New DNA Quantification Kits Enable Precision-Guided Forensic Analysis of Highly Compromised Human Samples

21 Feb 2014
Sarah Thomas
Associate Editor

Product news

Forensic scientists can now more quickly assess the quantity and quality of human DNA in highly compromised and degraded casework samples and provide the critical information needed to drive informed decisions on subsequent steps in the analysis process, thanks to two new Life Technologies quantification solutions announced today by Thermo Fisher Scientific.

At the same time, the company is also introducing a next generation sequencing (NGS)-based single nucleotide polymorphism (SNP) solution for laboratories interested in extending their interrogation capabilities on compromised DNA samples beyond the industry’s validated capillary electrophoresis (CE) platform. All three products -- Quantifiler Trio and Quantifiler HP (Human Plus) Quantification kits, and the HID-Ion AmpliSeq Identity Panel -- are being launched at the American Academy of Forensic Sciences conference, which is being held Feb. 17-22 in Seattle.

Overcoming the challenges of highly degraded and inhibited casework samples

Highly degraded and inhibited casework samples pose particular challenges for forensic scientists. Choosing the most appropriate path toward the short tandem repeat (STR) PCR reaction is difficult when the sample amount and integrity is not known with absolute certainty. A wrong decision can lead to poor results for such difficult casework samples, along with wasted resources and lab time. Both the Quantifiler Trio and HP DNA Quantification kits help overcome these obstacles and the associated guesswork through enhanced autosomal targets that have been designed for maximum quantification and reproducibility along with new tools to assess sample degradation and inhibition.

Both chemistries enable forensic analysts to screen samples more efficiently and better discriminate between human and non-human DNA, while the Quantifiler Trio kit features an improved male target for increased quantitation reliability in excess amounts of female DNA, commonly seen in sexual assault samples.

When paired with the new HID Real-Time PCR Analysis v1.2 Software, the complementary solutions drive well-informed workflow decisions before proceeding to the STR reaction. Efficiency has also been increased since 6 percent more casework samples can now be processed at once, as well as a 33 percent reduction in the PCR cycle to drive faster time to results.

NGS Identity Panels Drive Deep Analysis of Challenging Samples


The HID-Ion AmpliSeq Identity Panel is one of the first publically available, high-throughput NGS solutions. It was developed in collaboration with leading forensic scientists and enables researchers to identify degraded samples in 1.5 days from as little as 1 ng of input DNA.
Run on the Ion PGM system, the HID-Ion AmpliSeq Identity Panel enables 50 or more samples to be multiplexed to drive down cost, while delivering sample specificity and low match probabilities comparable to a 13-core CODIS STR set. It is also available with integrated software tools to easily analyze and export results.

New possibilities for forensic information

“The biggest impact [of next-generation sequencing] is that we will be able to combine a large number of genetic markers of different types in a single run, including markers such as STRs and SNPs, potentially even RNA that cannot be multiplexed with any other current technology,” said Dr. Manfred Kayser, department of Forensic Molecular Biology, Erasmus University, Rotterdam, The Netherlands. “This will open up new possibilities as various types of forensically relevant information can be obtained from a single sample in a single analysis.”

The Ion PGM System combines semiconductor sequencing technology with natural biochemistry to directly translate chemical information into digital data. It is designed to democratize sequencing and make it accessible to virtually any laboratory or research facility. The system’s simplicity eliminates the need for expensive optics and reduces complex chemistries to measure natural DNA extension.

“Life Technologies is continually innovating to ensure it is delivering the most advanced forensic analysis products to help prevent and solve crimes,” said Nadia Altomare, vice president and general manager, Human Identification, for Thermo Fisher Scientific. “To that end, our latest quantification kits and NGS-based identity panels empower our customers to make highly informed workflow decisions, and expand their capabilities to interrogate relevant genetic markers to help investigate challenging cases.”

For more information on the Quantifiler Trio and Quantifiler Human Plus DNA Quantification kits, and the HID-Ion AmpliSeq Identity Panel, visit the Life Technologies booth (#104) at the American Academy of Forensic Sciences conference (Feb. 17-21) in Seattle, Wash.

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Capillary ElectrophoresisCapillary electrophoresis (CE) is used to separate molecules based on charge, size and hydrophobicity. Pressure, voltage or a vacuum is used to introduce the sample to fused silica capillaries. Fluorescence, UV/Vis, UV or diode array detectors are used to visualize components. Types of CE systems include capillary electrochromatography (CEC), capillary zone electrophoresis and capillary gel electrophoresis. Find the best capillary electrophoresis equipment in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.PCR and Thermal CyclingPolymerase chain reaction (PCR) kits and thermal cyclers are used for the in vitro amplification of DNA permitting subsequent analysis and experimental procedures. Explore a range of high-quality polymerase, primers and nucleotides or simplify your workflow with a PCR mastermix. Find reverse transcription PCR (RT-PCR) and cDNA synthesis kits for RNA products and libraries. Quantitatively measure the amplification of DNA with real-time PCR (qPCR) and droplet digital PCR (ddPCR) kits and systems, and discover automated PCR setup solutions to increase throughput. Alternative DNA amplification methods also include recombinase polymerase amplification (RPA) kits. Find the best PCR kits and thermal cyclers and purification equipment in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.SNPs TechnologySingle nucleotide polymorphisms (SNPs) are individual base variations in a DNA sequence. SNPs are used in research to study predispositions to disease and drug discovery. Products for studying single nucleotide polymorphisms include SNP arrays and detection systems to detect polymorphisms, SNP typing systems for genotyping DNA, and PCR to amplify specific SNPs.DNA / RNA Extraction and PurificationPurified DNA and RNA are required for numerous downstream molecular biology applications. Consequently, the importance of high-quality DNA/RNA extraction and purification equipment cannot be underestimated. Many purification kits are available and are typically optimized for nucleic acid type and source, including plasmid DNA, genomic DNA, mRNA, RNA and viral nucleic acid purification kits. Automated extraction and purification of nucleic acids can be implemented with magnetic bead separator instruments or high-throughput purification workstations. Find the best DNA/RNA extraction and purification equipment in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.DNA SequencingDNA sequencing, such as sanger sequencing, is a biological technique that determines the precise order of nucleotide bases in a fragment or template of DNA. DNA sequencers and genetic analyzers are based on capillary electrophoresis, where labeled DNA fragments are electrophoretically separated by size as they migrate through a polymer. Find the best DNA sequencing products, including DNA sequencing kits, genomic libraries and genetic identity kits in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.Next Generation SequencingNext-generation sequencing (NGS), also known as whole-genome sequencing, high-throughput sequencing and massive parallel sequencing, produces and analyses thousands to millions of nucleotide sequences at once. Sequencing systems operate via varying technologies depending on the manufacturer, including sequencing by synthesis, ligation, pyrosequencing, ion semiconductor and single-molecule real-time sequencing. For NGS, library preparation is paramount to successful sequencing. In this section, explore a range of library preparation kits, from targeted, amplicon-based or hybridization-based kits including epigenomic, transcriptomic and genomic workflows to fragmentation kits. Find the best next-generation sequencing products in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.
New DNA Quantification Kits Enable Precision-Guided Forensic Analysis of Highly Compromised Human Samples