Twenty-seven samples (cell cultures prepared for routine cytogenetics)
of leukemia patients with known cytogenetic abnormalities were staine
d by in site hybridization for interphase cytogenetics with centromere
specific probes for chromosome Nos 4, 6, 7, 8, 9, 12, 17, 18, X and Y
. The number of hybridization domains per nucleus was quantified using
a semi-automated system developed in our laboratory. Results of this
automated counting procedure (with and without verification of the cou
nting results by the operator) were compared with conventional cytogen
etic data and with visual scoring of the number of hybridization dots.
The findings show that the system is capable of analysing 1000 cell n
uclei in less than 30 min, including the necessary verification of the
results by the operator. Automated counting and visual scoring were i
n good agreement. Conventional cytogenetics and interphase cytogenetic
s agreed in only 50% of the cases, confirming other studies showing th
at conventional cytogenetic results are not always representative for
the majority of the cell population.