base deletion 碱基缺失 ; 碱基删除
single-base deletion 单碱基缺失
single-base deletion mutation 单碱基缺失突变
base pair deletion 碱基缺失
A single base G deletion 单碱基G缺失
By using Genedoc to compare the sequences of these 20 individuals, 54 variation sites were observed, of which 2 are of base deletion, 1 base insertion, 43 transition sites, 7 transversion sites and 2 transition-transversion sites.
用Genedoc软件进行序列比较,在这20个个体中,共检测到54个变异位点,包括:2个碱基缺失、1个碱基插入、43个转换位点、7个颠换位点及2个转换与颠换同时存在的位点。
参考来源 - 蓝点马鲛和日本鳀的遗传多样性研究·2,447,543篇论文数据,部分数据来源于NoteExpress
The results show that the types of DNA base mutation included the transition, the transversion and the deletion.
结果显示:碱基变异的类型包括转换、颠换和缺失。
In all of the 24 bases of mutants, the base replacement occupies about 87.5% of the total mutants with only a small portion of gene deletion (12.5%).
在检测到的24个碱基突变中,主要是碱基的置换(87.5%),碱基缺失的比例比较小(12.5%)。
Finally, some base functions come to realize such as addition of the data, modification, deletion and so on, also integrates the database with MEMS GARDEN3. 0.
最后,实现了数据库数据的增加、修改、删除等功能,并且有效的与实验室平台(MEMS GARDEN3.0)进行集成。
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