SNV:单核苷酸变异
“单核苷酸变异”(Single Nucleotide Variation)常缩写为SNV,这种简写形式便于书写和使用,广泛出现在生物信息学、遗传学及医学研究等综合领域。该术语用于描述基因组中单个核苷酸发生的变异,是遗传变异研究中的常见类型之一。
Single Nucleotide Variation具体释义
Single Nucleotide Variation的英文发音
例句
- Relationship between single nucleotide variation in mitochondrial DNA D-Loop region and PCOS
- 线粒体基因D-Loop区单核苷酸变异(SNV)与多囊卵巢综合征的相关性研究
- Study and Application of Single Nucleotide Polymorphism in Chicken Genetic Variation
- 单核苷酸多态性技术在鸡遗传变异中的研究及应用
- Moreover, Many pathogenic and genetic diseases are associated with changes in the sequence of particular genes. Among these changes, the point mutation, i.e. single nucleotide polymorphisms ( SNPs ), are the most abundant form of genetic variation.
- 此外,人类的许多遗传性疾病都是由于基因的变异引起的,其中尤以单碱基的突变,即单碱基多态性最为普遍。
- Single nucleotide polymorphism ( SNP ) & A polymorphism in DNA sequence consisting of variation in a single base.
- 由单个基因发生突变引起的遗传病。
- Extremely abundant molecular polymorphisms such as single nucleotide polymorphisms ( SNP ) and complete genome sequences in model organisms will greatly advance accurately genetic dissection for quantitative trait variation.
- 基因组上数以万计的DNA序列变异(例如SNP)以及模式生物全基因组测序的完成,已为这种准确的遗传剖分提供了必要的条件。
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