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Cultivating DNA Sequencing Technology After the Human Genome Project.
Annual Review of Genomics and Human Genetics ( IF 8.7 ) Pub Date : 2020-09-01 , DOI: 10.1146/annurev-genom-111919-082433
Jeffery A Schloss 1 , Richard A Gibbs 2 , Vinod B Makhijani 3 , Andre Marziali 4, 5
Affiliation  

When the Human Genome Project was completed in 2003, automated Sanger DNA sequencing with fluorescent dye labels was the dominant technology. Several nascent alternative methods based on older ideas that had not been fully developed were the focus of technical researchers and companies. Funding agencies recognized the dynamic nature of technology development and that, beyond the Human Genome Project, there were growing opportunities to deploy DNA sequencing in biological research. Consequently, the National Human Genome Research Institute of the National Institutes of Health created a program—widely known as the Advanced Sequencing Technology Program—that stimulated all stages of development of new DNA sequencing methods, from innovation to advanced manufacturing and production testing, with the goal of reducing the cost of sequencing a human genome first to $100,000 and then to $1,000. The events of this period provide a powerful example of how judicious funding of academic and commercial partners can rapidly advance core technology developments that lead to profound advances across the scientific landscape.

中文翻译:


人类基因组计划之后的DNA测序技术的培养。

当人类基因组计划于2003年完成时,具有荧光染料标记的Sanger DNA自动测序是主要技术。技术研究人员和公司关注的是一些基于较旧思想的新生方法,这些方法尚未得到充分发展。资助机构认识到技术发展的动态性质,除人类基因组计划外,在生物研究中部署DNA测序的机会越来越多。因此,美国国立卫生研究院的国家人类基因组研究所创建了一个程序,该程序被广泛称为“高级测序技术程序”,该程序刺激了新的DNA测序方法开发的各个阶段,从创新到先进的制造和生产测试,目的是将人类基因组测序的成本首先降低到100,000美元,然后降低到1,000美元。这一时期的事件提供了一个有力的例子,说明学术和商业合作伙伴的明智资助如何能够迅速推动核心技术的发展,从而导致整个科学领域的深刻进步。

更新日期:2020-09-03
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