Suppr超能文献

[乌兹别克斯坦血红蛋白病的群体遗传学研究。II. 血红蛋白病的群体动态]

[Population genetics study of hemoglobinopathies in Uzbekistan. II. Population dynamics of hemoglobinopathies].

作者信息

Asanov A Iu, Ginter E K, Bakhramov S M, Gar'kavtseva R F, Revazov A A

出版信息

Genetika. 1987 Jul;23(7):1328-33.

PMID:2958388
Abstract

It was shown that on comparing variability of selective neutral genetic marker systems with that of the beta-thalassemia system for the populations of different hierarchical level, the relative importance of selection and genetic drift could be evaluated. The genetic differentiation of the beta-thalassemia gene frequencies in elementary populations (villages) could be solely explained by genetic drift. On the other hand, the differentiation of district populations (the sizes of the populations being 10(6] for beta-thalassemia gene frequencies could be explained by selection forces. This is supported by the fact that the genetic distances and FST values are only significant for the beta-thalassemia gene and not for the neutral genetic systems, when the district populations are compared.

摘要

结果表明,在比较不同层次水平人群的选择性中性遗传标记系统和β地中海贫血系统的变异性时,可以评估选择和遗传漂变的相对重要性。基层人群(村庄)中β地中海贫血基因频率的遗传分化完全可以用遗传漂变来解释。另一方面,地区人群(人群规模为10^6)中β地中海贫血基因频率的分化可以用选择力来解释。当比较地区人群时,遗传距离和FST值仅对β地中海贫血基因有显著意义,而对中性遗传系统没有显著意义,这一事实支持了这一点。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验