In forensic DNA analysis, a DNA extract is amplified using polymerase chain reaction (PCR), separated using capillary electrophoresis, and the resulting DNA products are detected using fluorescence. Sampling variation occurs when the DNA molecules are aliquotted during the PCR setup stage and this translates to variability in peak heights in the resultant electropherogram or between electropherograms generated from a DNA extract. Beyond the variability caused by sampling variation it has been observed that there are factors in generating the DNA profile that can contribute to the magnitude of variability observed, most notably the number of PCR cycles. (Publisher abstract modified)
Downloads
Similar Publications
- Camera-View Augmented Reality: Overlaying Navigation Instructions on a Real-Time View of the Road
- Cognitive and contextual influences in determination of latent fingerprint suitability for identification judgments
- Restoring Promise: Positive Research Results from a Program that Aims to Transform Correctional Culture