基本释义:

突变常数

网络释义

1)mutation constant,突变常数

2)abnormal sudden change,异常突变

3)Abrupt anomaly,突变异常

4)accidental data,突变数据

5)catastrophe theory,突变级数

6)breaking factor,突变系数

用法和例句

This method can reduce the deviations with are made by the accidental data.

文章着重讨论了在实际评估中,对于突变数据采用一种非线性偏差补偿方法,通过历史数据分析,构造出一种补偿模型,用于调整权值系数,从而达到抑制突变数据对整个评估结果造成的偏差。

The article introduces four types of catastrophe theory, based on grey theory and Fuzzy maths, a model of multistage catastrophe evaluation is built up.

利用突变级数法的基本思想和突变系统的4种常用类型:尖点突变、燕尾突变、蝴蝶突变、因第安人茅舍突变,依据灰色理论和模糊数学,建立多目标的突变评价方法模型。

The article introduces three types of catastrophe theory, based on credit evaluation grading index system of listed corporation, we evaluate ten listed corporations, and obtained better result of evaluating.

利用突变级数的基本思想和突变系统的三种常用类型 :尖点突变、燕尾突变、蝴蝶突变 ,在建立上市公司资信评估指标体系的基础上 ,应用三种突变类型对 1 0个公司的资信程度进行了综合分析 ,得到较好的评价结

A new segment method based on the properties of temporal data is proposed,which pided temporal data by combining important point with their breaking factor(BF).

因此,提出从时序数据自身特点出发,得到突变系数和重要点,依据重要点和突变系数的新的划分方法,并以微软的股票数据进行测试。

Study on the Causes of Anormalous Water Level Changes in Huoshan 33 Well,Anhui Province

霍山皖33井水位突变异常成因的研究

To mutate or change morphologically, often reversibly.

突变，变异经受突变或形态上的改变，常为可逆地

Changes of α-synuclein After Accumulation

α-突触核蛋白异常沉积后的成分改变

The Mutations and Protein Expressions of PTEN and p53 Genes in Malignant Transformation of Endometriosis

PTEN和p53基因突变和蛋白异常表达与子宫内膜异位症恶变的关系

Müllerian anomalies,hearing loss,and connexin 26 mutations

苗勒管发育异常、听力丧失与连接蛋白26突变

Identification of Novel Mutations in the ADAR Gene of Dyschromatosis Symmetrica Hereditaria (DSH)

遗传性对称性色素异常症基因新突变的发现

Study on the Mutations of ADAR1 Gene in the Patients with Dyschromatosis Symmetrica Hereditaria;

遗传性对称性色素异常症致病基因突变研究

Study of Mutations on the D-Loop Region of Mitochondrial DNA in Myelodysplastic Syndrome;

骨髓增生异常综合征线粒体DNA D-loop区突变研究

Mutation of Two Families with Dyschromatosis Symmetrical Hereditaria

遗传性对称性色素异常症家系的DSRAD基因突变

Most of an inpidual's genes, however, are inherently good.

然而人类个体的基因生来就是正常的，很少发生突变（变异）。

Even in these days of rapid technological change, the abruptness of this transition was unusual.

即使在目前技术日新月异的时代，这个转变的突然性也是不寻常的。

Mutation Identification and Functional Analysis of ADAR, the Disease Gene for Dyschromatosis Symmetrica Hereditaria

遗传性对称性色素异常症致病基因的突变鉴定和功能分析

Its gravitational field is on a density suddenchange belt of Bouguer anomaly isopleth.

重力场则处于布伽重力异常等值线疏密突变带上。

Localization of DSH-associated Gene and Identification of the Gene Mutation;

遗传性对称性色素异常症致病基因的定位和突变研究

Mutations in the D-LOOP Region of Mitochondrial DNA in Myelodysplastic Syndrome;

骨髓增生异常综合征线粒体DNA D-LOOP区突变的研究

Study on Mitochondria Cytochrome Oxidase (CO Ⅰ.Ⅱ) Gene Mutation in Patients with Myelodysplastic Syndromes;

骨髓增生异常综合征与线粒体细胞色素氧化酶基因突变

Study on STK15 Gene Overexpression and p53 Gene Mutation in Centrosomal Abnormality of Laryngeal Carcinoma;

喉癌p53基因突变和STK15基因过表达与中心体异常相关性研究

A nonsense mutation of ADAR gene in a sporadic patient with dyschromatosis symmetrica hereditaria

1例遗传性对称性色素异常症患者ADAR基因突变研究