The multi-primer RAPD analysis is an excellent method in typing Pseudomonas aeruginosa.
多种引物RAPD分析是判断铜绿假单胞菌流行情况的有利工具。
RAPD analysis was made with the cpDNA as template and clear amplification profile was obtained.
用所提取的叶绿体dna作为模板进行RAPD扩增，获得了清晰的扩增图谱。
Conclusion CTAB Method and RAPD reaction system can be used to RAPD analysis in Rhizoma Coptidus.
结论CTAB法及黄连药材的RAPD反应体系可以用于黄连药材的RAPD分析。
Our results showed that RAPD correction can improve the reproducibility of RAPD analysis significantly.
结果表明，RAPD校正能显著地提高RAPD扩增的重复性。
Objective to excogitate a method for extracting DNA from Bulbus Lilii to be appropriate for RAPD analysis.
目的建立一种适合RAPD分析的百合鳞叶总DNA提取方法。
Optimizing condition of RAPD improved veracity and repetition of RAPD anaLysis, and insured reaLity and nicety.
并对RAPD反应的条件进行了优化，提高RAPD分析的可靠性和重复性。
RAPD analysis will provide a new path for identification and classification of ancient litchi genetic resources.
应用RAPD技术为荔枝古树遗传资源的鉴定和分类提供了新的途径。
The thesis selected 4 effectives primer from 50 random primers produced by Shanghai Sangon Company in RAPD analysis.
RAPD分析中，应用了上海生工s系列的50个随机引物中筛选出的4个有效引物。
Plantlets were subjected to RAPD analysis, and the result of RAPD showed that regenerants from calli had a higher genetic variation.
再生的植株经rapd分析表明，经过愈伤组织再生的植株遗传变异性较高。
Using this program, experimental time is reduced, while PARD patterns are not changed, thus, it increases efficiency of RAPD analysis.
采用这一方案，缩短了实验时间而保持RAPD图谱不变，因而提高了RAPD分析的效率。
Two PCR amplified fragments were found to be tightly linked to Pi-h-1 (t) by RAPD analysis. of near isogenic pools of DNA from F2 plants.
应用近等基因池DNA和随机引物，经PCR扩增和共分离分析，建立了二个RAPD片段与抗病基因紧密连锁。
RAPD analysis had high distinguish ability and could provide more direct, rich and precise genetic information than plasmid profile analysis.
相对于质粒分析而言，RAPD分析具有更高的分辨率，它提供的遗传学信息更为丰富、直接、精细。
RAPD analysis of genetic diversity would be useful in cross combination setting of breeding for high resistance to stem-nematode in sweetpotato.
遗传多态性的RAPD分析可为甘薯抗茎线虫病品种选育的亲本组配提供依据。
Qualified DNA could be obtained from Litsea coreana var. lanuginose by means of the improved SDS method. The DNAs are qualified for RAPD analysis.
结果表明，采用改良SDS法从毛豹皮樟的老、幼叶片中都能提取到高质量的DNA，可以用于RAPD分析；
However, the two main morphological characters of blooming time and the color of inside perianth are not supported by the results of RAPD analysis.
花期与内被片颜色这两个主要的形态学分类性状，未得到RAPD分析结果的支持。
Genetic distance among different populations are 0~0.016, which is belong to infraspecies genetic variation, this result is consistent with RAPD analysis.
各地理种群间的遗传距离为0～0.016，表现为种下的遗传变异，这与RAPD分析得出的结果相一致。
However, the RAPD analysis provides a more informative result in terms of the overall genetic relationships at the species level compared to the SSR analysis.
然而，涉及到品种间全部的遗传关系，RAPD分析比ssr提供了更多的信息量。
Quail lines selected for high and low stress in Department of Poultry Science, LSU, USA were fingerprinted by RAPD analysis of genomic DNA to evaluate genetic polymorphism.
本研究对美国路易斯安那州立大学家禽系选育的高应激和低应激两个品系鹌鹑进行RAPD分析，评定其遗传多态性。
Differences were found among 8 strains from RAPD analysis. Out of 23 random primers, 11 were polymorphic. Altogether 59 RAPD bands were found and the polymorphic rate was 47.5%.
应用23个随机引物对白粉病菌8个不同生理小种进行RAPD分析，其中11个引物的扩增带型在不同生理小种间出现差异，共扩增出59条谱带，多态性为47.5%。
METHODS The genes of imipenem-resistant P. aeruginosa were amplified by RAPD assay in 8 clinical isolates and PCR products were analyzed by agarose gel electrophoresis and cluster analysis.
方法对医院临床分离的8株耐亚胺培南铜绿假单胞菌进行随机引物聚合酶链反应（PCR）扩增，扩增产物进行电泳和聚类分析。
The identification and genetic analysis of 8 oil sunflower inbred lines were carried out by using RAPD markers.
利用RAPD标记对8个油用向日葵自交系进行了鉴定和遗传分析。
Methods Polymorphic analysis was used for the commercial crude drug Bulbus Lilii with RAPD technique and a tree diagram was constructed.
方法采用RAPD技术对商品药材百合进行了多态性分析，并构建聚类树型图。
The cluster analysis for RAPD markers were made and it was found that the result could be preliminarily classified by parts of botanic characters.
通过对RAPD扩增位点进行聚类分析，发现以部分植物学性状等背景资料能对聚类结果进行初步的分类，并给予一定合理的解释。
The random amplified polymorphic DNA(RAPD) technique was applied to the genetic analysis of Xingguo red carp (Cyprinus carpio var.
运用随机扩增多态DNA方法对兴国红鲤、苏联镜鲤、德国镜鲤及它们的杂交后代进行遗传分析。
Using this program, experimental time is reduced, while RAPD patterns is not changed, thus, it increases efficiency of RAPD-analysis.
采用这一方案，缩短了实验时间而保持RAPD图谱不变，因而提高了RAPD分析的效率。
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。
SSR can be expected to complement existing RFLP, RAPD, AFLP maps, and are useful for genotype identification. gene and QTL analysis, marker assisted selection in breeding and pedigree analysis.
林木的微卫星标记可扩充现有的RFLP、RAPD、AFLP遗传图谱，以及QTL分析，并应用于基因型鉴别，分子标记辅助选择育种。
In this experiment, we chose 16 pomegranate cultivars as the experimental materials, and selected 10 RAPD primers with good reproducibility and polymorphism for analysis.
本实验以16个石榴品种为实验材料，筛选出10个重复性及多态性均较好的引物进行RAPD分析。
Said disease-resisting translocation line Y96060 can be confirmed by means of cytogenetic analysis, chromosome C zoning and in situ hybridization and RAPD technique.
抗病易位系Y96060可通过细胞遗传分析，染色体C分带和原位杂交技术，RAPD技术得到确认。
Said disease-resisting translocation line Y96060 can be confirmed by means of cytogenetic analysis, chromosome C zoning and in situ hybridization and RAPD technique.
抗病易位系Y96060可通过细胞遗传分析，染色体C分带和原位杂交技术，RAPD技术得到确认。
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