Whole Exome Sequencing (WES)

Discover variants in exonic regions

Whole exome sequencing (WES) is a powerful method that provides high-resolution genetic information of the protein-coding regions in a genome, called exons. The human genome consists of about 180,000 exons, which are specifically selected with special kits and sequenced with NGS. This allows the identification of protein-altering genetic variants at a fraction of the cost for whole genome sequencing.

We will be happy to complete your WES project with our bioinformatics services for detection, annotation, and pathogenicity assessment of genetic variants.