Pharmacogenetics: The Right Drug, the Right Dose
Genetic differences change the effect and side-effect risk of many drugs. Pharmacogenetic tests help personalize treatment choice and dosing.
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NIPT: Screening the Baby's Chromosomes from the Mother's Blood
Non-invasive prenatal testing (NIPT) screens for common chromosomal abnormalities from cell-free fetal DNA in the mother's blood from the 10th week of pregnancy.
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Hereditary Cancer Panels: Who Are They For?
About 5 to 10% of all cancers are hereditary. Genetic panels identify the mutations that raise risk based on personal and family history, guiding follow-up and prevention plans.
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What Is Preimplantation Genetic Testing (PGT)?
PGT allows embryos to be examined for specific genetic conditions before they are transferred to the uterus during IVF.
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Diagnosing Rare Diseases with Whole Exome Sequencing (WES)
The exome is the protein-coding part of the genome, and most disease-causing variants are found there. WES is a powerful tool for undiagnosed rare diseases.
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Carrier Screening: Before Marriage and Pregnancy
Healthy individuals can unknowingly be carriers of recessively inherited diseases. Preconception screening gives couples the opportunity to plan with full knowledge.
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The Role of Genetic Counseling in the Diagnostic Process
Genetic counseling is an integral part of testing: choosing the right test, communicating the result clearly and involving family members in the process.
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Test Preparation Guide and E-Results System Now Live
The fasting, medication and timing rules to follow before giving a sample, along with the steps for accessing results online, have been compiled in the Knowledge Center.
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