Akbari Akbar, Marthinsen Gunnhild, Lifjeld Jan T, Albregtsen Fritz, Wennerberg Liv, Stenseth Nils C, Jakobsen Kjetill S
Department of Informatics, University of Oslo, Oslo, Norway.
Electrophoresis. 2008 Mar;29(6):1273-85. doi: 10.1002/elps.200700523.
In CE the charged DNA strands are fractionated according to fragment lengths as they migrate through the capillary, since shorter DNA fragments pass through the sieving matrix faster. Multiplexed internal size standards are used to estimate the size of unknown DNA fragments. In the literature there are statements about migration abnormalities for the 250 and 340 bp fragments in the GeneScan-500 (GS500) internal size standards. Such anomalous migration of size standards could obviously introduce errors in the estimation of unknown fragments. Therefore, a number of analysis programs simply exclude some of these fragments. In the present work we first evaluate the effect of excluding each of the fragments in the internal size standards used in CE. Next, a method which is based on estimating the true values of the anomalous fragments is presented. The results obtained by the new method indicate a significant improvement compared to results obtained when one (or both) of the anomalous fragments in GS500 is (are) excluded or included when estimating the size of unknown DNA fragments. In the higher-molecular-weight region, the average error is reduced from 1.91 bp in ABI GeneMapper (excluding 250 bp) to 0.15 bp in the new method (using the estimated values for 250 and 340 bp). In the lower-molecular-weight region, excluding both fragments will improve the results by an average of 0.74 bp compared to ABI GeneMapper.
在毛细管电泳(CE)中,带电的DNA链在通过毛细管迁移时会根据片段长度进行分离,因为较短的DNA片段通过筛分基质的速度更快。多重内标用于估计未知DNA片段的大小。文献中有关于GeneScan-500(GS500)内标中250和340 bp片段迁移异常的报道。这种大小标准的异常迁移显然会在未知片段的估计中引入误差。因此,许多分析程序简单地排除了其中一些片段。在本研究中,我们首先评估了在CE中使用的内标中排除每个片段的影响。接下来,提出了一种基于估计异常片段真实值的方法。与在估计未知DNA片段大小时排除或包含GS500中的一个(或两个)异常片段时获得的结果相比,新方法获得的结果有显著改善。在较高分子量区域,平均误差从ABI GeneMapper中的1.91 bp(排除250 bp)降低到新方法中的0.15 bp(使用250和340 bp的估计值)。在较低分子量区域,与ABI GeneMapper相比,同时排除这两个片段将使结果平均提高0.74 bp。