Whole Exome Sequencing
Reads the protein-coding regions of your DNA, the parts most closely linked to health and disease, to help identify the specific gene changes behind symptoms or a suspected rare genetic condition, using your sample alone.
Reads the protein-coding regions of your DNA, the parts most closely linked to health and disease, to help identify the specific gene changes behind symptoms or a suspected rare genetic condition, using your sample alone.
In most cases, a simple blood draw is all it takes. Your physician will confirm the exact method for the test or tests you choose.
Between 10 and 30 days, depending on the test. Simpler panels come back faster; the more comprehensive tests, like Whole Genome Sequencing, take longer to process.
Yes, we recommend it. A short consultation with your physician will help you choose the tests most relevant to your goals and health history.
Yes. Every result is reviewed with you by a physician, who explains what it means and what to do with it, rather than leaving you to interpret raw genetic data on your own.