Bang bang control of unified chaotic system

The unified chaotic system contains the Lorenz system and the Chen system as two dual systems at the two extremes of its parameter spectrum. This paper presents the design of bang bang controller for unified system and multitude of numerical experiments under various control parameters. Numerical experiments meet the theoretic proof perfectly and convincingly demonstrated the controller can be effectively used for unified systems with uncertainty of the equilibrium points. The method enriches the applications of chaotic control. Foundation item: Supported by the National Natural Science Foundation of China(50209012) Biography: Deng Xiao-ming (1980-), male, Master candidate, research direction: chaos control.     

基于神经网络的企业信用等级评估

企业信用等级评估是金融领域重要的问题，论文采用人工神经网络模型研究企业信用等级的评估问题，按照企业样本在信用等级的分布状况来抽样，然后，根据企业样本性质的不同，将其分为制造业和非制造业两大类，利用偏相关分析方法建立了企业信用评级的指标体系，此外，还介绍了几种企业信用评级常用的评估模型，并将神经网络评估模型的性能和其他的信用评估模型作了比较，实验结果表明神经网络模型具有更好的预测准确性。     

管理系统的最经济控制问题

依据最经济控制问题的概念及其对无确定性数学模型系统分析存在的局限性，对现代管理系统最经济控制问题，提出了在满足系统基本要求前提下。实现控制功能及品质与控制成本比最佳或最划算的模型定义，并对管理系统的可靠性、ABC管理法、WSR方法论等方面的可靠性成本、运行成本和最佳收益等最经济控制问题进行了研究．     

Estimation and testing of time-varying coefficient regression models in the presence of linear restrictions

A linear regression model with random walk coefficients is extended to allow for linear restrictions between the coefficients to be satisfied at each point in time. Estimation in this model is shown to be no more involved than estimation in the standard model. It is also demonstrated how, after a slight modification to the testing problem, classical test procedures may be applied to the problem of testing for such restrictions. The performance of the Lagrange Multiplier test for a variety of different restrictions is then investigated via simulation. An empirical application involving testing for homogeneity in a random walk coefficient version of the AIDS model is given.     

DNA fingerprinting transforms the art of cell authentication.

The increasing diversity of new cell cultures is seriously stretching the capabilities of traditional methods of identification. DNA fingerprinting is set to play an important role in increasing confidence in the authenticity of cultures in research and industry.     

Periodic paralysis in quarter horses: a sodium channel mutation disseminated by selective breeding.

We recently reported on a linkage study within a Quarter Horse lineage segregating hyperkalaemic periodic paralysis (HYPP), an autosomal dominant condition showing potassium-induced attacks of skeletal muscle paralysis. HYPP co-segregated with the equine adult skeletal muscle sodium channel alpha subunit gene, the same gene that causes human HYPP. We now describe the Phe to Leu mutation in transmembrane domain IVS3 which courses the horse disease. This represents the first application of molecular genetics to an important horse disease, and the data will provide an opportunity for control or eradication of this condition.     

Prediction of the structure of a receptor-protein complex using a binary docking method.

To validate procedures of rational drug design, it is important to develop computational methods that predict binding sites between a protein and a ligand molecule. Many small molecules have been tested using such programs, but examination of protein-protein and peptide-protein interactions has been sparse. We were able to test such applications once the structures of both the maltose-binding protein (MBP) and the ligand-binding domain of the aspartate receptor, which binds MBP, became available. Here we predict the binding site of MBP to its receptor using a 'binary docking' technique in which two MBP octapeptide sequences containing mutations that eliminate maltose chemotaxis are independently docked to the receptor. The peptides in the docked solutions superimpose on their original positions in the structure of MBP and allow the formation of an MBP-receptor complex. The consistency of the computational and biological results supports this approach for predicting protein-protein and peptide-protein interactions.