Single-Molecule DNA Sequencing of a Viral Genome
Top Cited Papers
- 4 April 2008
- journal article
- other
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 320 (5872) , 106-109
- https://doi.org/10.1126/science.1150427
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.Keywords
This publication has 14 references indexed in Scilit:
- Whole-genome sequencing and variant discovery in C. elegansNature Methods, 2008
- Four-color DNA sequencing by synthesis using cleavable fluorescent nucleotide reversible terminatorsProceedings of the National Academy of Sciences, 2006
- The Consensus Coding Sequences of Human Breast and Colorectal CancersScience, 2006
- Single-Molecule, Motion-Based DNA Sequencing Using RNA PolymeraseScience, 2006
- Accurate Multiplex Polony Sequencing of an Evolved Bacterial GenomeScience, 2005
- Genome sequencing in microfabricated high-density picolitre reactorsNature, 2005
- Advanced sequencing technologies: methods and goalsNature Reviews Genetics, 2004
- The Sequence of the Human GenomeScience, 2001
- Initial sequencing and analysis of the human genomeNature, 2001
- The fidelity of Taq polymerase catalyzing PCR is improved by an N-terminal deletionGene, 1992