Forensic genetics can provide information about events at a crime scene and supplement other identification methods through DNA analysis. DNA recovered from a crime scene can potentially identify the perpetrator, while DNA statistical interpretation has a solid scientific foundation despite some subjective interpretations of complex mixtures. DNA also allows for identification through kinship as close relatives can act as reference points, helping to identify missing persons. While PCR gives DNA testing high sensitivity, contamination is also highly possible due to amplification. STR remains the primary method for DNA profiling despite other markers being used for specific applications.
Forensic genetics can provide information about events at a crime scene and supplement other identification methods through DNA analysis. DNA recovered from a crime scene can potentially identify the perpetrator, while DNA statistical interpretation has a solid scientific foundation despite some subjective interpretations of complex mixtures. DNA also allows for identification through kinship as close relatives can act as reference points, helping to identify missing persons. While PCR gives DNA testing high sensitivity, contamination is also highly possible due to amplification. STR remains the primary method for DNA profiling despite other markers being used for specific applications.
Forensic genetics can provide information about events at a crime scene and supplement other identification methods through DNA analysis. DNA recovered from a crime scene can potentially identify the perpetrator, while DNA statistical interpretation has a solid scientific foundation despite some subjective interpretations of complex mixtures. DNA also allows for identification through kinship as close relatives can act as reference points, helping to identify missing persons. While PCR gives DNA testing high sensitivity, contamination is also highly possible due to amplification. STR remains the primary method for DNA profiling despite other markers being used for specific applications.
Information regarding events which occurred at a crime scene or information needed to supplement other methods of forensic identification can be provided through forensic genetics. DNA molecular analysis has been an important method in forensic investigations during the past 30 years and has been able to provide capabilities not found in most of the other forensic methods. DNA recovered from a crime scene is a power tool which can be utilized to potentially identify the perpetrator. DNA statistical interpretation is based on a solid scientific foundation, but interpretations of complex DNA mixture profile can still be subjective and inconsistent under certain circumstances. Another important capability of DNA is the nature of its inheritance pattern which enables the utilization of close biological relatives as reference points. For example, missing persons and disaster victims can be identified through kinship associations (Butler, 2015; Dumache et al., 2016). Forensic DNA testing has superb sensitivity due to amplification of target regions with polymerase chain reaction (PCR). However, the usage of high-sensitivity techniques also means that contamination from other DNA not associated with the crime sample is highly possible. Currently, the method used in DNA profiling is based on the short tandem repeats (STR) which still remains as the primary workhorse in forensic DNA analysis despite the usage of other genetic markers for specific applications. In the last decade, new biomarkers such as microRNAs (miRNA), messenger RNA (mRNA), and DNA methylation have been studied and proposed to be utilized in the forensic identifications (Butler, 2015; Dumache et al., 2016). Butler, J.M. (2015), “The future of forensic DNA analysis”, Philosophical Transactions of the Royal Society B: Biological Sciences, Vol. 370 No. 1674, available at:https://doi.org/10.1098/rstb.2014.0252. Dumache, R., Ciocan, V., Muresan, C. & Enache, A. (2016), “Molecular DNA Analysis in Forensic Identification.”, Clinical Laboratory, Verlag Klinisches Labor GmbH, Vol. 62 No. 1–2, pp. 245–248.