A wide range of genetic tests are performed at ECEGEN to diagnose and prevent hereditary diseases that may occur at any stage of life, starting from the pre-pregnancy process. We guide you to the most accurate diagnosis in the shortest time with our advanced technology, international accreditation, and expert physician interpretation.
Our Main Test Categories
- Next-Generation Sequencing (NGS) Panels and Whole Exome (WES): Analysis of all protein-coding regions or targeted gene panels to identify rare and undiagnosed conditions.
- Prenatal and Postnatal Karyotyping (Cytogenetics): Cell culture studies performed to detect deviations in chromosome number and structure.
- NIPT (Non-Invasive Prenatal Testing): Screening for chromosomal abnormalities such as Down syndrome from maternal blood.
- Preimplantation Genetic Testing (PGT): Screening of embryos for chromosomal or single-gene disorders before transfer in IVF treatments.
- Cancer Genetics & Carrier Screenings: Susceptibility testing for hereditary breast, ovarian, colon cancers, and carrier screening for couples (e.g., SMA).