In vitro information system for collection and analysis of experimental data.

M S Linhart, K Chu, U N Evans, V C Dunkel, J Arnold
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Abstract

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.

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体外信息系统用于实验数据的收集和分析。
体外信息系统(IVIS)为国家癌症研究所的癌变检测项目的体外癌变项目提供了诱变数据的收集、维护、分析和报告。IVIS的最初开发重点是在四个实验室的合作研究中进行的微生物诱变性分析。收集有关合同管理、化学品、微生物菌株检查、激活酶的制备、测试结果和突变确认的信息。IVIS负责编辑和维护国立卫生研究院计算机上的信息。分析和报告功能旨在帮助实验室研究人员和NCI工作人员评估测试化合物的致突变活性。分析集中在两个主要目标上:使用计算机检查每次测试的结果,以确定测试是否足以进行进一步的统计分析;其次,如果板块数量足够,发展统计表明是否有积极或消极的趋势。已经开发了测试结果、频率分布、剂量反应图和统计计算的表格显示报告。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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