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Journal ArticleDOI

Developmental validation of the Quantifiler(®) HP and Trio Kits for human DNA quantification in forensic samples.

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TLDR
The Quantifiler HP and Trio Kits' improved performance provides better predictive ability for results with downstream, newest-generation STR assays, and their shortened time-to-result allows more efficient integration into the forensic casework analysis workflow.
Abstract
The quantification of human genomic DNA is a necessary first step in the DNA casework sample analysis workflow. DNA quantification determines optimal sample input amounts for subsequent STR (short tandem repeat) genotyping procedures, as well as being a useful screening tool to identify samples most likely to provide probative genotypic evidence. To better mesh with the capabilities of newest-generation STR analysis assays, the Quantifiler(®) HP and Quantifiler(®) Trio DNA Quantification Kits were designed for greater detection sensitivity and more robust performance with samples that contain PCR inhibitors or degraded DNA. The new DNA quantification kits use multiplex TaqMan(®) assay-based fluorescent probe technology to simultaneously quantify up to three human genomic targets, allowing samples to be assessed for total human DNA, male contributor (i.e., Y-chromosome) DNA, as well as a determination of DNA degradation state. The Quantifiler HP and Trio Kits use multiple-copy loci to allow for significantly improved sensitivity compared to earlier-generation kits that employ single-copy target loci. The kits' improved performance provides better predictive ability for results with downstream, newest-generation STR assays, and their shortened time-to-result allows more efficient integration into the forensic casework analysis workflow.

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Citations
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Journal ArticleDOI

Isolation and genetic analysis of pure cells from forensic biological mixtures: The precision of a digital approach

TL;DR: This study reports here the development of an application-specific DEPArray™ workflow enabling the detection and recovery of pure homogeneous cell pools from simulated blood/saliva and semen/Saliva mixtures, providing full genetic match with genetic profiles of corresponding donors.
Journal ArticleDOI

Evaluation of four commercial quantitative real-time PCR kits with inhibited and degraded samples

TL;DR: The results of this study indicate that all kits were comparable in accurately predicting quantities of high quality DNA down to the sub-picogram level, however, the InnoQuant(R) HY kit showed the highest precision across the DNA concentration range tested in this study.
Journal ArticleDOI

Prediction of autosomal STR typing success in ancient and Second World War bone samples

TL;DR: The PowerQuant kit is capable of identifying bone DNA samples that will not yield useful STR profiles using the NGM kit, and it can be used as a predictor of autosomal STR typing success of bone extracts obtained from ancient and WWII skeletal remains.
Journal ArticleDOI

In-field collection and preservation of decomposing human tissues to facilitate rapid purification and STR typing.

TL;DR: The results indicate that modified TENT preservative and FTA® Elute Cards both preserved DNA from relatively fresh tissue for up to six months at room temperature, however, mostly partial profiles were produced from decomposed tissues when stored for up-to- six months compared to when tissues were processed immediately following collection.
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Successful nuclear DNA profiling of rootless hair shafts: a novel approach

TL;DR: The utilization of an enhanced DNA extraction methodology for hairs, in combination with a recently developed novel, nuclear DNA typing assay, InnoTyper® 21, to improve the success rate for obtaining informative results from highly compromised, degraded, and trace forensic samples such as rootless hair shafts is reported.
References
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Journal ArticleDOI

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TL;DR: These Alu element-based alternative methods for the rapid identification and quantitation of human DNA, inter-Alu PCR and intra-ALU PCR have several advantages over currently available systems, including the high copy number of subfamily-specific Alu repeats in the human genome.
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