Our view
We focus on interpretation and context, not genetic horoscopes. The same DNA is present in many cell types, and a change may matter in some of them and not others.
Sequence data only becomes useful when it is read carefully and placed in a clinical setting: what a change may mean, in which tissues or cell types, and whether that information can actually guide care.
01
Interpret
What a change in the sequence may mean, read with care rather than guesswork.
02
Context
Which tissues and cell types a change affects, and which it leaves alone.
03
Clinical use
Whether the finding can genuinely guide a decision about someone’s care.
The limits we keep in view
- A sequence is information. It is not a medicine.
- Interpretation is uncertain, and findings can change as evidence grows.
- Genetic data is sensitive and is handled only with clear consent.