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Wera M Schmerer

Publications and source records attributed to Wera M Schmerer.

2 recordsLinked to original sources

Extraction of Human DNA from Soil: Protocol Adaptations

PCR-based analysis of DNA is utilized in a wide variety of fields, including Forensic Science. Aside from the more common ample sources, material analyzed here can refer to specimen excavated from a soil environment, or a sampling of the soil itself to recover DNA leached into the soil from decomposing human remains or from body fluids intermingled with the soil in an outdoor crime scene. The common problematic of these types of sample is the presence of humic acids, which are a component of any soil environment, and when the co-extracted with the DNA, lead to inhibition of enzyme-based procedures including PCR. While a variety of methods exist for the extraction of DNA from excavated skeletal remains, protocols for extraction of DNA from the soil directly are usually targeting soil microorganism. To address the need for methodology suitable for extraction of human DNA from soil, a selection of three published protocols were adapted for this purpose, to be tested and evaluated using standardized samples. The resulting protocols are presented here.

q-bio.QM

Optimized protocol for DNA extraction from ancient skeletal remains using Chelex-100

PCR-based analysis of skeletonized human remains is a common aspect in both forensic human identification as well as Ancient DNA research. In this, both areas not merely utilize very similar methodology, but also share the same problems regarding quantity and quality of recovered DNA and presence of inhibitory substances in samples from excavated remains. To enable amplification based analysis of the remains, development of optimized DNA extraction procedures is thus a critical factor in both areas. The study here presents an optimized protocol for DNA extraction from ancient skeletonized remains using Chelex-100, which proved to be effective in yielding amplifiable extracts from sample material excavated after centuries in a soil environment, which consequently have high inhibitor content and overall limited DNA preservation. Success of the optimization strategies utilized is shown in significantly improved amplification outcomes compared to the predecessor method.

q-bio.QM