تسلسل الجينوم الكامل - Duo

This full genome sequencing test aims to identify gene sets that may help diagnose patients with rare genetic disorders by analyzing all protein-coding genes (over 18,000) and non-coding genes (over 15,000) in the human genome, detecting single nucleotide variations and small insertions/deletions, copy number variations, and large structural variants.

• The description claims that the test may discover incidental genetic changes of medical importance but not directly related to the primary reason for the genomic test.
• The description claims that Enigma Genomics will notify the policy regarding any incidental results related to adult-onset neurodegenerative disorders for which there are no interventions available.