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PAPER2

于 2015-02-24 发布 文件大小:409KB
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  The PAPR Problem in OFDM Transmission New Directions for a Long-Lasting Problem

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    频率域建模,根据类型分为面向模拟滤波器的s域内建模和面向数字滤波器的z域内建模。 (Frequency domain modeling, according to the type of analog filters into the s-oriented domain modeling and digital filter z-oriented domain modeling.)
    2009-02-08 11:22:04下载
    积分:1
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    This function is for optimization when you draw contour
    2014-09-18 02:50:10下载
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    SAR回波成像仿真程序,采用非线性调频尺度变标算法,并可通过修改参数设置运动误差(SAR echo imaging simulation program, the use of non-linear scaling algorithm FM scale, and set the motion error by modifying the parameters)
    2016-05-19 16:21:51下载
    积分:1
  • 16QAM
    简单的数字传输系统---主要是对16-QAM数字基带传输系统进行仿真,基带调制和解调的输出信号都是复数信号。(Simple digital transmission system--- mainly simulate the 16-QAM digital baseband transmission system, the output signals of the baseband modulation and demodulation are complex signals.)
    2009-03-09 17:04:25下载
    积分:1
  • m_sequence
    说明:  使用Matlab软件来产生PN序列的程序(Using Matlab software program to generate PN sequences)
    2010-04-04 16:16:41下载
    积分:1
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    2012-04-27 18:15:59下载
    积分:1
  • offset_matrix_generation
    移动通信mimo信道建模中用到的小程序3。(Used in mobile communication mimo channel modeling program.)
    2012-11-05 21:16:08下载
    积分:1
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    a pre-processing box for standard Microarrays data set
    2010-03-02 03:13:17下载
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    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
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