Cellgenetics

We are a leading laboratory for genetic testing, dedicated to providing accurate, reliable, and innovative genetic testing services to individuals, healthcare providers, and researchers. We offer a wide range of genetic tests, including whole-genome sequencing in different fields of medicine (cancer, cardiovascular diseases, neurology, reproductive health, etc.), carrier screening, invasive and non-invasive prenatal testing (NIPT), lifestyle, and pharmacogenomics testing. Our team of highly trained and experienced professionals is committed to advancing the field of genetics through ongoing research and development, and we strive to provide our clients with the most up-to-date and clinically actionable information. We rely on thorough genetic counseling to provide the most informative and suitable test for each client regarding disease prevention, diagnosis, and treatment. Our laboratory specializes in bioinformatic analysis of whole-genome sequencing data and its interpretation by all internationally acclaimed standards and guidelines. Whole-genome sequencing decodes 100% of the DNA in a person’s cell. It is the most comprehensive DNA test and allows targeted bioinformatic analysis of any gene/genes associated with various diseases. We offer the most extensive neonatal/toddler diagnostic test screening the baby's genome for early-onset childhood diseases. We offer a wide range of NIPT tests, including one of the most informative NIPT tests to date, thus enabling parents and doctors to choose the most suitable test for every pregnancy. In genetic testing, everything matters.