CLPSO

matlab常用函数查询，编程很有用的东西。(matlab commonly used functions query)

瞬时盲源分离代码，带有数据，可以直接运行，适合初学者！(Instant Blind Source Separation Code, with data that can be run directly for beginners!)

关于turbo码译码的仿真程序，简单实用，很受编码学者的青睐(The simulation on the turbo decoding process, simple and practical, popular with scholars of all ages code)

MatLab工程数学应用 非常有用的书 尤其是在数学应用方面(MatLab Application Engineering Mathematics book very useful especially in applications of mathematics)

设计一CQMFB，低通滤波器H_0 (z)来自一半带滤波器。该半带滤波器的长度为47，通带截止频率ω_p=0.42π，试给出H_0 (z)，H_1 (z)，G_0 (z)，G_1 (z)的幅频响应，单位抽样响应并画图。试着产生一信号，它由两个正弦加白噪声组成，一个在低频，一个在高频，正弦的频率及和白噪声的信噪比自己给定。试用所设计的滤波器组对该信号进行分解和重建。比较重建后的效果，并对结果继续进行分析。(Design a CQMFB, low pass filter H_0 (z) the half-band filter. The length of the half-band filter 47, passband cutoff frequency ω_p = 0.42π, try to give H_0 (z), H_1 (z), G_0 (z), G_1 (z) of the amplitude-frequency response, the unit sample response and Paint. Try to generate a signal that consists of two sinusoidal composition plus white noise, a low frequency, a high frequency in the signal to noise ratio, frequency and sine and white noise of its own given. Trial designed filter group that signal decomposition and reconstruction. Results were rebuilt, and the results continue to be analyzed.)

无迹卡尔曼滤波算法,用无迹卡尔曼滤波算法实现了跟踪中的误差估计(the function of ukf)

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)

This algorithm is ADI algorithm.

说明：  Matlab编程手册，一些编程的问题基本都能在这解决。(Matlab programming manual, some basic programming issues to resolve in this can.)

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