The European DNA Profiling Group (EDNAP) has previously carried out co
llaborative exercises to determine which STR systems will produce resu
lts that can be reproduced by different laboratories. The first EDNAP
exercise involving STR systems focused on different types of loci: a s
imple locus with six common alleles (HUMTHO1) and a complex locus with
>35 alleles (ACTBP2). Generally the simpler STR system was found to b
e readily amenable for use across a wide range of different technologi
es, whereas a more complex locus presented difficulties. The second ED
NAP STR exercise was intended to take the process of investigation a s
tage further. Some laboratories are developing automation, coupled wit
h fluorescent methods of detection and multiplex applications, whereas
others use manual methods involving visual detection techniques such
as silver staining. The purpose of this exercise was to determine whet
her loci amenable to multiplexing with automation (as a quadruplex rea
ction) could also be successfully used with manual methods, either by
multiplexing in duplex reactions or alternatively by using just a sing
le pair of PCR primers.