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复杂性状的基因剖析

Genetic dissection of complex traits.

作者信息

Lander E S, Schork N J

机构信息

Whitehead Institute for Biomedical Research, Cambridge, MA 02142.

出版信息

Science. 1994 Sep 30;265(5181):2037-48. doi: 10.1126/science.8091226.

Abstract

Medical genetics was revolutionized during the 1980s by the application of genetic mapping to locate the genes responsible for simple Mendelian diseases. Most diseases and traits, however, do not follow simple inheritance patterns. Genetics have thus begun taking up the even greater challenge of the genetic dissection of complex traits. Four major approaches have been developed: linkage analysis, allele-sharing methods, association studies, and polygenic analysis of experimental crosses. This article synthesizes the current state of the genetic dissection of complex traits--describing the methods, limitations, and recent applications to biological problems.

摘要

20世纪80年代,基因图谱的应用彻底改变了医学遗传学,通过基因图谱来定位导致单基因孟德尔疾病的基因。然而,大多数疾病和性状并不遵循简单的遗传模式。因此,遗传学开始着手应对对复杂性状进行基因剖析这一更大的挑战。已经开发出四种主要方法:连锁分析、等位基因共享方法、关联研究以及实验杂交的多基因分析。本文综合了复杂性状基因剖析的当前状况——描述了方法、局限性以及最近在生物学问题中的应用。

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