Allele frequencies for all loci were determined directly by counting. 的简体中文翻译

Allele frequencies for all loci wer

Allele frequencies for all loci were determined directly by counting. Unbiased estimates of gene diversity (expected heterozygosity) with associated standard errors were computed for all locus/population combinations according to Nei (1987). The mean number of alleles per locus (MNA) was also calculated as an index of sample diversity. A size-adjusted MNA value was calculated using 1000 iterations of a resampling method.B. taurus-associated alleles were selected by comparing pooled European breed data with pooled data from all Indian samples. A scaled frequency differential (SFD) was calculated for each allele by the formulawhere PE is the average frequency of the allele in the 11 European breeds and PI is the average frequency in the seven Indian breeds assayed. The higher of these two values is denoted by the denominator. This SFD measure was combined with other criteria to define three categories of PAAs, each a subset of the previous. Initially, zebu alleles were defined as those that are at higher frequency in the Indian population than in the European population, and taurine alleles are the converse. Category I PAAs include both zebu and taurine alleles that have a frequency of greater than 5% in the respective parental population. Alleles with a frequency lower than this were removed from the analysis. Category II PAAs are the subset of category I, which are taurine alleles, that is, those found at higher frequency within B. taurus populations. Category III PAAs are a more stringent selection of taurine-associated alleles and are those found at a frequency of at least 20% in European populations and an SFD of greater than 40%. The average frequencies of categories II and III PAAs were calculated for each breed and these values were used as measures of B. taurus admixture.
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所有基因座的等位基因频率通过计数直接确定。根据 Nei (1987) 计算所有基因座/群体组合的基因多样性(预期杂合性)的无偏估计和相关标准误差。每个基因座的平均等位基因数 (MNA) 也被计算为样本多样性的指标。使用重采样方法的 1000 次迭代计算大小调整后的 MNA 值。<br><br>通过比较汇集的欧洲品种数据与来自所有印度样本的汇集数据来选择 B. taurus 相关等位基因。通过以下公式计算每个等位基因的比例频率差 (SFD)<br><br><br>其中 PE 是 11 个欧洲品种的等位基因的平均频率,PI 是所分析的 7 个印度品种的平均频率。这两个值中较高的值用分母表示。该 SFD 衡量标准与其他标准相结合,定义了三类 PAA,每类都是前一类的子集。最初,瘤牛等位基因被定义为在印度人群中的频率高于欧洲人群,而牛磺酸等位基因则相反。I 类 PAA 包括瘤牛和牛磺酸等位基因,它们在各自的父母群体中的频率大于 5%。从分析中去除频率低于此频率的等位基因。II 类 PAA 是 I 类的子集,它们是牛磺酸等位基因,即在 B. taurus 种群中以较高频率发现的那些。III 类 PAA 是对牛磺酸相关等位基因的更严格选择,在欧洲人群中发现的频率至少为 20%,SFD 大于 40%。计算了每个品种的 II 类和 III 类 PAA 的平均频率,并将这些值用作 B. taurus 混合物的量度。
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结果 (简体中文) 2:[复制]
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所有基因座的等位基因频率直接通过计数确定。根据Nei(1987),对所有位点/群体组合的基因多样性(预期杂合度)进行无偏估计,并计算相关标准误差。每个位点的平均等位基因数(MNA)也被计算为样本多样性的指标。使用重采样方法的1000次迭代计算尺寸调整后的MNA值。<br>金牛座相关等位基因是通过比较欧洲品种数据和所有印度样本的数据来选择的。通过公式计算每个等位基因的比例频率差(SFD)<br>其中,PE是11个欧洲品种中等位基因的平均频率,PI是所分析的7个印度品种中的平均频率。这两个值中的较高值由分母表示。该SFD度量与其他标准相结合,定义了三类PAA,每一类都是前一类的子集。最初,zebu等位基因被定义为在印度人群中的频率高于在欧洲人群中的频率,而牛磺酸等位基因则相反。I类PAA包括zebu和牛磺酸等位基因,它们在各自的亲本群体中的频率大于5%。频率低于此值的等位基因从分析中删除。II类PAA是I类的子集,I类是牛磺酸等位基因,即在金牛双歧杆菌群体中发现的频率较高的基因。III类PAA是牛磺酸相关等位基因的更严格选择,在欧洲人群中发现的频率至少为20%,SFD大于40%。计算每个品种II类和III类PAA的平均频率,并将这些值用作衡量金牛双歧杆菌混合的指标。
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结果 (简体中文) 3:[复制]
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