Forensic applications of DNA typing data require the estimation of the
frequencies of all observed alleles, which is currently done by a fix
ed set of groupings (binning) of alleles in a database. Recently it's
validity has been questioned on the ground that when a DNA fragment si
ze is close to a bin boundary, the frequencies of all adjacent bins sh
ould be added. On the contrary, the current forensic database indicate
s that when the match window of a DNA fragment overlaps 2 bins, it is
enough to consider the bin with the larger frequency, and this never u
nderestimates the frequency within the match interval with the current
choice of fixed-bin widths. On average, the current fixed-bin procedu
re yields an allele frequency at least 2-fold higher than that of a fl
oating-bin.