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用于短串联重复序列等位基因高速分型的ALF DNA测序仪评估。

Evaluation of the ALF DNA sequencer for high-speed sizing of short tandem repeat alleles.

作者信息

Decorte R, Cassiman J J

机构信息

Center for Human Genetics, University of Leuven, Belgium.

出版信息

Electrophoresis. 1996 Oct;17(10):1542-9. doi: 10.1002/elps.1150171007.

Abstract

DNA typing of short tandem repeat (STR) loci with automated real-time analysis of the fluorescent polymerase chain reaction (PCR) products has given forensic DNA analysis a new dimension. In the present work, the ALF DNA sequencer was evaluated for automated size determination of tetra-nucleotide STRs at high speed. Short gel plates, with a well-to-laser distance of 10 cm, allowed for the analysis of four STR loci (HUMvWF, HUMTH01, D21S11 and HPRT) in one gel lane in less than 75 min. Allele size determination was done with two external allelic ladders for each locus. Lane-to-lane variations were overcome by the inclusion in each lane of two fluorescent PCR products of constant size (123 and 375 bp) that migrated below and above the multiplex of the four STR loci. The accuracy of sizing and allele detection within and between different gels was high (99.89%) for all four STR systems investigated and the gels could be reloaded without a decrease in accuracy of the allele size estimation. This way, the throughput of the system was increased, which is of interest for linkage studies, gene mapping, and population diversity studies.

摘要

通过对荧光聚合酶链反应(PCR)产物进行自动化实时分析来对短串联重复序列(STR)位点进行DNA分型,为法医DNA分析带来了新的维度。在本研究中,对ALF DNA测序仪进行了评估,以实现四核苷酸STR的高速自动化大小测定。短凝胶板的孔到激光距离为10厘米,可在不到75分钟的时间内对一个凝胶泳道中的四个STR位点(HUMvWF、HUMTH01、D21S11和HPRT)进行分析。每个位点使用两个外部等位基因梯来确定等位基因大小。通过在每个泳道中加入两个大小恒定(123和375 bp)的荧光PCR产物来克服泳道间的差异,这两个产物在四个STR位点的多重产物之下和之上迁移。对于所研究的所有四个STR系统,不同凝胶内部和之间的大小测定和等位基因检测准确性都很高(99.89%),并且凝胶可以重新加载而不会降低等位基因大小估计的准确性。通过这种方式,该系统的通量得以提高,这对于连锁研究、基因图谱绘制和群体多样性研究具有重要意义。

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