Whole Exome Sequencing: Unlocking Answers for Rare and Inherited Diseases
Home > Blogs > Whole Exome Sequencing: Unlocking Answers for Rare and Inherited Diseases What is Whole Exome Sequencing? Whole Exome Sequencing (WES) is a powerful genomic technology that analyzes the protein-coding regions of the genome, known as exons. Although exons comprise only 1–2% of the human genome, they harbor approximately 85% of known disease-causing […]
