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