The validation of multiplex solid-phase fluorescent minisequencing of mitoc
hondrial DNA (mtDNA) for use in forensic casework is presented. Validation
included testing of the reliability and species specificity of the techniqu
e, analysis of mixed body fluid samples, analysis of samples and substrate
controls from previous cases and somatic stability of mtDNA. Animal, bacter
ial and fungal species extracts were examined and the test did not show cro
ss-reactivity with other species. Hair, blood, saliva, faeces and semen or
vaginal samples were tested from five male and five female individuals. For
all the samples tested, heteroplasmy was observed only at position 302/309
.1. Body fluid mixtures (blood:saliva, semen:saliva, faeces:semen, vaginal:
semen) and DNA:DNA mixtures were examined. in total, 189 mixtures were anal
ysed of which one resulted in a hybrid profile consisting of peaks from eac
h of the two donors. The semen fraction of the semen:saliva and vaginal:sem
en mixtures appeared to be concentrated in the supernatant fraction of the
extract thus highlighting the need to extract both the pellet and supernata
nt fractions of a stain. Control samples, crime stains and their substrate
controls from previous cases were examined. Of the 12 loci typed by miniseq
uencing, 11 could be verified by comparison to results from the sequencing
method currently in use for casework and no discrepancies were observed bet
ween the two. MtDNA minisequencing was found to be a reliable and reproduci
ble technique and its rapid and discriminating nature make it particularly
suitable as a screening technique.