Graham Eleanor A M
Forensic Pathology Unit University of Leicester, Leicester Royal Infirmary, Robert Kilpatrick Building, LE2 7LX, Leicester, United Kingdom,
Forensic Sci Med Pathol. 2005 Mar;1(1):65-7. doi: 10.1385/FSMP:1:1:065.
The use of the short-tandem repeat (STR) as the DNA marker of choice in forensic profiling has lead to the construction of criminal intelligence databases that now contain millions of profiles used in the detection and linking of suspects and scenes. The incredible size and success rate of current systems have ensured that efforts to move away from STR profiling and toward the use of alternate DNA markers are practically impossible, mainly because of the financial implications involved in such a move. Problems are routinely encountered when template DNA is of suboptimal condition, as is commonly the case in the forensic laboratory, whereby full profile generation of degraded samples is not possible. A redesigned amplification protocol that results in the generation of shorter polymerase chain reaction products yet is fully compatible with current STR databases has been introduced: the MiniPlex.
短串联重复序列(STR)作为法医鉴定中首选的DNA标记,已促使建立了犯罪情报数据库,这些数据库目前包含数百万个用于侦查嫌疑人及关联案发现场的DNA图谱。当前系统规模惊人且成功率高,这使得放弃STR图谱分析而转向使用其他DNA标记的努力几乎不可能实现,主要是因为这一转变涉及巨大的资金投入。当模板DNA条件欠佳时(法医实验室中常见这种情况),通常会遇到问题,即无法从降解样本中生成完整的图谱。一种重新设计的扩增方案被引入,该方案能产生更短的聚合酶链反应产物,但仍与当前的STR数据库完全兼容:MiniPlex。