首页> 外文期刊>Gene therapy and regulation: An international interdisciplinary journal >HIGH-THROUGHPUT, MASSIVELY PARALLEL DNA SEQUENCING TECHNOLOGY FOR THE ERA OF PERSONALIZED MEDICINE
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HIGH-THROUGHPUT, MASSIVELY PARALLEL DNA SEQUENCING TECHNOLOGY FOR THE ERA OF PERSONALIZED MEDICINE

机译:个性化医学时代的高通量,大规模并行DNA测序技术

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摘要

A challenge to the realization of the vision of personalized medicine is our lack of under standing of the amount of genetic variation contained in the human species, which has been prohibitively expensive to acquire to date. In this review, we discuss a new sys tem based on massively parallel picotiter plate based sequencing. This approach, now commercially available, delivers in excess of 200,000 individual clonal reads in ti single five hour run and hence provides orders of magnitude improvement in speed and cost-over conventional Sanger-based sequencing. The system is scalable well beyond its cur rent performance and its emergence makes plausible the routine sequencing of individual human genomes in the near future. In this review, our .system is presented in light of recent NHGRI sequencing technology grants, and a number of new applications enabled by ready access to hundreds of thousands of individual clonal reads are discussed with a particular focus on their potential impact on human health.
机译:实现个性化医学愿景的一个挑战是,我们缺乏对人类物种中所包含的遗传变异数量的了解,迄今为止,获得这种遗传变异的成本过高。在这篇综述中,我们讨论了一种基于大规模平行微微孔板测序的新系统。该方法现已商业化,每5小时运行一次即可提供超过200,000个单独的克隆读数,因此与基于传统Sanger的测序相比,其速度和成本提高了多个数量级。该系统的可扩展性远远超出其当前的性能,其出现使得在不久的将来对单个人类基因组进行常规测序成为可能。在这篇综述中,我们的.system是根据最近的NHGRI测序技术拨款而提出的,并且讨论了通过随时访问成千上万个单独的克隆读数而启用的许多新应用程序,其中特别关注了它们对人体健康的潜在影响。

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