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一种用于同时定量人类总DNA和男性DNA的实时PCR检测方法的发育验证。

Developmental validation of a real-time PCR assay for the simultaneous quantification of total human and male DNA.

作者信息

Krenke Benjamin E, Nassif Nadine, Sprecher Cynthia J, Knox Curtis, Schwandt Melissa, Storts Douglas R

机构信息

Promega Corporation, 2800 Woods Hollow Road, Madison, WI 53711, USA.

出版信息

Forensic Sci Int Genet. 2008 Dec;3(1):14-21. doi: 10.1016/j.fsigen.2008.07.004. Epub 2008 Sep 9.

Abstract

Multiplex human short tandem repeat analysis demands reliable DNA quantification to consistently produce interpretable genotypes. The Plexor HY System is a multiplex quantitative PCR assay to quantify total human and male DNA. We performed developmental validation of the Plexor HY System to demonstrate the performance capabilities and limitations of the assay for forensic applications. Validation studies examined: (a) human specificity, (b) sensitivity, (c) quantification of degraded DNA, (d) impact of inhibitors, (e) male/female mixture and Y-assay male specificity, (f) reproducibility and concordance and (g) population studies.

摘要

多重人类短串联重复序列分析需要可靠的DNA定量,以始终如一地产生可解释的基因型。Plexor HY系统是一种多重定量PCR检测方法,用于定量总人类DNA和男性DNA。我们对Plexor HY系统进行了开发验证,以证明该检测方法在法医应用中的性能能力和局限性。验证研究包括:(a)人类特异性,(b)灵敏度,(c)降解DNA的定量,(d)抑制剂的影响,(e)男性/女性混合样本和Y检测的男性特异性,(f)重复性和一致性,以及(g)群体研究。

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