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Design of a multiplex PCR for genotyping 16 short tandem repeats in degraded DNA samples

Bibliographic Data

ID5121726
AuthorsFelix Schilz (University of Göttingen), Hummel (0000-0002-3647-8968), Susanne Hummel, Bernd Herrmann (0009-0000-1851-8746)
Year2004
Volume62
Issue4
Pages369-378
Publication date2004-12-16
Open AccessNo
TypeARTICLE
VenueAnthropologischer Anzeiger (JOURNAL)
Journal identifiersISSN: 0003-5548 • E-ISSN: 2363-7099
PublisherS ch we iz er ba rt (PUBLISHER)
DOI10.1127/anthranz/62/2004/369
PMID15648845
OpenAlexW2185975328
LanguageEN

The molecular genotyping of individuals and reconstruction of kinship through short and high polymorphic DNA markers, so-called short tandem repeats (STR), has become an important and efficient method in anthropology and forensic science. The here introduced experimental design describes a multiplex PCR capable of simultaneously amplifying 16 STRs and the sex determinant locus amelogenin in a short fragment lengths range from 84 bp to 275 bp. Thus, the design depends predominantly on the routines for DNA typing of historical samples with highly degraded ancient DNA. It is shown, that the newly designed multiplex PCR is suitable for successful typing of both forensic and historical material.

Allele · Amelogenin · Ancient DNA · Biology · Computational biology · DNA · DNA profiling · Gene · Genome · Genotype · Genotyping · Locus (genetics) · Microsatellite · Multiplex · Multiplex polymerase chain reaction · Polymerase chain reaction · Population · STR analysis · STR multiplex system · Tandem repeat · Typing · Archaeology and ancient environmental studies · Forensic and Genetic Research · Genetics · Medicine · Yersinia bacterium, plague, ectoparasites research

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