最新的一份报道泰国对猪流感病毒采用分子和系统进化分析法分析。
The present report presents molecular and phylogenetic analysis performed on SIV in Thailand.
分子进化分析发现，同属的微孢子虫可以处于系统进化树不同的分枝。
Molecular evolution analysis indicated that the microsporidia which even belonged to same genus could be classified to different branch.
进化分析的结果显示，文昌鱼的肌动蛋白基因家族可能通过串联重复而发生了扩增。
Phylogenetic analysis suggests the amphioxus actin genes have clearly undergone extensive expansion through tandem duplications.
对分离到的HEV71阳性分离株进行VP1编码区基因扩增，核苷酸序列测定和同源进化分析。
And identified HEV71 isolates were performed by gene amplification of VP1 coding region, nucleotide sequencing and homology analysis of evolution.
分子进化分析表明，22个BADH基因由同一基因进化成五个类群，双子叶植物进化变异较大；
The phylogenetic analysis from 22 kinds of plant BADHs indicated the larger variability in the dicotyledonous plants, one group in the Gramineae plants including BADH genes form E.
尽管信号传导因子的序列分化较大，但系统进化分析显示它们在不同昆虫间呈明显的直系同源关系。
Phylogenetic analysis showed that the signal transducers have remarkable orthologous relationships between different insect species in spite of the divergent sequences.
通过序列同源比对及系统发育进化分析，发现克隆到的序列与其它物种DOB基因具有很高的同源性。
Sequence of SLA-DOB1 was cloned that was high homology with the other species by multiple sequences alignment and phylogeny evolution analysis.
对5个基因间的两两比较分析和进化分析结果表明：该基因簇是通过一系列的串联基因复制事件而形成；
Comparative analysis and evolutionary analysis of the clustered genes and other peroxidase family members revealed that the gene cluster occurred by tandemly gene duplications(from osp5 to osp1 );
多序列比对是一种重要的生物信息学工具，在生物的进化分析以及蛋白质的结构预测方面有著重要的应用。
Multiple sequence alignment is one of the essential tools of studying bioinformatics and it plays an important role in the evolution analysis and protein structure prediction.
比较基于该区段及基于基因组全序列进行的系统进化分析结果，进一步证明该区段可替代全序列用于基因分型。
Phylogenetic analysis results are compared based on the full length and the selected region to further prove the statistical results.
系统进化分析显示，5组蜱和土拉菌聚在一个分支上，其余8组和弗朗西斯菌属（类）内共生体聚在一个主干分支上。
The phylogenetic analysis indicated that 5 groups were assigned to a clade of F. tularensis, and the rest 8 groups to main clade with FLEs.
方法设计特异的PCR引物，用RT-PCR技术分段扩增Q32株全长L、M片段，PCR产物纯化后直接测序，或用T-A克隆方法进行PCR产物克隆，然后进行遗传进化分析。
Methods The L and M segment cDNA of Hantavirus Q32 strain was amplified by RT-PCR. The purified PCR products were sequenced directly or cloned into pGEM-T Vector and then sequenced.
方法设计特异的PCR引物，用RT-PCR技术分段扩增Q32株全长L、M片段，PCR产物纯化后直接测序，或用T-A克隆方法进行PCR产物克隆，然后进行遗传进化分析。
Methods The L and M segment cDNA of Hantavirus Q32 strain was amplified by RT-PCR. The purified PCR products were sequenced directly or cloned into pGEM-T Vector and then sequenced.
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