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NSGA-II
说明: 通用NSGA2程序,里面有详细的注释,亲测可用(General NSGA2 program, which has detailed notes, pro test available)
- 2021-01-29 16:27:14下载
- 积分:1
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CAPON
现代谱估计的CAPON等算法仿真,对谱估计的研究者有用(Modern Spectral Estimation Algorithm Simulation CAPON)
- 2010-12-19 11:10:42下载
- 积分:1
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SJohnsonLDPCintro
有个ldpc码的介绍,很全面,很好,适合于初学者(A introduction abuat LDPC codes , very comprehensive, very good, and suitable for beginners)
- 2014-12-08 21:07:13下载
- 积分:1
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Matlab-SimPowerSystems
Matlab-PSB-Electrical Sources使用说明(Matlab-PSB-Electrical Sources)
- 2013-05-04 20:08:31下载
- 积分:1
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wlp
matlab编写的声卡采集声音信号并可以播放出来的gui界面。(matlab write sound card and can play sound signals collected from the gui interface.)
- 2011-04-30 16:42:26下载
- 积分:1
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54
说明: 《高阶谱分析》例题5.4,根据零极点分布建立传递函数,求解冲击响应和系统输出,求解高阶矩或累计量,计算倒谱参数。( Higher-order spectral analysis, Example 5.4, according to the distribution of zeros and poles of transfer function to establish, to solve the impact of response and system output, for solving high-order moment or cumulant calculated cepstrum parameters.)
- 2008-01-16 15:51:50下载
- 积分:1
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Guass_Newton
高斯牛顿函数的最优化算法matlab源程序。。。(Function by the Gauss-Newton optimization algorithm matlab source code)
- 2013-02-25 14:36:14下载
- 积分:1
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Particle-swarm-algorithm-source
基本粒子群算法源程序,开发环境是MATLAB,吐血推荐,易改实用!(Particle swarm algorithm source)
- 2013-02-26 16:41:34下载
- 积分:1
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Dpajialai
基于MATLAB的确定性系统的分岔与混沌的设计程序(MATLAB-based deterministic system, bifurcation and chaos in the design process)
- 2009-12-30 21:44:09下载
- 积分:1
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pcreff
一个强大的工具分析 寻找 逆转录(逆转录)跟随由聚合酶链反应,该程序定量分析信使核糖核酸。定量表达基因水平,特别是能为低级的丰富信使核糖核酸提供分析工具。(Reverse transcription(RT) followed by PCR is a powerful tool for the detection and quantification of mRNA. It is the most sensitive method for the detection and quantification of gene expression levels, in particular for low abundance mRNA.
The relative quantification is based on the expression ratio of a target gene versus a reference gene. Some mathematical models have already been developed to calculate the relative expression ratios, with or without efficiency correction. Normally the PCR efficiency is set at 2 (the max possible value) for the reference and target gene, but a difference in PCR efficiency of 0.03 between the target and reference gene, the falsely calculated difference in expression ratio is 46 in case of Et<Er and 209 in the case of Et>Er. The difference will increase dramatically by higher efficiency differences: i.e. DE=0.05 (27 and 338 ) and DE=0.1 (7.2 and 1083 )
This function computes the efficiency of PCR reaction and is based on my function MYREGR)
- 2011-01-22 00:52:34下载
- 积分:1