Whole Exome Sequencing (WES)

Whole Exome Sequencing (WES) is a powerful genetic test that focuses on sequencing the exons, which are the protein-coding regions of your genome. These exons make up less than 2% of your entire DNA but contain about 85% of the genetic variations associated with diseases. By analyzing these crucial regions, Whole Exome Sequencing can identify genetic mutations responsible for various health conditions, making it an invaluable tool for diagnosing rare genetic disorders and understanding complex diseases.

This test provides detailed insights that can guide personalized treatment plans, improve health outcomes, and help prospective parents understand their risk of passing on genetic disorders. Whole Exome Sequencing offers a targeted and cost-effective approach to genetic analysis, providing valuable information that can significantly impact your health and well-being.