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多重连接依赖探针扩增产物的自动分析(以用于产前非整倍体检测的商业试剂盒为例)。

Automatic analysis of multiplex ligation-dependent probe amplification products (exemplified by a commercial kit for prenatal aneuploidy detection).

作者信息

Gerdes Tommy, Kirchhoff Maria, Bryndorf Thue

机构信息

Department of Clinical Genetics, Rigshospitalet, Copenhagen, Denmark.

出版信息

Electrophoresis. 2005 Nov;26(22):4327-32. doi: 10.1002/elps.200500390.

DOI:10.1002/elps.200500390
PMID:16240299
Abstract

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.

摘要

为用于常规产前诊断,我们基于一种商业多重连接依赖探针扩增(MLPA)试剂盒开发了自动非整倍体检测的软件和方法。软件和方法确保了可靠、客观且快速的工作流程,并且可应用于其他类型的MLPA试剂盒。在MLPA扩增产物获得CE认证后,该软件会自动识别每个探针的峰面积,将其相对于测试样品的相邻峰面积进行归一化,计算相对于由正常样品创建的参考值的比率,并针对归一化程序的副作用对该比率进行补偿,该副作用会根据存在的非整倍体类型将所有染色体正常的DNA峰面积轻微上调或下调。对于染色体13、18、21、X和Y,计算探针可靠性加权平均比率值及相应的标准差,并测试比率值偏离1.0左右参考区间的显著性。p≤1%提示非整倍体,1<p≤5%提示可能存在非整倍体。归一化面积距离相应参考值超过4个标准差的单个峰提示可能存在部分缺失或增加。自动评估样品质量。无需对照探针。使用该软件和方法两年后,我们得出结论,获得了可靠、客观且快速的工作流程。

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Electrophoresis. 2005 Nov;26(22):4327-32. doi: 10.1002/elps.200500390.
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