“…The visual comparison of the gel of a child with those of its parents, to detect attributes of a child's gel not present in either parent, i.e., a potential mutation, would be extremely demanding, the type of activity guaranteed to lead to a high turn-over rate in technicians. Fortunately, a computer algorithm we had earlier developed for the analysis of protein gels [Skolnick and Neel, 1986] proved suitable, with considerable modification, for the analysis of these complex DNA images [Asakawa et al, 1994]. Among the approximately 2,000 DNA fragments to be visualized on one of these preparations, we identified a subset of approximately 500 for which the coefficient of variation (CV) of spot intensity was Յ0.12, this reproducibility permitting the distinction between spots of normal intensity and spots with 50% intensity with high accuracy (i.e., two-fragment or one-fragment spots).…”