Background Cellular immunity is dependent on T-cell recognition of peptide/major histocompatibility complex (MHC) and is a critical molecular recognition component [1]. A large class of bioinformatics tools facilitates the identification of T-cell epitopes to specific MHC alleles. However, not all peptide residues contribute equally or are relevant to binding due to polymorphism of genes encoding MHC, making development of statistical methods difficult. Information Theory has proved to be one of the most universal mathematical theories that governs virtually all processes [2]. The success of this approach in analyzing a huge range of engineering, technological and natural processes is impressive. In Molecular Biology the applications have been very successful at the sequence level, many sequence comparison and binding site identification methods now boasts a sound information theoretic foundation.
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