利用软件故障注入提高软件测试覆盖率

软件测试过程是软件生命周期中提高软件质量的重要阶段，但无论结构测试还是接收测试（AT），都很难测试程序的所有分枝，对于容错软件的异常处理和故障恢复代码的测试尤其困难。使得这些代码中可能包含软件故障，反而成为软件质量的隐患，为此采用程序变异的方法对被测软件进行故障注入，用强制的方法执行被测分支，从而提高软件的测试覆盖率。     

图像增强的自适应免疫算法

介绍了自适应免疫算法的基本原理及实现步骤，并将其应用到图像的增强处理中，在传统的图像管理处理中，针对图像灰度分布的不同情况，需要定义相应的灰度变换函数。Tubbs将图像增强处理中几种常用的非线性变换函数表示成一个归一化的非完全Beta函数，但确定Beta函数参数仍是一个复杂的问题，本文利用自适应免疫算法来确定该变换函数的最佳参数值，通过对自然图像的仿真实验可以看出本文方法的有效性。     

L-谷氨酸氧化酶高产菌株的快速筛选及诱变育种

用谷氨酸氧化酶测试液浸湿白卷纸置于菌落上,根据白卷纸上显示红色快慢、深浅,就能大致测得该菌落菌株产酶能力高低。该法可靠性大、工作量小、操作简便,显示结果快。利用该法,配合亚硝酸诱变,在短暂三个月内,将L-谷氨酸氧化酶产生菌株产酶能力提高了约25倍。     

γ射线对大蒜的诱变效应

用γ射线处理三个大蒜品种的鳞茎,VM_1代出苗率及植株存活率降低,生长发育受阻,抽苔率降低,鳞茎变小,并出现形态学畸变,VM_1代主要表现为辐射损伤,不宜进行突变性状选择;VM_2代仍有较严重的辐射损伤,开始出现纯合突变,性状变异范围扩大、变异度增大,抽苔期及质量性状选择可在VM_2进行,但不宜进行株高突变及高产变异类型的选择;VM_3代开始出现鳞茎数量性状有益突变,可以进行高产突变类型选择。     

转座子的起源及其和物种进化的关系

关于转座子的属性及其起源问题现在还没有解决,在这篇论文中,作者经过分析提出了转座子由病毒或逆转录病毒退化而来的观点,并且阐述了转座子与物种进化之间的关系,主要从转座子影响物种适应性和引起基因突变,染色体畸变两个方面进行了说明。     

Molecular genetic basis for the rhino mouse from Chinese KM subcolony

Both the rhino mouse and hairless mouse resulted from hairless gene mutation, but they show different phenotypes of skin physiology. The rhino mouse has more similar histological characters to human papular alopecia.Therefore rhino mouse is a good experimental animal model for human papular alopecia. This study reports a hairless mouse named rhino KIZ, arose from KM colony in Kunming Institue of Zoology, by systematic studies on morphology,skin histopathology, gene sequence, pedigree and protein domain analysis. The results demonstrate that a C-to-T transition in exon 11 of hr gene (The mutant gene has been applied for a Chinese patent (patent No. 03135280)) results in the rhino KIZ. The rhino KIZ with clear genetic mechanism will be a useful animal model.     

The molecular mechanisms of congenital hypofibrinogenaemia

Congenital hypofibrinogenaemia is characterized by abnormally low levels of fibrinogen and is usually caused by heterozygous mutations in the fibrinogen chain genes (, and ). However, it does not usually result in a clinically significant condition unless inherited in a homozygous or compound heterozygous state, where it results in a severe bleeding disorder, afibrinogenaemia. Various protein and expression studies have improved our understanding of how mutations causing hypo- and afibrinogenaemia affect secretion of the mature fibrinogen molecule from the hepatocyte. Some mutations can perturb chain assembly as in the 153 Cys Arg case, while others such as the B Leu Arg and the B414 Gly Ser mutations allow intracellular hexamer assembly but inhibit protein secretion. An interesting group of mutations, such as 284 Gly Arg and 375 Arg Trp, not only cause hypofibrinogenaemia but are also associated with liver disease. The nonexpression of these variant chains in plasma fibrinogen is due to retention in the endoplasmic reticulum, which in turn leads to hypofibrinogenaemia.Received 17 December 2003; received after revision 19 January 2004; accepted 21 January 2004     

Human mitochondrial tRNAs in health and disease

The human mitochondrial genome encodes 13 proteins, all subunits of the respiratory chain complexes and thus involved in energy metabolism. These genes are translated by 22 transfer RNAs (tRNAs), also encoded by the mitochondrial genome, which form the minimal set required for reading all codons. Human mitochondrial tRNAs gained interest with the rapid discovery of correlations between point mutations in their genes and various neuromuscular and neurodegenerative disorders. In this review, emerging fundamental knowledge on the structure/function relationships of these particular tRNAs and an overview of the large variety of mechanisms within translation, affected by mutations, are summarized. Also, initial results on wide-ranging molecular consequences of mutations outside the frame of mitochondrial translation are highlighted. While knowledge of mitochondrial tRNAs in both health and disease increases, deciphering the intricate network of events leading different genotypes to the variety of phenotypes requires further investigation using adapted model systems.Received 3 December 2002; received after revision 14 January 2003; accepted 27 January 2003     

基于自适应混合变异进化策略的神经模糊系统及应用研究

针对现存神经模糊系统中存在的问题,提出了基于自适应混合变异进化策略的神经模糊系统采用改进的最近邻域聚类算法对输入空间进行模糊聚类,确定模糊规则数以及模糊规则前件,这样做精简了模糊规则,不会因输入变量的增加而造成"维数灾难”;采用自适应混合进化策略确定模糊规则的后件,明显提高了算法的收敛速度和精度.将本文提出的基于自适应进化策略的神经模糊系统用于某炼油厂航煤干点的软测量建模,结果表明,该系统具有结构简单、建模精度高、泛化能力强等优点.     

集成粒子群优化算法在电网规划中的应用

电网规划是一个大规模、复杂的、具有非线性离散变量和多约束的多目标数学优化问题。在优化过程中,考虑了投资费用、可靠性和对环境的影响等三个因素。提出将模拟退火优化方法嵌入粒子群优化算法中,以此构建集成粒子群优化算法。在搜索过程中还加入变异操作来增加种群多样性,以避免早熟收敛。局部搜索增加了算法的开发能力,而变异操作提高了算法的探测能力。探测与开发能力的平衡,通过两个阈值来实现。通过对一220kv电力传输系统的实例研究表明,集成粒子群优化算法局部搜索能力有显著提高。