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QnAs with Eric S. Lander

机译:与Eric S.Lander的QnA

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摘要

This year marks the 10th anniver sary of the sequencing of the hu man genome. More than two decades after the launch of the Human Genome Project, researchers have made remarkable inroads into unraveling human biology, evolution, and disease. As the tools of genome sequencing and analysis grow more sophisticated, insights into the human genome will slowly shift the terrain in the treatment of disease. To be sure, the shift has already begun. Eric Lander, founding director of the Broad Institute of Harvard and Massachusetts Institute of Technology and a member of the National Academy of Sciences, offers PNAS readers his perspectives on the role of genome sequencing in the transfor mation of medicine.
机译:今年是人类基因组测序十周年。在人类基因组计划启动后的二十多年中,研究人员已经在探索人类生物学,进化和疾病方面取得了令人瞩目的进展。随着基因组测序和分析工具变得越来越复杂,对人类基因组的洞察力将在治疗疾病方面缓慢地改变领域。可以肯定的是,这种转变已经开始。哈佛大学博德学院和麻省理工学院的创始主任,美国国家科学院院士埃里克·兰德(Eric Lander)向PNAS读者介绍了他对基因组测序在医学转化中的作用的看法。

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