of more than 280,000 individual DNA molecules simultaneously. A DNA polymerase adds labeled nucleotides to surface-immobilized primer-template duplexes in stepwise fashion, and the asynchronous growth of individual DNA molecules was monitored by fluorescence imaging. Read lengths of >25 bases and equivalent phred software program quality scores approaching 30 were achieved. We used this method to sequence the M13 virus to an average depth of >150× and with 100% coverage; thus, we resequenced the M13 genome with high-sensitivity mutation detection. This demonstrates a strategy for high-throughput low-cost resequencing.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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