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tion scheme for obtaining random samples of the posterior distribution of the imputed
parameters of the model. In Section 3.5, we discuss the criterion to select the peptides
that bind with high affinity to certain tissues. We perform a simulation study to asses
further the properties of our model and our peptide selecting criterion in Section 3.6.
In Section 3.7, we show the results of applying our model to the human three-stage
phage display experiment. Finally, we provide some concluding remarks in Section
3.8.

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