Phenograms were constructed by using genetic distance UPGMA method.
用距离系数upgma法聚类分析产生了树状图。
The two analyses show the UPGMA tree is accord with the relationship of the cultivars.
两次分析说明聚类的树状图和品种间亲缘关系的一致性。
Based on the ISSR band data, similarity indices and UPGMA dendrogram were analysed and developed.
基于ISSR条带统计数据，运用相关软件进行了相似系数的分析和系统进化树的构建。
UPGMA is taken to calculate the genetic distance within and between populations. Systematic tree is constructed.
应用UPGMA法计算了种群内和种群间的遗传距离，并构建了系统树。
The systematic diagram of genetic relationships was established by POPGENE32 software and clustered by UPGMA method.
利用POPGENE32软件分析遗传相似系数，UPGMA方法聚类，构建亲缘关系系统图。
UPGMA cluster analysis showed that natural populations and cultivated populations were distinctly separated into two groups.
UPGMA聚类分析表明自然居群与栽培居群存在明显的分化而分别聚为两大类群。
Compared with other systematic clustering method, UPGMA would be better for the numerical taxonomy of the capsicum varieties.
比较不同的系统聚类方法，类平均法能较好适合辣椒品种的数量分类。
The results of PCA and UPGMA clustering analysis exhibited a good consistency, and were also consistent with geographic origins.
主坐标和UPGMA聚类分析结果基本相同，并与地理来源有很高的一致性。
The results of cluster analysis by using UPGMA method showed that all the tested accessions could be differentiated by RAPD marks.
聚类分析结果表明利用RAPD技术可将全部供试材料区分开。
These 6 tea lines were divided into 2 groups by UPGMA, moreover, the 4th line was proved to be pollen plant on DNA molecular level.
进行聚类分析，将6个株系划分为两个类群，并在DNA分子水平上进一步证实株系4为花粉植株。
And according to the genetic similarity coefficient, the genetic relationship among these local varieties was researched by UPGMA method.
并基于遗传相似系数、采用UPGMA法对这些地方品种的遗传关系进行了研究。
UPGMA cluster analysis based on two molecular markers data divided these melons into two groups: wild melon group and cultivated melon group.
根据两种标记的结果，采用UPGMA聚类分析，将供试材料分为两大类群：野生甜瓜和栽培甜瓜；
According to the data of RAPD and ISSR molecular markers of the leaf samples, UPGMA cluster was made at population level and individual level.
分别依据古银杏叶片样品的RAPD和ISSR标记数据，进行了群体和单株聚类分析。
Genetic similarities were calculated using simple matching coefficient, and the phenogram was constructed by using UPGMA method. Three cultivars of n.
计算各样本间的相似性系数和遗传距离，并采用UPGMA法对遗传距离进行了聚类分析。
Molecular phylogenetic tree constructed by UPGMA and NJ method suggested that there were some genetic variation among different geographic population.
UPGMA和NJ法构建的种群间分子系统树基本一致，结果表明不同地理种群之间存在一定程度的遗传差异。
The result showed that the DNA fingerprints similarity coefficient between basidiocarps and their mycelia were 1.00 by constructing the UPGMA tree chart.
结果表明：松口蘑子实体与分离物的DNA指纹相似系数为1.00，进而断定分离物为松口蘑菌丝体。
For UPGMA cluster analysis, 12 Oryza species were classified into three cluster groups with the similarity coefficient of 0.696 using the software NTSYS.
利用NTSYS进行UPGMA聚类分析后，发现这12种材料在遗传相似系数0.696为阀值处可以分为3个类群。
Genetic distances of each pair of lines are calculated by Nei's method. The results of cluster by method UPGMA show that the population has less over presentation.
对各株系间的根井遗传距离采用UPGMA法对群体进行聚类分析表明群体中很少存在代表性重复现象。
In this paper, based on average Eucli dean distance coefficient, using UPGMA, Q cluster analysis for karyotype of 12taxa in genes glycyrrhiza L. have been conducted.
在平均欧氏距离系数基础上，运用UPGMA法，对甘草属12个类群的核型资料进行了Q型聚类分析。
These samples were divided into two groups according to its breeding source using UPGMA method. Moreover, the genetic structure of two sets of varieties is different.
聚类结果表明两套品种（系）各自聚为一类，遗传结构分析也显示两套品种（系）之间存在明显的差异。
Both UPGMA cluster and PCA analysis showed clear genetic relationships between the 24 mulberry cultivars. The major clusters were related to known pedigree relationships.
UPGMA法聚类和PCA分析都清楚地显示了24个桑树选育品种的亲缘关系，聚类结果与桑树品种的系谱基本一致。
Using unweighted pair group method with arithmetic average (UPGMA), 9 populations of Emmenopterys henryi were clustered into two groups, inner-province group and outer-province group.
利用算术加权平均数法（UPGMA）对香果树居群进行聚类，结果9个居群可分成浙江省内和省外两大类群。
In order to identify enzyme systems related to some traits of Chinese plum, we used 2 enzyme systems for individual UPGMA cluster analysis. But their collection remains to be investigated.
用2种酶系统分别对中国李进行单株聚类分析，中国李某些性状与等位酶基因位点或等位基因的相关性有待进一步研究。
Cluster analysis of DGGE by UPGMA and NMDS analysis suggested that microbial structures in two reactors did not evolve in the same direction obviously although they worked in the same system.
UPGMA聚类分析和NMDS散点分析表明，水解、好氧反应器内的微生物并没有因为同处一个系统内而使得其菌群落结构产生明显的趋同倾向。
Cluster analysis of DGGE by UPGMA and NMDS analysis suggested that microbial structures in two reactors did not evolve in the same direction obviously although they worked in the same system.
UPGMA聚类分析和NMDS散点分析表明，水解、好氧反应器内的微生物并没有因为同处一个系统内而使得其菌群落结构产生明显的趋同倾向。
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