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Optimization of Computer Software Settings Improves Accuracy of Pulsed-Field Gel Electrophoresis Macrorestriction Fragment Pattern Analysis

机译:计算机软件设置的优化提高了脉冲场凝胶电泳宏观限制性片段图谱分析的准确性

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摘要

Computer-assisted analysis of pulsed-field gel electrophoresis (PFGE) libraries can facilitate comparisons of fragment patterns present on multiple gels. We evaluated the ability of the Advanced Analysis (version 4.01) and Database (version 1.12) modules of the Phoretix gel analysis software package (Nonlinear USA, Inc., Durham, N.C.) to accurately match DNA fragment patterns. Two gels containing 38 lanes of SmaI-digested Enterococcus faecalis OG1RF DNA were analyzed to assess the impact of (i) varying the lane position of the standards, (ii) using gel plugs made at different times, and (iii) normalizing the fragment patterns by using molecular weight (MW) algorithms versus retardation factor (Rf) algorithms. Two sets of PFGE libraries (one containing SmaI restriction patterns from 62 Enterococcus faecium isolates and the other containing SmaI restriction patterns of 89 Staphylococcus aureus isolates) were analyzed to assess the impact of varying the matching tolerance algorithm (designated as the vector box setting [VBS]) in the Phoretix software. Varying the lane position of standards on a gel and using gel plugs made on different days resulted in different VBSs, although it was not possible to judge whether those differences were statistically significant. Normalization of E. faecalis OG1RF fragment patterns by Rf and MW methodology yielded no statistically significant differences in variability between the same fragment on different lanes. Suboptimal VBSs decreased the specificity with which related isolates were grouped together in dendrograms. The optimal VBS for analysis of PFGE fragment patterns from E. faecalis isolates differed from that for S. aureus isolates and sometimes was not that recommended by the manufacturer. Thus, computer-assisted analysis of PFGE patterns seemed to compensate for the intra- and intergel variation evaluated in the present study, and optimizing the software for the species to be tested was a critical preliminary step before further PFGE library analysis.
机译:脉冲场凝胶电泳(PFGE)库的计算机辅助分析可以促进对多种凝胶上存在的片段模式进行比较。我们评估了Phoretix凝胶分析软件包(Nonlinear USA,Inc.,Durham,N.C.)的Advanced Analysis(4.01版)和Database(1.12版)模块准确匹配DNA片段模式的能力。分析了含有38条泳道的SmaI消化的粪肠球菌OG1RF DNA的两种凝胶,以评估(i)改变标准泳道位置,(ii)使用在不同时间制作的胶塞和(iii)标准化片段模式的影响通过使用分子量(MW)算法与延迟因子(Rf)算法进行比较。分析了两组PFGE库(一组包含来自62种粪肠球菌的SmaI限制模式,另一组包含89种金黄色葡萄球菌的SmaI限制模式),以评估改变匹配耐受算法(称为向量框设置[VBS]的影响])在Phoretix软件中。改变标准品在凝胶上的泳道位置,并使用在不同日期制作的凝胶塞会产生不同的VBS,尽管无法判断这些差异是否具有统计学意义。通过Rf和MW方法对粪肠球菌OG1RF片段模式进行归一化,在不同泳道上的同一片段之间的变异性没有统计学上的显着差异。次优的VBS降低了将相关分离物以树状图分组的特异性。用于分析粪肠球菌分离株的PFGE片段模式的最佳VBS与金黄色葡萄球菌分离株的VBS不同,有时制造商也不建议这样做。因此,计算机辅助分析PFGE模式似乎补偿了本研究中评估的凝胶内和凝胶间变异,优化待测物种的软件是进一步进行PFGE库分析之前的关键的初步步骤。

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