New Technology Applied to Clinical Diagnosis


Our medical laboratory at Sofiva Genomics is led by an integrated team of R&D professionals, lab technicians, bioinformatics analysts, database specialists, and clinicians, all working together to promote clinical research and application of genomics within the context of preventative medicine. The laboratory is fitted with the latest and most efficient equipment for performing next-generation sequencing (NGS), array scanning, nucleic acid sequencing, high-performance capillary electrophoresis, fluorescent capillary electrophoresis, high-performance liquid chromatography, high-resolution melting, polymerase chain reaction analysis, and automated DNA extraction.

Our gifted team of R&D and technical specialists are at the forefront, both locally and internationally, of developing diagnostic platforms to read genes associated with spinal muscular atrophy, neonatal sensorineural hearing loss, and congenital central hypoventilation syndrome. Their work also includes testing gene array and conducting preimplantation genetic diagnosis, NGS for PGS, and NIPS+, as well as customized personal genetic testing services. At Sofiva, we are committed to offering services which are both compassionate and comprehensive.

Genomics Laboratory

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