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Main_grating
超结构光纤光栅基本特性，利用matlab进行仿真模拟，计算反射谱和投射普(Super-structure fiber grating basic characteristics
)
- 2012-04-14 15:08:47下载
- 积分：1
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BL-Lac-object
类星体光变分析，在matlab环境下W-M函数模拟光变，内含大量BL Lac原始观测数据！(light curve of BL Lac object)
- 2013-01-15 09:23:32下载
- 积分：1
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cv_fenxi1
matlab 代码，主要用于计算一数据矩阵的标准差，方差，变异系数，话三维曲面图(matlab code, data matrix used to calculate a standard deviation, variance, coefficient of variation, then D surface chart)
- 2013-10-31 19:58:00下载
- 积分：1
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QPSK_TX
Quadrature phase shift keying transmitter matlab m file.
- 2009-10-01 01:49:51下载
- 积分：1
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my
说明： VBLAST 2发2收情况下的链路,可以实现误码率的计算
(STBC)
- 2010-04-21 14:16:43下载
- 积分：1
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MATLAB6.0--handbook
MATLAB6.0数学手册 pdf格式电子书 一共包含7章节(MATLAB6.0 handbook)
- 2011-12-12 10:35:27下载
- 积分：1
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UFVM
with this code it could drwa evrythings about modal parametrs of structures and otherthings
- 2015-02-11 19:28:33下载
- 积分：1
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LLTSA降维
说明： 这个是KPCA核主成分分析的代码，好用，里面也带有范例(This is the KPCA kernel principal component analysis code, which is easy to use and also contains examples.)
- 2019-12-01 20:24:24下载
- 积分：1
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bode_graph
matlab 仿真的一个系统的波的图，简单易学好用(matlab simulation of a system of wave maps, easy to learn easy to use)
- 2011-07-07 20:04:48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
