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Will long-read sequencing technologies replace short-read sequencing technologies in the next 10 years?

机译:将在未来10年内取代短读测序技术是否会更换缩小读取技术吗?

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The year 1977 is quite remarkable in the history of genomics. It was the first time that thecomplete genome of an organism (phage ΦX174) would be sequenced – the advent of the firstgeneration of sequencing technologies. Of the two sequencing methods published that year,Fred Sanger’s ‘chain-termination’ method would become the mainstay of sequencing technologyfor the next three decades. Because of its better usability compared to the Maxam-Gilbertmethod, it was widely preferred and became commercialised1 by Applied Biosystems Inc.Thanks to the collaborative efforts of scientists across the world,2 Sanger sequencing eventuallyproduced a reference human genome, courtesy of the US$2.7-billion (United States dollar)Human Genome Project completed in 2003.
机译:1977年在基因组学的历史中非常出色。这是第一次将有机体(噬菌体φX174)的基因组第一次进行测序 - 排序技术的第一步的出现。在那一年发布的两种测序方法中,Fred Sanger的“链终止”方法将成为未来三十年来测序技术的主干。由于其与Maxam-Gilbertmethod相比的更好的可用性,它被应用的Biosystems Inc.Chanks致以广泛的商业化,并成为世界各地科学家的协作努力,2 Sanger测序最终提出了一个参考人类基因组,由2.7美元提供礼貌亿(美国美元)人类基因组项目于2003年完成。

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