Leclair Benoît, Frégeau Chantal J, Bowen Kathy L, Fourney Ron M
National DNA Data Bank, Royal Canadian Mounted Police, 1200 Vanier Parkway, Ottawa, Ontario, Canada K1G 3M8.
Electrophoresis. 2004 Mar;25(6):790-6. doi: 10.1002/elps.200305718.
Base-calling precision of short tandem repeat (STR) allelic bands on dynamic slab-gel electrophoresis systems was evaluated. Data was collected from over 6000 population database allele peaks generated from 468 population database samples amplified with the AmpF/STR Profiler Plus (PP) kit and electrophoresed on ABD 377 DNA sequencers. Precision was measured by way of standard deviations and was shown to be essentially the same, whether using fixed or floating bin genotyping. However, the allelic ladders have proven more sensitive to electrophoretic variations than database samples, which have caused some floating bins of D18S51 to shift on occasion. This observation prompted the investigation of polyacrylamide gel formulations in order to stabilize allelic ladder migration. The results demonstrate that, although alleles comprised in allelic ladders and questioned samples run on the same gel should migrate in an identical manner, this premise needs to be verified for any given electrophoresis platform and gel formulation. We show that the compilation of base-calling data is a very informative and useful tool for assessing the performance stability of dynamic gel electrophoresis systems, stability on which depends genotyping result quality.
评估了动态平板凝胶电泳系统上短串联重复序列(STR)等位基因条带的碱基识别精度。数据收集自使用AmpF/STR Profiler Plus(PP)试剂盒扩增并在ABD 377 DNA测序仪上进行电泳的468个群体数据库样本所产生的6000多个群体数据库等位基因峰。通过标准差来衡量精度,结果表明,无论是使用固定分型还是浮动分型,精度基本相同。然而,已证明等位基因阶梯比对数据库样本的电泳变化更敏感,这有时会导致D18S51的一些浮动分型发生偏移。这一观察结果促使人们对聚丙烯酰胺凝胶配方进行研究,以稳定等位基因阶梯的迁移。结果表明,尽管在同一凝胶上运行的等位基因阶梯和可疑样本中的等位基因应以相同方式迁移,但对于任何给定的电泳平台和凝胶配方,这一前提都需要进行验证。我们表明,碱基识别数据的汇编是评估动态凝胶电泳系统性能稳定性的一个非常有信息价值和有用的工具,而基因分型结果的质量取决于该稳定性。