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Exam
time windows usage example
- 2011-02-04 03:02:19下载
- 积分:1
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matlab-study
说明: 各种matlab的资料,很好的学习资料,供大家学习与交流使用,欢迎一起分享。(some kinds of study books,let s study and communication with each other. welcome to share with me.)
- 2011-02-21 10:33:05下载
- 积分:1
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三转角插值
说明: 三弯矩插值法
lagrange多项式插值
多项式最小二乘法
龙贝格积分法
分段线性插值
三转角插值
这些是数值分析中常用的集中经典方法,运用matlab展示出来!(three polynomial interpolation Hangzhou least squares polynomial interpolation Romberg integration subparagraph Line sex angle interpolation three interpolation these numerical analysis is commonly used in concentrated classical methods, and use Matlab show!)
- 2006-01-13 18:31:09下载
- 积分:1
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u5
说明: 这个MUSIC算法好像有点问题,望大家帮忙(the MUSIC algorithm appears to be a problem, we hope to see help)
- 2007-05-18 19:22:55下载
- 积分:1
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AP_proj
MATLAB PROGRAM TO DETERMINE CAPACITANCE OF PARALLEL PLATE CAPACITOR
- 2015-01-02 21:48:59下载
- 积分:1
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SCEGET
shuffled complex evolution method (function)
- 2013-12-13 03:54:02下载
- 积分:1
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FFT-Matlab
MATLAB下FFT变换实用2个例子,可以进行绘制fft波形及计算THD(The MATLAB FFT transform practical two examples can draw the fft waveforms and calculate THD)
- 2012-12-23 21:51:33下载
- 积分:1
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checkgeometry
有限元单元划分
checkgeometry(Finite Element unit division
checkgeometry)
- 2014-09-17 09:22:24下载
- 积分:1
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fir
matlab中实现有限相应滤波器FIR的程序(matlab limited to achieve the corresponding procedures for FIR Filter)
- 2008-01-03 14:30:29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