How you should be sleeping.
Are you really bad at waking up in the morning? Find out when your optimal sleep times are, how you process caffeine, and how to secure the best night of sleep, every night.
myfiftyone sequences your whole genome and tells you what to do, not just what your DNA says.
Your data is never sold, never shared, or used to train AI models.
Are you really bad at waking up in the morning? Find out when your optimal sleep times are, how you process caffeine, and how to secure the best night of sleep, every night.
Learn why one glass of milk makes you feel bloated, what your alcohol tolerance really is, and if cashews are behind your tiredness. Everyone’s body reacts differently to different foods. Learn what is optimal for you.
Guidelines are written for populations, but health should not be one-size-fits-all. Learn what is unique about yourself and what you should change as a result.
A kit arrives in a few days. Saliva, no needles, no clinic. Post it back in the prepaid envelope.
Your sample is processed by an accredited sequencing lab at 30x whole genome coverage. Results in about four weeks.
Our state of the art AI systems constantly scour the latest research to keep up to date. We use this to create an in-depth report on the areas you care about.
You can ask our system questions any time, and it will use the latest research to give you the best answer. So if you are wondering why you feel tired, or what exercises you should be doing, just ask. You will get answers grounded in the latest research, tailored to you.
Not to advertisers. Not to insurers. Not to pharmaceutical companies. Not to data brokers. There is no research partnership tier you get opted into by default.
One click, any time, no retention window, no phone call to cancel. Your sample is destroyed, and your sequence is erased from primary and backup storage. We will confirm in writing when it is done.
Export your raw sequence file whenever you want. It is your genome, and you should be able to walk out with it.
myfiftyone is a health and wellness product, not a diagnostic. When we surface something that warrants clinical follow-up, we say so directly and give you a summary to take to your doctor rather than burying it in caveats.
Sequencing is performed by an accredited laboratory at 30x coverage, the depth used for clinical whole-genome work. Interpretation is based on peer-reviewed literature and clinical variant databases, and we tell you the strength of evidence behind every finding.
About four weeks from posting your sample.
Yes, any time, in standard formats.
Delete everything with one click. No retention period, no exceptions.
We are opening in small batches so every early member gets real attention.
Your data is never sold, never shared, or used to train AI models.