DNA analysts in forensic laboratories are engaged in analysing and sampling bloodstains from bloodstained items. Detailed and precise descriptions of bloodstains on items of interest are very important for bloodstain pattern analysis (BPA). DNA and BPA reports were examined from forensic laboratories in Serbia ( = 88). About 400 reports were observed from the past three years. First, we analysed descriptions of items (clothing and shoes) in DNA reports, and special attention was paid to descriptions of bloodstains. Subsequently, we estimated the value of descriptions of bloodstained items of interest in linking specific types of bloodstains to the obtained DNA profiles. Observed descriptions of bloodstained items in DNA reports are usually limited to phrases. A major problem exists in cases where several people were injured in the same bloodshed event. Connecting specific types of bloodstains to obtained DNA profiles is essential for the reconstruction of crime events. The complete analysis should therefore include detailed descriptions of all types of observed and sampled bloodstains. In DNA laboratories that are within a larger institute, it would be more appropriate and productive if BPA and DNA experts examined bloodstained items cooperatively. Moderately sized laboratories have a limited number of employees. So, in those DNA laboratories, it would be more appropriate to educate DNA analysts in the basic principles of BPA.
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http://dx.doi.org/10.1177/0025802420926876 | DOI Listing |
Forensic Sci Int
August 2024
Department of Forensic Medicine/Medical Jurisprudence, University of Health Sciences, Lahore, Pakistan. Electronic address:
Criminals often attempt to conceal blood-stained weapons used in violent crimes, making forensic evidence crucial in solving cases. This study explores the recovery and extraction of trace DNA from sports equipment, including cricket bats, table tennis racquets, and hockey sticks, which are frequently implicated in such incidents. Our research evaluates various double swab collection methods for retrieving trace DNA from these sports items, emphasizing those associated with blunt force trauma.
View Article and Find Full Text PDFMed Sci Law
October 2020
The Institute of Forensic Medicine Nis, Faculty of Medicine, University of Nis, Serbia.
DNA analysts in forensic laboratories are engaged in analysing and sampling bloodstains from bloodstained items. Detailed and precise descriptions of bloodstains on items of interest are very important for bloodstain pattern analysis (BPA). DNA and BPA reports were examined from forensic laboratories in Serbia ( = 88).
View Article and Find Full Text PDFLeg Med (Tokyo)
May 2019
Department of Forensic Science, College of Criminal Justice, Sam Houston State University, 1003 Bowers Blvd., Huntsville, TX 77340-2525, United States; School of Biomedical Sciences, University of Queensland, St. Lucia, QLD 4072, Australia.
The identification of body fluids in evidentiary stains may provide investigators with probative information during an investigation. In this study, quantitative reverse transcription polymerase chain reaction (RT-qPCR) assays were performed to detect the presence of mRNA and miRNA in fresh and environmentally challenged samples. Blood, semen, and reference markers were chosen for both mRNA/miRNA testing.
View Article and Find Full Text PDFForensic Sci Int Genet
September 2014
Forensic Science Service Tasmania, 20 St. Johns Avenue, New Town, Tasmania 7008, Australia.
A significant number of evidence items submitted to Forensic Science Service Tasmania (FSST) are blood swabs or bloodstained items. Samples from these items routinely undergo phenol:chloroform:isoamyl alcohol organic extraction and quantitative Polymerase Chain Reaction (qPCR) testing prior to PowerPlex(®) 21 amplification. This multi-step process has significant cost and timeframe implications in a fiscal climate of tightening government budgets, pressure towards improved operating efficiencies, and an increasing emphasis on rapid techniques better supporting intelligence-led policing.
View Article and Find Full Text PDFJ Hosp Infect
February 1988
Hospital Infection Research Laboratory, Dudley Road Hospital, Birmingham.
The choice as to which of the two gaseous processes is best suited to individual hospital needs is a difficult one. Very few items are unable to tolerate 73 degrees C (LTSF) and these few can withstand 37 degrees C or 55 degrees C (EO). Unfortunately, LTSF is a 'moist' process and sterilizers have a poor history of providing sterilization without modification, and consequently few are used.
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