Roche Hungary Ltd, Budaörs, Hungary.
Pathol Oncol Res. 2010 Sep;16(3):421-6. doi: 10.1007/s12253-010-9274-6. Epub 2010 May 19.
In the diagnostic workflow we need to think in algorithms, containing more assays. One of the most important task in the management of cancer patient is to detect nucleic acid sequence changes in clinical specimens. Before using the most expensive method to analyze direct our targets, a screening assay is needed to reduce the number of samples. In the detection of gene-sequence alterations classical screening methods are available, as SSCP, DGGE or TGGE, (Finke Exp Clin Endocrinol Diabetes 104:92-97, 1996; Lessa and Applebaum Mol Ecol 2:119-129, 1993) however these are very time consuming processes. At this time in the molecular lab the real-time PCR equipments are very popular and with the function of melting curve analysis it can be a very convenient, simple and cost-efficient screening method.
在诊断工作流程中,我们需要思考包含更多检测的算法。在癌症患者的管理中,最重要的任务之一是检测临床标本中的核酸序列变化。在使用最昂贵的方法分析直接目标之前,需要进行筛选检测以减少样本数量。在基因序列改变的检测中,有几种经典的筛选方法,如 SSCP、DGGE 或 TGGE(Finke Exp Clin Endocrinol Diabetes 104:92-97, 1996; Lessa and Applebaum Mol Ecol 2:119-129, 1993),然而这些方法非常耗时。此时,在分子实验室中,实时 PCR 设备非常流行,并且具有熔解曲线分析功能,因此它可以成为一种非常方便、简单且具有成本效益的筛选方法。