Linhart M S, Chu K, Evans U N, Dunkel V C, Arnold J
J Environ Pathol Toxicol. 1980 Aug;4(1):1-21.
The In Vitro information System (IVIS) provides for the collection, maintenance, analysis and reporting of mutagenesis data for the In Vitro Carcinogenesis Program of the Carcinogenesis Testing Program in the National Cancer Institute. Initial development or IVIS focused on the microbial mutagenicity assays conducted in a collaborative study in four laboratories. Information is collected about contract management, chemicals, microorganisms strain checks, preparation of activation enzymes, test results, and confirmation of mutation. IVIS provides for editing and maintenance of the information on computers at the National Institutes of Health. Analysis and reporting features were designed to assist both laboratory investigators and NCI staff in evaluating the mutagenic activity of test compounds. The analysis has focused on two principal goals: using the computer to examine the results of each test to determine if the test was adequate for a further statistical analysis; and secondly, if the plate counts are adequate, developing statistics that indicate whether there is a positive or negative trend. Reports have been developed for tabular displays of test results, frequency distributions, dose response graphs and statistical computations.
体外信息系统(IVIS)用于收集、维护、分析和报告美国国立癌症研究所致癌测试项目中体外致癌计划的诱变数据。IVIS的初步开发聚焦于在四个实验室开展的一项合作研究中进行的微生物致突变性试验。收集的信息包括合同管理、化学品、微生物菌株检查、活化酶制备、测试结果以及突变确认。IVIS可在美国国立卫生研究院的计算机上对信息进行编辑和维护。分析和报告功能旨在协助实验室研究人员和美国国立癌症研究所工作人员评估受试化合物的诱变活性。分析主要集中在两个主要目标上:利用计算机检查每项测试的结果,以确定该测试是否足以进行进一步的统计分析;其次,如果平板计数足够,制定统计数据以表明是否存在阳性或阴性趋势。已经开发了用于以表格形式显示测试结果、频率分布、剂量反应图和统计计算的报告。