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首页> 外文期刊>Electrophoresis: The Official Journal of the International Electrophoresis Society >Automatic analysis of multiplex ligation-dependent probe amplification products (exemplified by a commercial kit for prenatal aneuploidy detection).
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Automatic analysis of multiplex ligation-dependent probe amplification products (exemplified by a commercial kit for prenatal aneuploidy detection).

机译:自动分析多重连接依赖性探针扩增产物(以用于产前非整倍性检测的商业试剂盒为例)。

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摘要

For use in routine prenatal diagnostics, we developed software and methods for automatic aneuploidy detection based on a commercial multiplex ligation-dependent probe amplification (MLPA) kit. Software and methods ensure a reliable, objective, and fast workflow, and may be applied to other types of MLPA kits. Following CE of MLPA amplification products, the software automatically identified the peak area for each probe, normalized it in relation to the neighboring peak areas of the test sample, computed the ratio relative to a reference created from normal samples, and compensated the ratio for a side effect of the normalization procedure that scaled all chromosomally normal DNA peak areas slightly up or down depending on the kind of aneuploidy present. For the chromosomes 13, 18, 21, X, and Y, probe reliability weighted mean ratio values and corresponding SDs were calculated, and the significance for being outside a reference interval around ratio 1.0 was tested. p < or = 1% suggested aneuploidy and 1 < p < or = 5% suggested potential aneuploidy. Individual peaks, where the normalized area was situated more than 4 SD from the corresponding reference, suggested possible partial deletion or gain. Sample quality was automatically assessed. Control probes were not required. Having used the software and methods for two years, we conclude that a reliable, objective, and fast workflow is obtained.
机译:为了在常规产前诊断中使用,我们开发了基于商业多重连接依赖探针扩增(MLPA)试剂盒的自动非整倍性检测软件和方法。软件和方法可确保可靠,客观和快速的工作流程,并可应用于其他类型的MLPA套件。按照MLPA扩增产物的CE标准,软件会自动识别每个探针的峰面积,相对于测试样品的相邻峰面积进行归一化,计算相对于正常样品创建的参考的比例,并补偿根据存在的非整倍性的类型,将所有染色体正常DNA峰面积略微缩放的归一化程序的副作用。对于染色体13、18、21,X和Y,计算了探针可靠性加权平均比率值和相应的SD,并测试了在比率1.0附近的参考区间之外的显着性。 p <或= 1%表示非整倍性,1 <或= 5%表示潜在非整倍性。各个峰(归一化面积位于距相应参考值大于4 SD处)表明可能存在部分缺失或增益。自动评估样品质量。不需要对照探针。使用了两年的软件和方法,我们得出的结论是,获得了可靠,客观和快速的工作流程。

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