تسلسل الجينوم الكامل - تريو

This full genome sequencing test evaluates all protein-coding genes (over 18,000) and non-coding genes (over 15,000) in the human genome, identifying single nucleotide variations and small insertions/deletions, copy number variations, and large structural variants. It includes routine case-level reanalysis every 6-12 months for up to two years.

• The description claims that the test may identify medically important genetic changes unrelated to the primary reason for the genome test.
• The description claims that Enigma Genomics will notify of any incidental results related to adult-onset neurodegenerative disorders for which there are no interventions.