登录
首页 » Java » 38388___introduction_to_simulink_with_engineering

38388___introduction_to_simulink_with_engineering

于 2013-12-02 发布 文件大小:3991KB
0 273
下载积分: 1 下载次数: 3

代码说明:

  Introduction to Simulink with Engineering Applications.

下载说明:请别用迅雷下载,失败请重下,重下不扣分!

发表评论

0 个回复

  • my-work-project
    to find pitch record and play signal
    2011-04-20 06:24:46下载
    积分:1
  • MATLAB
    signal proccessing and furier transform
    2014-10-24 00:52:36下载
    积分:1
  • WhiteandcoloredNoise_series
    利用白噪声序列和传递函数生成有色噪声的源代码,很实用(Using white noise sequence and colored noise transfer function to generate source code, very useful)
    2014-01-15 11:13:16下载
    积分:1
  • qpsk_BER
    实现随机信号序列的QPSK调制和相干解调,观察信号的星座图,计算误比特率和误码率。(this code is designed for the signal s QPSK modulation and demodulation exactly. Meanwhile, the BER and SER were estimated and drawed.)
    2014-03-13 16:58:27下载
    积分:1
  • scankernel
    Kernel for All Windows Version make all of them going to die hardware
    2014-10-02 16:19:05下载
    积分:1
  • memoria
    LTE model in simulink, to stady the effect of channel
    2011-12-17 07:40:39下载
    积分:1
  • CMI-DHB3-CMI
    在matlab中对AMI、HDB3、CMI等码进行编码,(In matlab encode for AMI)
    2013-12-13 23:32:24下载
    积分:1
  • RoutingCN_PferentialProb
    complex network routing based on the preferential probability as the scale-free features
    2009-11-09 19:16:26下载
    积分:1
  • 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
  • WriteFile
    Simple code to write a file in C
    2015-04-03 20:09:23下载
    积分:1
  • 696516资源总数
  • 106914会员总数
  • 0今日下载