1) Shannon's index
多态位点率
2) percentage of polymorphic loci
多态位点百分率
1.
The percentage of polymorphic loci(P)ranging from 79.
6个群体均具有丰富的遗传多样性,多态位点百分率为79。
3) polymorphic loci
多态位点
1.
Results:The proportion of polymorphic loci,mean expected hetrozygosities and Shannon s index of the suzhou population were 25%,0.
结果:苏州养殖种群的多态位点比例为25%,种群平均杂合度为0。
2.
The proportion of polymorphic loci,mean expected heterozygosity and Shannon\'s index of the Heihe River population were 25.
结果表明,黑河种群的多态位点比例(P)为25。
4) polymorphism
[英][,pɔli'mɔ:fizəm] [美][,pɑlɪ'mɔrfɪzṃ]
多态性位点
1.
With the development of several technologies,such as large-scale genome sequencing,gene chips and mass spectrometry,and the successful completion of the first phase of International HapMap Project,it is feasible to explore the associations between hundreds of polymorphisms in the human genome,even the whole genome,and complex diseases in populations with large number of samples.
确定影响复杂疾病的遗传因素是一个相对困难的问题,随着大规模基因组测序技术、基因芯片和质谱技术等高通量技术的发展,以及国际人类基因组单体型图计划(HapMap)第一阶段的成功完成,在大规模人群中研究成百乃至全基因组的多态性位点与复杂疾病的关系成为可能。
2.
Objective:To study the allele frequencies of Parkin polymorphism S/N167,R/W366 and V/L380 at exon 4 and exon 10 in the patients with Parkinson disease in Guangxi and analyze the association between the allele frequencies of Parkin polymorphism and the etiology in the disease.
目的:研究Parkin基因4、10号外显子多态性位点S/N167、R/W366、V/L380等位基因频率与广西地区帕金森病发病的关系。
5) SNP
[英][,es en 'pi:] [美]['ɛs 'ɛn 'pi]
多态性位点
1.
Identification of characteristics single nucleotide polymorphisms (SNPs) existing in coding region of the gene, CYP4A11, may provide some new insights into the genetic mechanisms of hypertension.
寻找人群中该酶基因之一的CYP4A11的编码区多态性位点分布情况,可以为研究高血压病的基因机制提供新的依据。
2.
AIM:To identify the characteristic single nucleotide polymorphisms(SNPs)existing in the coding region of arachidonic acid ω-hydroxylase gene,CYP4F2,in a Han population.
目的寻找汉族人群花生四烯酸细胞色素P450ω-羟化酶基因CYP4F2的编码区多态性位点分布情况。
6) Polymorphic Point
多态性位点
1.
An Analysis of A Possible Polymorphic Point of PLAG1in Chinese;
中国汉族人多形性腺瘤基因1多态性位点分析
2.
An analysis of two polymorphic points of the 7th intron of human p53 gene;
p53基因第7内含子序列的多态性位点分析
补充资料：多克隆位点
分子式：
CAS号：
性质：在所使用的载体插入外源片段的位置，加上一段人工合成的寡聚脱氧核糖核酸(ONT)，这段ONT由一连串的预设的限制性内切酶切点组成，每一切点之间的碱基数是3的倍数，这样插入不同酶切位点都不会引起推移。
CAS号：
性质：在所使用的载体插入外源片段的位置，加上一段人工合成的寡聚脱氧核糖核酸(ONT)，这段ONT由一连串的预设的限制性内切酶切点组成，每一切点之间的碱基数是3的倍数，这样插入不同酶切位点都不会引起推移。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条