The signs and symptoms of genetic diseases can have certain complications, so that in many cases, the definitive diagnosis of rare genetic diseases is difficult. Today, with the advancement of technology and the use of new methods known as ultra-precision medicine, effective steps can be taken in more targeted medical decisions and thus reducing the probability of future children of the family suffering from genetic diseases.
Therefore, by using the knowledge and experience of a specialized team, we produced and developed Whole Exome Sequencing (WES). WES is a diagnostic test that identifies pathogenic mutations in exons by sequencing the patient's entire exons and analyzing the statistical results based on artificial intelligence and finally by using precise genetic analysis.
