工作流引擎在继电保护管理系统中的应用

继电保护管理系统中关键业务的应用开发离不开工作流技术的支持。针对于此,通过对系统的实际开发需求的分析,在传统的关系数据库的基础上,提出了一个适用于关键业务开发的基于关系数据库的轻量级工作流引擎的框架结构。深入讨论了采用关系数据库来设计工作流引擎的原因,并详细地给出了相关的设计原理以及具体的表示和实现方法。其原型已经应用到实际的继电保护管理系统中。实践证明,利用此工作流引擎可以显著地缩短业务的开发周期。     

Enhanced susceptibility of a highly resistant strain of houseflies to ingestion of potassium bromide

Résumé Une souche de mouches résistant au dichlorodiphényl-trichloroéthane fut trouvée plus susceptible à l'ingestion de bromure de potassium qu'une souche de mouches normales. Il s'agit là évidemment d'une caractéristique spécifique de cette souche, étant donné que l'on n'a pas pu observer une suceptibilité plus élevée vis-à-vis du bromure de potassium chez des souches résistant à d'autres insecticides.     

Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease

Linkage disequilibrium (LD) mapping provides a powerful method for fine-structure localization of rare disease genes, but has not yet been widely applied to common disease. We sought to design a systematic approach for LD mapping and apply it to the localization of a gene (IBD5) conferring susceptibility to Crohn disease. The key issues are: (i) to detect a significant LD signal (ii) to rigorously bound the critical region and (iii) to identify the causal genetic variant within this region. We previously mapped the IBD5 locus to a large region spanning 18 cM of chromosome 5q31 (P<10(-4)). Using dense genetic maps of microsatellite markers and single-nucleotide polymorphisms (SNPs) across the entire region, we found strong evidence of LD. We bound the region to a common haplotype spanning 250 kb that shows strong association with the disease (P< 2 x 10(-7)) and contains the cytokine gene cluster. This finding provides overwhelming evidence that a specific common haplotype of the cytokine region in 5q31 confers susceptibility to Crohn disease. However, genetic evidence alone is not sufficient to identify the causal mutation within this region, as strong LD across the region results in multiple SNPs having equivalent genetic evidence-each consistent with the expected properties of the IBD5 locus. These results have important implications for Crohn disease in particular and LD mapping in general.     

A genome-wide association study of metabolic traits in human urine

We present a genome-wide association study of metabolic traits in human urine, designed to investigate the detoxification capacity of the human body. Using NMR spectroscopy, we tested for associations between 59 metabolites in urine from 862 male participants in the population-based SHIP study. We replicated the results using 1,039 additional samples of the same study, including a 5-year follow-up, and 992 samples from the independent KORA study. We report five loci with joint P values of association from 3.2 × 10(-19) to 2.1 × 10(-182). Variants at three of these loci have previously been linked with important clinical outcomes: SLC7A9 is a risk locus for chronic kidney disease, NAT2 for coronary artery disease and genotype-dependent response to drug toxicity, and SLC6A20 for iminoglycinuria. Moreover, we identify rs37369 in AGXT2 as the genetic basis of hyper-β-aminoisobutyric aciduria.     

Monophyletic origin of Lake Victoria cichlid fishes suggested by mitochondrial DNA sequences

Lake Victoria, together with its satellite lakes, harbours roughly 200 endemic forms of cichlid fishes that are classified as 'haplochromines' and yet the lake system is less than a million years old. This 'flock' has attracted attention because of the possibility that it evolved within the lake from one ancestral species and that biologists are thus presented with a case of explosive evolution. Within the past decade, however, morphology has increasingly emphasized the view that the flock may be polyphyletic. We sequenced up to 803 base pairs of mitochondrial DNA from 14 representative Victorian species and 23 additional African species. The flock seems to be monophyletic, and is more akin to that from Lake Malawi than to species from Lake Tanganyika; in addition, it contains less genetic variation than does the human species, and there is virtually no sharing of mitochondrial DNA types among species. These results confirm that the founding event was recent.     

Enhancing Organisational Innovation Capability Through Systemic Action Research: A Case of a Swiss SME in the Food Industry

This paper presents detailed insights into the nature of innovation dynamics of an SME operating in the food industry. Furthermore, the paper highlights how Action Research has changed and enhanced SME??s capability to innovate. Within the exploratory action research based case study described in this article, the researchers interacted closely with one company with regards to a newly launched innovation process over a time period of more than 18 months. The analysis contributes to the fields of action research and innovation research in three respects: First, it exemplifies how systemic action research as a method can be applied on the organisational level in the private sector. Second, it demonstrates how useful action research can be for fostering the innovativeness and creativity of a company. Lastly, the analysis illustrates the extensive time horizon of an action research project.