Pitfalls in the Genetic Identification of Human Remains
Journal Title: Peer Reviewed Journal of Forensic & Genetic Sciences - Year 2018, Vol 1, Issue 2
Abstract
DNA technology is an irreplaceable tool for the identification of human remains, but the reliability of the ante mortem reference data remains a serious concern. We present here two cases where misleading conclusions could be achieved by using only the genetic profile of the missing person's father such as reference sample. Nevertheless, when appropriate reference DNA samples (e.g., the maternal samples) became available, certain identifications were achieved as shown by the probability of maternity (> 99.999%). Thus, all these data together show that extra-pair paternity was found by the way, in both cases. Precautions to avoid misleading conclusions are addressed. From the beginning of PCR era it rose that DNA profiling of human remains could be an irreplaceable tool for personal identification. Now, after two decades, DNA technology represents the golden standard for human identification, which is being used even for mass disaster and mass graves victims. DNA testing is, by definition, a sample-to-sample comparison, and its reliability in the identification of human remains depends from several factors, out of them the degradation of the sample and the availability of the "ante mortem reference data" (AMRD) play the major role.
Authors and Affiliations
Consoloni Lara, Recchia Elisa, SorçaburuCilieri Solange, Gobbo Chiara, Fattorini Paolo, Edalucci Elisabetta
Ludopathy: Play to Lose
This is a relatively new concept, and if you do not know what it is about, dear reader, I will ask you the following: please go at about 10.45 in the morning to a place that has among its premi...
Features and Prospects of Development of The Labor Market in Uzbekistan
There are different approaches on determining the object that causes of buying-selling interactions in labor market. Discussions about labor market has been continuing since the middle of the last century. I...
Whole-Exome Sequencing Reveals a Recurrent D401N Mutation in the COMP gene that Causes Multiple Epiphyseal Dysplasia
Multiple epiphyseal dysplasia (MED) is a rare osteochondrodysplasia characterized by moderate short limb dwarfism and early-onset osteoarthrosis. By whole-exome sequencing (WES), we identified a dominantly inherited muta...
Rett Syndrome: Reporting A Case and Review in Literature
Rett syndrome is a disorder in children’s neurological development characterized by an initial normal evolution followed by the loss of voluntary use and characteristic movements of the...
Critical Exploration of Counselor Client Relationship in Disability and Gender -Case Study
This study examines the working experiences of the counselors and their relationship with their clients. There are two types of clients chosen for this study: clients with intellectual disability and the clients of oppos...