Abstract (EN):
Canine genotyping is demanded in a vast range of situations that more commonly include pedigree verification, parentage and forensic investigations, and population structure, genetic origin and diversity studies. We developed a PCR multiplex that performs consistently up to the standards required for forensic and population analysis. Primers were designed for co-amplification of 9 tetra-nucleotide STR loci in an optimized PCR reaction for fragment size detection in automated capillary electrophoresis. The system includes FH3210, FH3241, FH2004, FH2658, FH4012, REN214L11, FH2010, FH2361 loci (on chromosomes 2, 8, 11, 14, 15, 16, 24 and 33, respectively) and a newly described locus on chromosome 38. Forensic parameters were calculated based on genotyping results obtained in a case-study population. This PCR multiplex for canine genotyping presented robustness and reproducibility of results.
Language:
English
Type (Professor's evaluation):
Scientific
No. of pages:
2