The Whole Exome Sequencing test analyzes the Exome – all the exons present in the human genome – 22,000 genes – almost all of the genes involved in rare genetic diseases.
Test results are analyzed against an in-house developed database of more than 15,000 clinical cases of rare genetic disease diagnoses combined with the expertise of our Bioinformatics from international laboratories.
Please contact CHEK Genomics via hotline and email or leave your information in the registration form. Our specialist will contact you as soon as possible.