Clinical exome sequencing and analysis
The human genome is composed of approximately 1-2% exome or coding region of the genome. It accounts for approximately 85% of disease-causing pathogenic variants.
With clinical exome sequencing and analysis, all exons in the human genome are subjected to sequence analysis and have a great deal of importance in putting the definite diagnosis of the disease, especially in unclassified patients.
POLGEN offers fast, reliable and detailed solutions thanks to the new generation of sequencing systems and bioinformatics tools. We are at your service with our information processing capacity, which enables the database to stay in the country and analyzes various databases in the same high resolution and security.
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