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The aim of this research is to automate an analysis of the EGFR gene as a whole, and especially an analysis of those exons with clinically identified microdeletion mutations which are recorded with non-mutated nucleotides in a long chains of a, c, t, g nucleotides, and “-“ (microdeletion) in the NCBI database or other sites. In addition, the developed system can analyze data resulting from EGFR gene DNA sequencing or DNA extraction for a new patient and identify regions potential microdeletion mutations that clinicians need to develop new

the international journal of computational intelligence systems/international journal of computational intelligence systems

EGFR Microdeletion Mutations Analysis System Model Using Parameters Combinations Generator for Design of RADBAS Neural Network Knowledge Based Identifier