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state vector相关的网络例句

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与 state vector 相关的网络例句 [注:此内容来源于网络,仅供参考]

In order to deal with attributes reduction, one of the major problems in rough set theory, an attributes reduction algorithm was proposed based on scan vector, and a new conception of discernible vector was defined by which the information table can be transformed into discernible vector sets.

针对粗糙集理论中属性约简问题,提出了一种基于扫描向量的属性约简方法。

This paper proposes a general method based on Principal Component Analysis to analyze network anomalies. The method divides the traffic matrix into normal subspace and anomalous subspace, maps the traffic vector into normal subspace, gets the distance from detected vector to average normal vector, and detects anomalies based on that distance.

文章提出一种分析网络异常的通用方法,该方法运用主成分分析手段将高维空间划分为对应正常和异常网络行为的子空间,并将流量向量影射在正常子空间中,使用基于距离的度量来检测宏观网络流量异常事件。

The method divides the traffic matrix into normal subspace and anomalous subspace, maps the traffic vector into normal subspace, gets the distance from detected vector to average normal vector, and detects anomalies based on that distance.

文章提出一种分析网络异常的通用方法,该方法运用主成分分析手段将高维空间划分为对应正常和异常网络行为的子空间,并将流量向量影射在正常子空间中,使用基于距离的度量来检测宏观网络流量异常事件。

The CryCI gene and essential regulation elements cut from the plasmid pGF4ABC were inserted into yeast expression vector pPIC9K and plant expression vector pBI 121.1, so we got the secretive yeast expression plasmid pPIC9KBC and plant high-efficiency expression plasmid pGBIF4ABC, Fifty-two His+Muts transformants were obtained after the expression vector pPIC9KBC was introduced into Pichia pasoris, KM7I strain, by electroporation.

将pGF4ABC上的融合杀虫基因CryCI分别克隆到酵母表达载体pPIC9K和植物表达载体pBI121.1上,构建成融合杀虫基因的分泌型酵母表达载体pPIC9KBC和高效植物表达载体pGBIF4ABC。

It points out that under the hard-switching PWM pattern, the movement speed of flux linkage is adjusted by zero space voltage vector, but when soft-switching PWM pattern is used, effect time of space voltage vector vary greatly, sometimes even no zero space voltage vector exist.

指出在硬开关PWM模式下,磁链的运动速度靠零空间电压矢量调节;而在软开关PWM模式下,空间电压矢量的作用时间发生了很大变化,有时甚至没有零空间电压矢量。

A new SVM method suitable for four-switch inverter fed PMSM DTC system was proposed. By analyzing the property of the equivalent zero space vector and its imitation scheme in detail, the paper introduced a zero-vector partition idea, which is usually adopted in the SVPWM modulation, to the composition of desired space vector.

该文针对四开关逆变器供电PMSM DTC系统的特殊性,采用了一种新型SVM方法,分析了等效零矢量模拟技术,将传统SVPWM调制中的劈零思想引入到空间矢量的合成上。

Experimental results show that the zero effort miss vector calculated by using approximate formulas is close to the real miss vector. Under the conditions of small initial errors, the satisfied results can be obtained by approximate function. The zero effort miss vector obtained can be used for the preliminary design and analysis of kinetic interceptor guidance.

测试结果表明该近似算法得到的零控脱靶量与真实值比较接近,在较小初始偏差条件下,简化的近似计算公式能给出满意的结果,所得零控脱靶量可用于空间动能拦截制导系统的初步设计与分析。

Methods:The total RNA was extracted from mouse RAW264.7 cells stimulated by LPS.The sequence including the whole length of HMGB1 was amplified by RT-PCR and inserted into pMD-19T.The combinant vector was used as a template for PCR which was cloned into vector pMD-19T,then subcloned into expression vector pET-26b with pelB signal sequence and His-Taq sequence.After transforming E.coli BL21(DE3) and four hours induction by IPTG,HMGB1 expression confirmed by SDS-PAGE and the purification was performed by Ni2+-chelate affinity chromatograph.

脂多糖刺激后的RAW264.7细胞,提取总RNA,经RT-PCR扩增出含HMGB1的目的片段,克隆于pMD-19T载体,再亚克隆至含有pelB引导肽及His-标签肽的高效表达载体pET-26b,转化大肠杆菌BL21(DE3),经IPTG诱导后行SDS-PAGE鉴定目标蛋白表达,用镍鳌合琼脂糖凝胶亲和层析法分离纯化含His-标签肽的目的蛋白。

Methods:The total RNA was extracted from mouse RAW264.7 cells stimulated by LPS.The sequence including the whole length of HMGB1 was amplified by RT-PCR and inserted into pMD-19T.The combinant vector was used as a template for PCR which was cloned into vector pMD-19T,then subcloned into expression vector pET-26b with pelB signal sequence and His-Taq sequence.

脂多糖刺激后的RAW264.7细胞,提取总RNA,经RT-PCR扩增出含HMGB1的目的片段,克隆于pMD-19T载体,再亚克隆至含有pelB引导肽及His-标签肽的高效表达载体pET-26b,转化大肠杆菌BL21(DE3),经IPTG诱导后行SDS-PAGE鉴定目标蛋白表达,用镍鳌合琼脂糖凝胶亲和层析法分离纯化含His-标签肽的目的蛋白。

The combinant vector was used as a template for PCR which was cloned into vector pMD-19T,then subcloned into expression vector pET-26b with pelB signal sequence and His-Taq sequence.After transforming E.coli BL21(DE3) and four hours induction by IPTG,HMGB1 expression confirmed by SDS-PAGE and the purification was performed by Ni2 -chelate affinity chromatograph.

脂多糖刺激后的RAW264.7细胞,提取总RNA,经RT-PCR扩增出含HMGB1的目的片段,克隆于pMD-19T载体,再亚克隆至含有pelB引导肽及His-标签肽的高效表达载体pET-26b,转化大肠杆菌BL21(DE3),经IPTG诱导后行SDS-PAGE鉴定目标蛋白表达,用镍鳌合琼脂糖凝胶亲和层析法分离纯化含His-标签肽的目的蛋白。

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