基因组
底漆(化妆品)
DNA测序
DNA
生物
计算生物学
基因组学
遗传学
序列(生物学)
多重位移放大
顺序装配
聚合酶链反应
人类基因组
DNA纳米球测序
基因组文库
基因
化学
基序列
DNA提取
有机化学
转录组
基因表达
作者
T.D. Harris,Phillip R. Buzby,Hazen P. Babcock,E. George Beer,Jayson Bowers,Ido Braslavsky,Marie Causey,Jennifer Colonell,James J. Dimeo,J. William Efcavitch,Eldar Giladi,Jaime Gill,John Healy,Mirna Jarosz,Dan Lapen,Keith Moulton,Stephen R. Quake,Kathleen E. Steinmann,Edward C. Thayer,Anastasia Tyurina,R. Matthew Ward,Howard Weiss,Zheng Xie
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2008-04-03
卷期号:320 (5872): 106-109
被引量:668
标识
DOI:10.1126/science.1150427
摘要
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 >150x 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.
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