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Future of genetic epidemiology in complex traits

机译:复杂性状遗传流行病学的未来

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Genetic epidemiology has advanced from its early focus on rare mendelian diseases to the genetic dissection of complex traits. With the advent of the complete genome map of humans and other organisms, more than ever genetic epidemiology has an important role in ascertaining the relative importance of genetic and environment causative factors of complex traits. The main methodology strategies (familial resemblance, segregation analysis, association and linkage analysis and meta-analysis) in the study of complex traits are outlined and its advantages and shortcomings are discussed. The importance of sampling and the use of appropriate phenotypes and genetic markers are stressed and an example on the study of BMI (Body Mass Index), showing the role of a major genetic factor located at chromosome 7 illustrates some of the above strategies. It is suggested that in the future, although recognizing that multiplex families will still be the mainstay of linkage studies, new and efficient types of sampling (unrelated controls, for instance) utilizing pooled DNA samples will be universally employed. The recognition of genetic heterogeneity between studies and its interpretation will be one of the proeminent features in the forthcoming complex traits studies.
机译:遗传流行病学从早期关注罕见的孟塞尔疾病到复杂性状的遗传解剖。随着人类和其他生物的完整基因组图的出现,比以往任何时候都在确定复杂性状的遗传和环境造成因素的相对重要性方面具有重要作用。概述了复杂性状研究中的主要方法策略(家族相比,分析分析,关联和联动分析和荟萃分析),并讨论了其优点和缺点。对抽样和使用适当的表型和遗传标记物的重要性受到压力,并且关于BMI(体重指数)的研究的一个例子,显示位于染色体7的主要遗传因子的作用示出了一些上述策略。建议将来,尽管认识到多重家族仍将是连锁研究的主要和有效类型的采样(例如,利用汇集的DNA样品的采样类型(例如不相关的控制)将普遍采用。识别研究与其解释之间的遗传异质性将是即将到来的复杂性状研究中的突出特征之一。

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