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1000 Genomes Project Promises Closer Look at Variation in Human Genome

机译:1000个基因组计划有望更深入地研究人类基因组的变异

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A new, large-scale publicscience project is developing a more detailed picture of variations in the human genome that may one day aid scientists' understanding of the genetic basis of disease.Building on the data and technology generated in previous "big science" projects, such as the Human Genome Project and the HapMap (an effort aimed at describing the common patterns of genetic variation in humans), investigators for the 1000 Genomes Project plan to develop an extensive catalog of variation in the human genome by sequencing the genomes of at least 1000 individuals from around the world. The project is being carried out by an international consortium of researchers, including scientists from the National Human Genome Research Institute in Bethesda, Md; the Wellcome Trust Sanger Institutein Hinxton, England, and the Beijing Genomics Institute in Shenzen, China. The first official data from the project will be released in January 2009, said David Altshuler, MD, PhD, co-chair of the consortium and professor of genetics and medicine at Harvard Medical School in Boston, Mass.
机译:一个新的大规模公共科学项目正在开发更详细的人类基因组变化图,有朝一日可以帮助科学家了解疾病的遗传基础。在以前的“大科学”项目中产生的数据和技术的基础上,例如“人类基因组计划”和“ HapMap”(旨在描述人类遗传变异的常见模式),“ 1000个基因组计划”的研究人员计划通过至少对基因组进行测序来开发人类基因组变异的广泛目录来自世界各地的1000个人。该项目由国际研究人员联盟执行,包括来自马里兰州贝塞斯达国家人类基因组研究所的科学家;英国Hinxton的Wellcome Trust Sanger研究所和中国深圳的北京基因组研究所。该项目联合主席,麻省波士顿哈佛医学院遗传与医学教授戴维·奥特舒勒(David Altshuler)表示,该项目的首批官方数据将于2009年1月发布。

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