تسلسل الجينوم الكامل - سولو

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

• The description claims that the test may discover 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 policy makers of any incidental results related to adult-onset neurodegenerative disorders for which there are no interventions.