Frequently asked questions
What is precision medicine / applied genomics?
Precision medicine is an approach that uses each patient's genetic, molecular and clinical information to personalize prevention, diagnosis and treatment, rather than applying the same protocol to every patient. Applied genomics studies DNA and its variants to understand disease risk, treatment response and prognosis.
Who is this service for?
This service is for patients who already have the results of a genetic or molecular test and need specialized interpretation, treating physicians seeking a scientific second opinion, and institutions, laboratories or research groups that need guidance in oncogenomics or biomedical project design.
Do you collect the sample or perform the laboratory test?
No. The center does not collect biological samples or perform laboratory processing. Our work is to interpret molecular results already generated by a certified laboratory, translating those findings into a clear, applicable scientific report.
What happens to my genetic data? How is my information protected?
Your genetic and clinical information is handled confidentially, in accordance with our Data Policy. We do not share your results with third parties without your authorization, and data is used exclusively to prepare the requested report. You can review the full details on our Data Policy page.
How much does the service cost?
The cost varies depending on the type of interpretation or consulting you need. You can see the full, up-to-date details on our Pricing page.
How long does it take to receive the report?
Delivery time depends on the complexity of the case and the type of analysis requested. We confirm this directly when you book your consultation or submit your request, so you get a realistic timeframe for your specific case.
Do I need a referral from my doctor, or can I consult directly?
You can contact us directly without needing a referral. However, we recommend that your treating physician be aware of the consultation and, when possible, take part in the conversation, since they know your complete medical history and are the one who should make management decisions together with you.
I already had a genetic test done elsewhere. Can you still help me interpret it?
Yes. In fact, that is one of the center's main services: interpreting molecular results already generated by another laboratory, explaining their clinical meaning and relevance to your case.
Does this service replace my treating physician?
No. This is a scientific consulting and interpretation service that complements, but does not replace, your relationship with your treating physician. Diagnosis and treatment decisions should always be made together with the healthcare professional managing your case.
What happens if the result is inconclusive or a "variant of uncertain significance" (VUS)?
This is a common finding in genetics: a variant of uncertain significance (VUS) means that, based on currently available scientific evidence, it cannot be classified as either benign or disease-causing. In these cases we explain what the finding actually means, what options exist (such as future reassessment as more evidence becomes available), and what cannot yet be concluded from that result.