Exome Sequencing

Gentaur Exome Sequencing focuses on the protein-coding regions of the genome, where most disease-related variants are found. Instead of sequencing the entire genome, this method targets exons, giving researchers a cost-effective way to detect mutations that affect gene function. In practice, exome sequencing is widely used in cancer research, inherited disease studies, and clinical genetics to uncover variants linked to health and development. Many labs also apply it for rare disease discovery and population studies. The workflow delivers high coverage, reliable variant calling, and clear data interpretation, helping researchers move from raw DNA to actionable insights with fewer steps.