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1)  splice site mutation
剪接位点突变
2)  splice mutation
剪接突变
1.
Identification of a novel splice mutation of low density lipoprotein receptor gene in a Chinese family with familial hypercholesterolemia;
家族性高胆固醇血症家系低密度脂蛋白受体基因剪接突变的研究
3)  splice site
剪接位点
1.
Identification of splice sites based on feature mining and integration;
基于特征挖掘与融合的剪接位点识别
2.
Splice Site Identification Based on Hidden Markov Support Vector Machines;
基于HM-SVM的剪接位点识别
3.
Eukaryotic DNA Splice Site Identification Based on the Machine Learning Approach;
基于机器学习方法的基因剪接位点识别研究
4)  splice sites
剪接位点
1.
Application of Takagi-Sugeno model in the recognition of splice sites;
Takagi-Sugeno模型在剪接位点识别中的应用
2.
Rough set-genetic algorithms-k-nearest neighbor and its application in DNA sequence splice sites recognition;
RS-GA-KNN算法识别灵长类动物DNA序列剪接位点
3.
Experimental results show that HMM is good at retrieving the statistical characteristics of consensus sequences around splice sites and the recognition rat.
隐Markov模型(Hidden Markov model,HMM)用于基因识别研究是生物信息学研究的新领域,剪接位点的识别是基因识别中的一个重要环节。
5)  splicing sites
剪接位点
1.
Secondary structural characteristic of eukaryotic gene splicing sites;
真核基因剪接位点二级结构特征
2.
Application of hidden Markov model in the recognition of splicing sites;
隐Markov模型在剪接位点识别中的应用
6)  splicing variant
剪接突变体
1.
Results A novel mRNA splicing variant of EOLA1 was identified with 19 redundant base pairs at the beginning of the 3rd exon of the target sequence published in Genebank.
结果 测序发现一种目的基因mRNA剪接突变体 ,其第 3外显子起始部分比Genebank数据库相应序列多出 19个碱基。
补充资料:多位点突变发生
分子式:
CAS号:

性质:在遗传物质中发生两个或多个相邻核苷酸改变的突变,包括核苷酸的置换或缺失。

说明:补充资料仅用于学习参考,请勿用于其它任何用途。
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