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The performance of a random library should give us a lower bound on
the fitness of evolved libraries, given that I start the
simulation with random antibody libraries. I therefore derived the
expected fitness of a random library on the complete pathogen set of
size 2L. Let
be the score of an individual with
respect to pathogen pi and m the number of matching bit positions
between a pathogen and an antibody. For a pathogen binding to a single
random antibody, the probability that there are x or fewer matching
bits,
,
is given by the value of the cumulative
binomial at x. If we have A random antibodies, the probability
that all of them have x or fewer matching bit positions with the
pathogen is
.
Then the probability
that the score
of the individual with respect to pathogen
pi is x/L, is given by the probability that at least one antibody
has x matching sites with the pathogen but none has more than x,
i.e.,
The expected score of a random
library of A antibodies with a random pathogen pi is then given
by
The expected score of a random library on a randomly chosen pathogen
pi also represents the expected score of a random library over the
complete set of 2L pathogens. We then denote the expected fitness
of a random library over the complete pathogen set by fr,
![\begin{displaymath}f_r = E[\phi(p)] = \frac{1}{L} \sum_{x = 0}^L x \left[Pr\{m \leq x\}\right]^{A} -
\left[Pr\{m \leq x-1\}\right]^{A}.
\end{displaymath}](img24.gif) |
(2.1) |
The above equation for fr gives a lower bound on the fitness of the
evolved libraries as a function of L and A.
Next: Upper bound on the
Up: Shape space coverage with
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Mihaela Oprea
1999-04-11