Determining the source of equine bloodstains by dinucleotide repeats.
Abstract: A novel multiplex of independent dinucleotide tandem repeat (DTR) loci was previously described that is capable of not only discriminating human and equine DNA, but of identifying a single equine source. We report a case in which a bloodstained syringe and two needles were found during inspection of a barn by inspectors of the Pennsylvania Racing Commissions. Using the multiplex and single-locus detection, all 21 equine DTR markers were detected in a suspect horse and two evidence samples, indicating the evidence samples came from the suspect animal. Only six markers were detected in the third evidence sample because the volume of blood was limited. Following whole-genome amplification and single-locus PCR, the third evidence sample detected a total of 17 markers and the likelihood of identity (probability from suspect horse/probability from a random pacer) was 7.0 × 10⁶. The DTR multiplex has some technical limitations, but it is already practical for casework.
© 2010 American Academy of Forensic Sciences.
Publication Date: 2010-06-11 PubMed ID: 20533984DOI: 10.1111/j.1556-4029.2010.01466.xGoogle Scholar: Lookup
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- Case Reports
- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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The research paper presents a case study that used a unique system of identifying horse DNA to track the source of equine blood found at a crime scene.
Objective of the Study
The research primarily focuses on determining the source of horse blood using a novel multiplex of independent dinucleotide tandem repeat (DTR) loci. This system is capable of distinguishing human DNA from equine DNA and identifying a single source of horse DNA.
The Case Study
- The setting of the study involves a barn that was inspected by the Pennsylvania Racing Commissions. A bloodstained syringe and two needles were found at the scene.
- The suspects for the source of the blood included a range of horses, one of which was identified as a potential source. The suspected horse was examined for the 21 equine DTR markers, which are specific segments of DNA that can be tracked.
- All 21 equine DTR markers were found in the suspect horse and two of the evidence samples, suggesting that these samples had come from the suspected horse.
Limitations and Findings
- Only six of the markers were detected in the third piece of evidence, which could be due to the sample having a limited volume of blood.
- In order to extract more information, the researchers performed a whole-genome amplification and single-locus PCR, which is a method of making multiple copies of a specific piece of DNA. This process detected a total of 17 markers from the third sample.
- The probability of the third sample belonging to the suspect horse (as opposed to a random horse of the same breed) was calculated to be 7.0 × 10⁶, a likelihood that significantly implicates the suspect horse as the source.
- Although the process has some technical limitations, the researchers conclude that this DTR multiplex method is already practical for use in investigations concerning equine blood samples.
Cite This Article
APA
Chen JW, Uboh CE, Soma LR, Li X, Guan F, You Y, Liu Y.
(2010).
Determining the source of equine bloodstains by dinucleotide repeats.
J Forensic Sci, 55(6), 1610-1614.
https://doi.org/10.1111/j.1556-4029.2010.01466.x Publication
Researcher Affiliations
- University of Pennsylvania School of Veterinary Medicine, New Bolton Center Campus, 382 West Street Road, Kennett Square, PA 19348, USA.
MeSH Terms
- Animal Welfare
- Animals
- Blood Stains
- DNA / isolation & purification
- Dinucleotide Repeats
- Electrophoresis, Capillary
- Gene Frequency
- Genome
- Genotype
- Horses / genetics
- Humans
- Likelihood Functions
- Needles
- Polymerase Chain Reaction
- Sequence Analysis, DNA
- Species Specificity
Citations
This article has been cited 1 times.- Chen JW, Uboh CE, Soma LR, You Y, Jiang Z, Li X, Guan F, Liu Y. Identification of sample donor by 24-plex short tandem repeat in a post-race equine plasma containing dexamethasone. Springerplus 2014;3:94.
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