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MLPAnalyzer: Data Analysis Tool for Reliable Automated Normalization of MLPA Fragment Data

机译:MLPAnalyzer:用于可靠自动归一化MLPA片段数据的数据分析工具

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Background: Multiplex Ligation dependent Probe Amplification (MLPA) is a rapid, simple, reliable and customized method for detection of copy number changes of individual genes at a high resolution and allows for high throughput analysis. This technique is typically applied for studying specific genes in large sample series. The large amount of data, dissimilarities in PCR efficiency among the different probe amplification products, and sample-to-sample variation pose a challenge to data analysis and interpretation. We therefore set out to develop an MLPA data analysis strategy and tool that is simple to use, while still taking into account the above-mentioned sources of variation.Materials and Methods: MLPAnalyzer was developed in Visual Basic for Applications, and can accept a large number of file formats directly from capillary sequence systems. Sizes of all MLPA probe signals are determined and filtered, quality control steps are performed, and variation in peak intensity related to size is corrected for. DNA copy number ratios of test samples are computed, displayed in a table view and a set of comprehensive figures is generated. To validate this approach, MLPA reactions were performed using a dedicated MLPA mix on 6 different colorectal cancer cell lines. The generated data were normalized using our program and results were compared to previously performed array-CGH results using both statistical methods and visual examination.Results and Discussion: Visual examination of bar graphs and direct ratios for both techniques showed very similar results, while the average Pearson moment correlation over all MLPA probes was found to be 0.42. Our results thus show that automated MLPA data processing following our suggested strategy may be of significant use, especially when handling large MLPA data sets, when samples are of different quality, or interpretation of MLPA electropherograms is too complex. It remains, however, important to recognize that automated MLPA data processing may only be successful when a dedicated experimental setup is also considered.
机译:背景:多重连接依赖性探针扩增(MLPA)是一种快速,简单,可靠和定制的方法,可以高分辨率检测单个基因的拷贝数变化,并可以进行高通量分析。该技术通常用于研究大样本系列中的特定基因。大量数据,不同探针扩增产物之间PCR效率的差异以及样品之间的差异给数据分析和解释带来了挑战。因此,我们着手开发一种易于使用的MLPA数据分析策略和工具,同时仍考虑到上述变化的来源。材料和方法:MLPAnalyzer是在Visual Basic for Applications中开发的,可以接受大量直接来自毛细管序列系统的文件格式数。确定并过滤所有MLPA探针信号的大小,执行质量控制步骤,并校正与大小有关的峰强度变化。计算测试样品的DNA复制数比率,并以表格视图显示,并生成一组综合数字。为了验证该方法,使用专用的MLPA混合物对6种不同的结直肠癌细胞系进行了MLPA反应。使用我们的程序对生成的数据进行归一化,并使用统计方法和视觉检查将结果与先前执行的阵列CGH结果进行比较。结果与讨论:两种技术的条形图和直接比率的视觉检查显示的结果非常相似,而发现所有MLPA探针的皮尔逊矩相关性均为0.42。因此,我们的结果表明,遵循我们建议的策略进行自动MLPA数据处理可能会发挥重要作用,尤其是在处理大型MLPA数据集,样本质量不同或MLPA电泳图的解释过于复杂时。但是,重要的是要认识到,只有在还考虑了专用实验设置的情况下,自动化MLPA数据处理才可能成功。

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