Did you find it to be more insightful than partial sequencing like 23&Me? What did you learn?
To be honest, neither test produced much usable information. The whole genome produces more results, but I don’t really have anything of great significance in either output.
This seems to be common. The few genome interpretation groups I’ve looked at are full of people trying to extract significant meaning from results that don’t really say much.
Unless you have a major genetic problem, the results of any of these tests aren’t hugely helpful. It’s also too easy to misinterpret the results and think that some of them are more significant than they really are. Most individual genes don’t have a huge effect on overall health, despite what some of the unscrupulous genome analysis sites try to sell you.
Bugs everywhere but things mostly don’t crash
https://www.nih.gov/news-events/news-releases/nihs-all-us-re...
Make sure to read fine print. Most companies are selling a copy of your DNA to pharma, which is how they keep cost approachable.
Also, most risk scores are for northwest europeans.