Molecular cloning and sequence analysis were performed.
并进行分子克隆和测序分析。
The sequence analysis is a two-stage process for sequential pattern mining 1.
顺序分析是一个两阶段的顺序模式挖掘流程1。
DNA, complementary; cloning, molecular; sequence analysis; gene expression.
互补；克隆分子；序列分析；基因表达。
Dynamic programming is an algorithmic technique used commonly in sequence analysis.
动态编程是在序列分析中经常使用的一种算法技术。
Sequence analysis showed that homology of nucleotide and amino acid of ts was high.
核苷酸序列与氨基酸同源性分析表明该片段较为保守。
Biological sequence analysis is an important application domain of data mining technology.
生物序列分析是机器学习和数据挖掘技术一个重要的应用领域。
For sequence analysis, fragments of 100 ~ 200 nucleotides in length were eluted from the gel.
从制备胶上洗脱长度在100 ~ 200个核苷酸的片段供顺序分析。
Sequence analysis revealed sequence differences of 1-3 nucleotides involving three separate codons.
核苷酸顺序分析表明存在1—3个核苷酸取代。
Sequence analysis showed that it contained the basic characteristic of primary structure of promoter.
对其序列分析表明它具有启动子初级结构的基本特征。
Sequence analysis showed the amplified fragment was the TIV1 fragment of the vacuolar invertase gene.
测序结果表明，所获得的片段为番茄液泡转化酶基因TIV1的片段；
Sequence analysis result indicated GP had a glycosylation site at position 319 and whole antigenic sites.
分析它的主要功能位点表明它具有319位的糖基化位点和完整的抗原位点。
After sequence analysis, RT PCR method was used to analyze the expression pattern in human fetal tissues.
序列分析后用RTPCR方法研究胎儿组织中的表达情况。
It should assist in the future nucleic acid sequence analysis and novel gene identification in this region.
这项研究为这一区域进一步进行核苷酸顺序分析和该区域的功能和疾病基因克隆奠定了基础。
Sequence analysis of the randomly picked 96 Ig clones showed the library contains various antibody gene types.
对随机挑取的96个克隆测序序列分析表明各种型别比例基本合适；
A novel method for the radar full pulse data analysis, called the extremum sequence analysis method, is put forward.
针对脉冲雷达提出了一种新的雷达信号全脉冲数据分析算法？极值序列分析法。
A novel method for radar signal full pulse data analysis, called the extremum sequence analysis method, is put forward.
针对脉冲雷达提出了一种新的雷达信号全脉冲数据分析算法——极值序列分析法。
It differs from traditional time-sequence analysis methods in which nonlinear chaotic time-sequence prediction is used.
采用非线性混沌时间序列预报，不同于传统的时间序列分析方法。
The sequence analysis results provided a important basis for further study of the APP colonization and virulence factors.
比对的结果为寻找研究APP的定植基序和毒力因素提供了重要基础。
It can be used in the discovery of non-redundant association rules, sequence analysis, and many other data mining problems.
它可以进一步应用到无冗余关联规则发现、序列分析等许多数据挖掘问题。
Methods The BO mutants I402G and C457S were obtained by site-directed mutagenesis and confirmed by amino acid sequence analysis.
方法胆红素氧化酶突变体i 402g和C457S通过聚合酶链反应获得，并经氨基酸序列测定加以证实。
ResultsThe results of genotyping in two-step PCR-CTPP were consistent with those conducted by PCR-RFLP and DNA sequence analysis.
结果通过两步法PCR-CTPP得到的基因分型结果与PCR-RFLP和DNA测序得到的基因分型结果完全一致。
The general principles and methodology of genetic stratigraphic sequence analysis using well log data are discussed in this paper.
本文主要讨论利用测井资料进行成因地层层序分析的一般原则与方法。
Sequence analysis showed high similarity (up to 98.9%) between fungal BAPT gene fragments and the counterparts from their yew hosts.
序列分析表明，来自内生真菌的BAPT基因片段序列与红豆杉BAPT基因片段序列具有非常高的相似性(98.9%)。
COI genes of hookworm was amplified from hookworm genomic DNA by PCR and sequenced. Program MEGA was used for the sequence analysis.
采集安徽和四川两省的十二指肠钩虫，用PCR技术扩增COI基因，同时测序并用MEGA软件进行遗传差异的分析。
Single strand conformation polymorphism (SSCP) essay and sequence analysis of the PCR product were used to ascertain the gene mutation.
方法应用PCR及单链构象多态性(SSCP)分析技术结合基因序列测定方法确定突变类型。
The results of agarose gel electrophoresis and DNA sequence analysis indicated that the PCR method had high specificity and sensitivity.
结果经琼脂糖凝胶电泳和DNA序列测定证实，建立的PCR检测方法具有极高的灵敏度和较好的特异性。
Sequence analysis showed that its nucleotide sequence had high identity to a Japanese isolate of RDV and contained high percent of rare codons.
序列分析表明该基因与日本株具有高度同源性，并且含有较高比例的稀有密码子。
Sequence analysis showed that its nucleotide sequence had high identity to a Japanese isolate of RDV and contained high percent of rare codons.
序列分析表明该基因与日本株具有高度同源性，并且含有较高比例的稀有密码子。
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