Analysis of somatic mutations in V regions of Ig genes is important for und
erstanding various biological processes. It is customary to estimate Ag sel
ection on Ig genes by assessment of replacement (R) as opposed to silent (S
) mutations in the complementary determining regions and S as opposed to Ii
mutations in the framework regions. In the past such an evaluation was per
formed using a binomial distribution model equation, which is inappropriate
for Ig genes in which mutations have four different distribution possibili
ties (R and S mutations in the complementary-determining region and/or fram
ework regions of the gene). In the present work, we propose a multinomial d
istribution model for assessment of Ag selection, Side-by-side application
of multinomial and binomial models on 86 previously established Ig sequence
s disclosed 8 discrepancies, leading to opposite statistical conclusions ab
out Ag selection. We suggest the use of the multinomial model for ail futur
e analysis of Ag selection.