单分子实时测序
碱基对
DNA聚合酶
DNA
DNA纳米球测序
聚合酶
结扎测序
DNA钳
杂交测序
DNA测序
生物
计算生物学
分子生物学
化学
遗传学
聚合酶链反应
基因
基序列
逆转录酶
基因组文库
DNA测序器
作者
Jonas Korlach,Keith P. Bjornson,Bidhan Chaudhuri,Ronald L. Cicero,Benjamin A Flusberg,Jeremy Gray,David W. Holden,R. C. Saxena,Jeffrey Wegener,Stephen W. Turner
标识
DOI:10.1016/s0076-6879(10)72001-2
摘要
Pacific Biosciences has developed a method for real-time sequencing of single DNA molecules (Eid et al., 2009), with intrinsic sequencing rates of several bases per second and read lengths into the kilobase range. Conceptually, this sequencing approach is based on eavesdropping on the activity of DNA polymerase carrying out template-directed DNA polymerization. Performed in a highly parallel operational mode, sequential base additions catalyzed by each polymerase are detected with terminal phosphate-linked, fluorescence-labeled nucleotides. This chapter will first outline the principle of this single-molecule, real-time (SMRT™) DNA sequencing method, followed by descriptions of its underlying components and typical sequencing run conditions. Two examples are provided which illustrate that, in addition to the DNA sequence, the dynamics of DNA polymerization from each enzyme molecules is directly accessible: the determination of base-specific kinetic parameters from single-molecule sequencing reads, and the characterization of DNA synthesis rate heterogeneities.
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