In defense acquisition system, testing and evaluation is a very important procedure that can ensure the completeness of capability while deciding whether to mass-produce or purchase weapons systems. But it always includes realistic restrictions that involve a variety of stakeholders, but lack of time, resources, and budget. Therefore, in the process of planning a test and evaluation, proper number of prototypes and reliability of test results, along with test items and evaluation criteria, are frequently discussed as sensitive agendas. In reality, however, rather than statistical judgments, the number of prototypes and tests are determined by business logic such as duration and budget. Otherwise, most theoretical studies do not adequately reflect the business logic of test assessment. In this study, we propose a number of prototype and tests method that can statistically reasonably verify the performance of the inorganic system considering the characteristics of each test and evaluation project. To this end, we consider the theory related to determining the number of prototypes and tests, and present examples by separating whether to secure the magnitude of effects that have a significant impact on statistical judgment. This study could contribute to the development of empirical methodologies that can adequately coordinate reality and theory in the field of defense test evaluation while ensuring statistical reliability of test evaluation results.

Most traditional genome sequencing projects involving infectious viruses include culturing and purification of the virus. This can present difficulties as an analysis of multiple populations from multiple locations may be required to acquire sufficient amount of high-quality DNA for sequence analysis. The electrophoretic method provides a strategy whereby the genomic DNA sequences of the Korean isolate of Pieris rapae granulovirus (PiraGV-K) were analyzed by purifying it from host DNA by pulsed-field gel electrophoresis, thus simplifying sampling and labor time. The genomic DNA of infected P. rapae was embedded in agarose plugs, digested with a restriction nuclease and methylase, and pulsed-field gel electrophoresis (PFGE) was used to separate PiraGV-K DNA from the DNA of P. rapae, followed by mapping of fosmid clones of the separated viral DNA. The double-stranded circular genome of PiraGV-K encodes 120 open reading frames (ORFs), covering 92% of the sequenced genome. BLAST and ORF arrangement showed the presence of 78 homologs to other genes in the database. The mean overall amino acid identity of PiraGV-K ORFs was highest with the Chinese isolate of PiraGV (~99%), followed up with Choristoneura occidentalis ORFs at 58%. PiraGV-K ORFs were grouped, according to function, into 10 genes involved in transcription, 11 involved in replication, 25 structural protein genes, and 15 auxiliary genes. Genes for Chitinase (ORF 10) and cathepsin (ORF11), involved in the liquefaction of the host, were found in the genome. The recovery of PiraGV-K DNA genome by pulse-field electrophoretic separation from host genomic DNA had several advantages, compared with its isolation from particles harvested as virions or inclusions from the P. rapae host. We have sequenced and analyzed the 108,658 bp PiraGV-K genome purified by the pulsed field electrophoretic method. The method appears to be applicable to the analysis of genomes of large viruses. The chitinase, identified by PiraGV-K genome sequence, was functionally characterized by quantitative PCR, Western blot analysis, immunohistochemistry and transmission electron microscopy.