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After a power spectrum is constructed, empirical wavelet coefficients are used to detect the jump points in the function to obtain the strong consistent estimator of the position and number of the frequencies. Numerical simulations show this method is reliable.

根据它们的协方差函数可以表示为一个Fourier级数,而其Fourier系数可通过协方差函数的逆变换得到的特性,我们对于零均值的近周期相关序列构造了类似于周期图的函数,并构造其经验小波系数,利用频率处于此函数的尖点的特性,以及此性质在经验小波系数中的反映,来确定频率的个数和位置,所有的估计量都是强相合的,此外,数值模拟的结果表明,我们的方法是有效的。

However, because of the positive sequence of fundamental frequency, there are still some shortages for wavelet transform in the use of harmonic measurement of three-phase dissymmetrical system. A new approach of harmonic measurement based on Period-interleaving of MALLAT arithmetic for dissymmetrical system is put forward. Analysis and experiment based on TMS320LF2407 Digital Signal Processor are made. And the result of experiment reveals that the proposed method based on Period-interleaving is valid in the use of harmonic measurement of three-phase dissymmetrical system.

但是,目前小波变换在三相不对称系统的谐波检测中存在着无法分离基波正序信号的不足,本文就此提出了一种用于三相不对称系统的基于周期交错的小波MALLAT多分辨率分解的测量方法,详细介绍了该算法的原理、流程及计算公式,同时以TMS320LF2407数字信号处理器为核心建立了实验系统对该算法进行了实验,实验结果证明该周期交错-小波变换算法可以有效地检测出三相不对称系统中的有害电流。

The representation of sequences is very helpful for the research of their linear complexity,so this paper we first research trace representation of periodic sequences,and the trace representation of a New Generalized Cyclotomic Sequence of order two of length pq is given,then for 2~mp~n period binary sequences,where p is an odd prime and 2 is a primitive root modulo p~2,we present a relation-ship between the linear complexity and the minimum value k for which the k-error linear complexity is strictly less than the linear complexity and have the upper bound and lower bound of the value k, finally we discuss the k-error linear complexity of legendre sequences,also have the upper bound and lower bound of the value k,and discusses the situation where the linear complexity drop again for some Legendre sequences.

序列的表达形式对于其线性复杂度的研究是十分有帮助的,本文我们首先研究的是周期序列的迹表示,给出了2阶pq长度的扩展分圆序列的迹表示,然后讨论了周期为2~mp~n(m≥2)序列的线性复杂度与使得线性复杂度变小的最小的k值的关系,给出了k值的上界和下界,这里p为奇素数,2是模p~2的本原根,并通过例子讨论了其线性复杂度的稳定性,最后对Legendre序列k-错线性复杂度进行了分析,也给出了k值的上界和下界,并对某些Legendre序列讨论了线性复杂度再次下降的情况。

The equivalent definition of the minimal strong component is given, and it discusses the relation between the standard form and the minimal strong component in the paper. Consequently, the theory is proved that the periodicity of a fuzzy matrix is the least common multiple of periodicity of its minimal strong component.

给出了极小强支的等价定义,讨论了模糊矩阵的标准型与极小强支关系,从而得到了模糊矩阵周期是极小强支周期的最小公倍数的定理。

The spectrum analysis was applied to analyze the fluctu- ation of flocs diameter during the spring tide and the neap tide.

分析表明,长江口徐六泾处细颗粒泥沙絮凝体粒径存在着明显的变化周期:大潮表层存在7.86h,3.93h和2.95h的变化周期;小潮表层存在8.38h和3.14h的变化周期;大潮底层存在3.33h和1.19h的变化周期。

It is shown from the study results that (1) SSC has obvious neap-spring and seasonal variations with periods being 14.7 days and 368 days, respectively, on an average, SSC during the spring tide was 2.96 times as much as that during the neap tide, and SSC in winter was twice as much as that in summer;(2) correlation coefficient between daily SSC and tidal range on the same day in a mean neap-spring period of 15 days was 0.86, and correlation coefficients between tidal range and daily SSC with one day and two day lag were 0.99 and 0.93, respectively, which indicates that the effect of tidal range variation on SSC has a one day or two day hysteresis;(3) the monthly mean SSC was negatively correlated with the monthly mean water discharge at the Changjiang River Datong station, especially well with the water discharge with a lag of 19 days.

悬沙浓度具有显著的大、小潮和季节性变化,变化周期分别为14.7 d和368 d,平均而言,大潮为小潮的2.96倍,冬季为夏季的2倍;2)平均大、小潮半月周期中日悬沙浓度与同日潮差之间的相关系数为0.86,与前1日潮差之间的相关系数为0.99,与前2日潮差之间的相关系数为0.93,反映潮差变化对悬沙浓度的影响有1~2d的滞后效应;3)月均悬沙浓度与长江大通站的月均流量呈显著负相关,尤其与流量滞后19d的相关性最好。

The results showed that the quasi-period of floes diameter in the surface water during the spring tide included 7.86 h, 3.93h and 2.95h; those in the same water during the neap tide included 8.38h and 3.14h; those in the bottom water during the spring tide included 3.33h and 1.19h.

分析表明,长江口徐六泾处细颗粒泥沙絮凝体粒径存在着明显的变化周期:大潮表层存在7.86h, 3.93h和2.95h的变化周期;小潮表层存在8.38h和3.14h的变化周期;大潮底层存在3.33h和1.19h的变化周期。

The stable clones are further identified by RT-PCR and Western blot; 6 MTT assay is used to investigate the effect of ZNRD1 on the cell growth of cells (AGS, SGC7901, MKN28, NIH3T3, GES-1); 7 Soft agar assay is used to investigate the effect of ZNRD1 on the clonality of cells (AGS, MKN28); 8 Nude mice assay is used to investigate the effect of ZNRD1 on the cell growth of gastric cancer cells (AGS, MKN28); 9 Flow cytometry is used to investigate the effect of ZNRD1 on the cell cycle distribution of cells (AGS, MKN28, NIH3T3, GES-1); 10 Flow cytometry is used to investigate the effect of ZNRD1 on the cell apoptosis of cells (AGS, MKN28, NIH3T3); 11 MTT assay is used to investigate the effect of ZNRD1 on the drug sensitivity of cancer cells (SGC7901, SGC7901/VCR, HL-60, HL-60/VCR) in vitro; 12 SRCA is used to investigate the effect of ZNRD1 on the drug sensitivity of gastric cancer cells (SGC7901, SGC7901/VCR) in vivo; 13 Flow cytometry is used to investigate the effect of ZNRD1 on adriamycin accumulation of cancer cells (SGC7901, SGC7901/VCR, HL-60, HL-60/VCR); 14 Transmission electron microscope is used to investigate the effect of ZNRD1 on the sensitivity of SGC7901 cells towards drug-induced apoptosis; 15 Flow cytometry and DNA ladder assay are used to investigate the effect of ZNRD1 on the sensitivity of cells (SGC7901, SGC7901/VCR, HL-60/VCR) towards drug-induced apoptosis; 16 Microarray is used to investigate the profiling of ZNRD1-responsive genes in gastric cancer cells (AGS, MKN28, SGC7901, SGC7901/VCR); 17 RT-PCR and Western blot are used to identify the results of microarray; 18 Reporter gene assay is used to investigate the effect of ZNRD1 on the transcriptional activity of cyclin D1; 19 Reporter gene assay is used to investigate the effect of ZNRD1 on the transcriptional activity of MDR1; 20 Kinase assay is used to investigate the effect of ZNRD1 on the activity of cyclin E-CDK2 kinase; 21 The antisensenucleic acids of p21 is used to inhibit the expression of p21, and flow cytometry is used to investigate the effect of p21 on ZNRD1-induced cell cycle arrest in gastric cancer cells; 22 The antisensenucleic acids of p27 is used to inhibit the expression of p27, and flow cytometry is used to investigate the effect of p27 on ZNRD1-induced cell cycle arrest in gastric cancer cells; 23 Liposome is used to up-regulate the expression of Skp2, and flow cytometry is used to investigate the effect of Skp2 on ZNRD1-induced cell cycle arrest in gastric cancer cells; 24 Western blot is used to investigate the effect of ZNRD1 on the stability of Skp2 and p27 in gastric cancer cells; 25 MVD assay is used to investigate the effect of ZNRD1 on the angiopoietic activity of gastric cancer cells; 26 ELISA is used to investigate the effect of ZNRD1 on the expression of VEGF165 in gastric cancer cells; 27 The roles of DARPP-32 in MDR of gastric cancer cells are investigated using gene transfection, MTT assay, SRCA, flow cytometry and DNA ladder assay.

应用杂交瘤技术制备ZNRD1的首个单克隆抗体;2)利用RT-PCR、Western blot和免疫组化检测ZNRD1在胃癌组织、胃炎组织、正常胃上皮组织、胃癌细胞和正常胃组织上皮细胞中的表达;3)构建ZNRD1的小干扰RNA载体,并测序鉴定;4)利用脂质体将ZNRD1的真核表达载体及其空载体转染胃癌细胞(AGS、SGC7901、MKN28)和小鼠成纤维细胞(NIH3T3),G418筛选后进行鉴定;5)利用脂质体将ZNRD1的小干扰RNA载体及其空载体转染药敏胃癌细胞(SGC7901)、正常胃组织上皮细胞(GES-1)、对长春新碱耐药的胃癌细胞(SGC7901/VCR)、药敏白血病细胞(HL-60)、对长春新碱耐药的白血病细胞(HL-60/VCR),G418筛选后进行鉴定;6)利用MTT实验检测ZNRD1高/低表达对细胞(AGS、SGC7901、MKN28、NIH3T3、GES-1)生长的影响;7)通过软琼脂克隆形成实验检测上调ZNRD1对AGS、MKN28细胞克隆形成能力的影响;8)通过裸鼠成瘤实验检测上调ZNRD1对AGS、MKN28细胞体内成瘤性的影响;9)通过流式细胞仪分析ZNRD1高/低表达对细胞(AGS、MKN28、NIH3T3、GES-1)的细胞周期的影响;10)通过流式细胞仪分析上调ZNRD1对细胞(AGS、MKN28、NIH3T3)的凋亡的影响;11)通过MTT实验检测ZNRD1高/低表达对细胞(SGC7901、SGC7901/VCR、HL-60、HL-60/VCR)体外药物敏感性的影响;12)通过肾包膜下移植法检测ZNRD1高/低表达对细胞(SGC7901、SGC7901/VCR)体内药物敏感性的影响;13)通过流式细胞仪分析ZNRD1高/低表达对细胞(SGC7901、SGC7901/VCR、HL-60、HL-60/VCR)内阿霉素蓄积和泵出的影响;14)通过透射电镜检测上调ZNRD1对SGC7901细胞凋亡敏感性的影响;15)通过流式细胞仪和DNA梯度试验检测ZNRD1高/低表达对细胞(SGC7901、SGC7901/VCR、HL-60)凋亡敏感性的影响;16)通过基因芯片检测ZNRD1高/低表达对胃癌细胞内基因表达谱的影响;17)利用RT-PCR、Western blot对基因芯片的结果进行鉴定;18)利用报告基因实验检测ZNRD1对cyclin D1的启动子活性的调节作用;19)利用报告基因实验检测ZNRD1高/低表达对MDR1的启动子活性的调节作用;20)利用激酶试验检测ZNRD1对cyclin E-CDK2 激酶活力的影响;21)利用反义核酸技术抑制p21的表达;通过流式细胞仪检测抑制p21对ZNRD1介导的细胞周期阻滞的影响;22)利用反义核酸技术抑制p27的表达;通过流式细胞仪检测抑制p27对ZNRD1介导的细胞周期阻滞的影响;23)利用脂质体转染法上调Skp2的表达;通过流式细胞仪检测上调Skp2对ZNRD1介导的细胞周期阻滞的影响;24)利用Western blot检测ZNRD1对p27和Skp2的蛋白稳定性的影响;25)利用微血管密度实验检测ZNRD1对AGS、MKN28细胞裸鼠移植瘤微血管形成的影响;26)利用ELISA检测ZNRD1对AGS、MKN28细胞培养上清和移植瘤匀浆中VEGF165含量的影响;27)利用脂质体转染法、MTT实验、肾包膜下移植法、流式细胞仪和DNA梯度试验检测新耐药相关分子DARPP-32对细胞(SGC7901、SGC7901/VCR、对阿霉素耐药的胃癌细胞SGC7901/ADR)多药耐药表型的影响;利用脂质体转染法和MTT实验检测下调ZNRD1对DARPP-32介导的胃癌多药耐药的调控作用。

A high-speed digital-to-analog converter measurement method acquires and quantizes an analog ramp output by the DAC corresponding to a digital ramp input to produce a quantized ramp, determines a start and end of the quantized ramp, obtains a difference between the quantized ramp and an ideal ramp to produce a quantized periodic signal, determines a frequency for a qualified peak from an FFT of the quantized periodic signal, produces a mask filtered periodic signal from an iFFT around the qualified peak, and determines a sample window spanning a local maximum and minimum for each period of the quantized periodic signal.

一种高速模拟数字转换器测量方法,采集和量化由DAC输出的相应于数字斜坡输入的模拟斜坡以产生量化的斜坡,确定量化的斜坡的开始和结束,获得量化的斜坡和理想的斜坡之间的差值以产生量化的周期信号,从量化的周期信号的FFT中确定合格峰值的频率,从合格峰值周围的iFFT中产生屏蔽过滤的周期信号,并且在量化的周期信号的每一周期内确定跨越局部最大值和最小值的采样窗口。

We also observed that the genomic regions with higher GC content tend to form nucleosome with greater stability.

我们在线虫核小体DNA中观察到的175-nt周期信号与在阴道滴虫基因序列中观察到的120.9-nt周期信号为同一类信号,反应的都是缠绕在核小体上的DNA与位于核小体之间的DNA在核苷酸组成上的不同。

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