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国际人类基因组单体型图计划对人类遗传变异的见解。

Perspectives on human genetic variation from the HapMap Project.

作者信息

McVean Gil, Spencer Chris C A, Chaix Raphaelle

机构信息

Department of Statistics, University of Oxford, Oxford, United Kingdom.

出版信息

PLoS Genet. 2005 Oct;1(4):e54. doi: 10.1371/journal.pgen.0010054.

Abstract

The completion of the International HapMap Project marks the start of a new phase in human genetics. The aim of the project was to provide a resource that facilitates the design of efficient genome-wide association studies, through characterising patterns of genetic variation and linkage disequilibrium in a sample of 270 individuals across four geographical populations. In total, over one million SNPs have been typed across these genomes, providing an unprecedented view of human genetic diversity. In this review we focus on what the HapMap Project has taught us about the structure of human genetic variation and the fundamental molecular and evolutionary processes that shape it.

摘要

国际人类基因组单体型图计划的完成标志着人类遗传学进入了一个新阶段。该计划的目标是通过对来自四个地理群体的270个个体样本中的遗传变异模式和连锁不平衡进行特征分析,提供一种有助于设计高效全基因组关联研究的资源。总共在这些基因组中检测了超过一百万个单核苷酸多态性(SNP),为人类遗传多样性提供了前所未有的视角。在这篇综述中,我们重点关注人类基因组单体型图计划让我们了解到的人类遗传变异结构以及塑造这种结构的基本分子和进化过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acb8/1270010/73b4ae64975b/pgen.0010054.g001.jpg

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