Helixir Genomics
Live longer, and better, a longevity plan from your DNA.
Your DNA already holds clues about how you age, what fuels you, and how your body responds. A precision medicine analyst reads yours by hand, and nothing is written down until it has been checked back against your own raw data. What you get is a few clear changes, the ones that actually help you live longer and better.
- bases in your genome
- 3,000,000,000
- read end to end, about thirty times over, at the whole-genome depth
- positions typed by a DNA array
- 680,000
- the best-studied ones, extended by inference to millions
- genes screened for inheritance
- 3,572
- each one measured against your own sequence, not a panel name
- person reads it, by hand
- 1
- a precision medicine analyst, one genome at a time
Why it matters
You were born with a set of patterns. They are not your fate.
How you age, what gives you energy, how your body handles food, drink, sleep, training and the medicines you may one day take, a lot of it is written in your DNA. Read early, it tells you where your attention is worth the most, while small changes still add up.
We read it carefully, against the latest science, and explain it in plain language, not a list of variants, but a few things you can actually do. You can follow exactly how we read your DNA at every step.
Your Precision Longevity Analysis
Every area, included.
There is no menu and no upsell: every analysis covers all eight areas at one flat price, and your questionnaire tells us where to go deepest. Each area is explained simply: what your DNA shows, and what you can do about it. Couples can be read together, which adds what a future child could inherit. See what each area covers in full.
- 01
Long-term health
Heart, brain, metabolism, hormones: where your DNA raises or lowers your odds for the conditions that shape long lives. Knowing where you lean lets you act early, while it still counts.
What this area covers - 02
Inheritance
What you carry without knowing, and what a child of yours could inherit. With whole-genome sequencing we screen 3,572 genes and tell you, gene by gene, how confident the answer is.
What this area covers - 03
Pharmacogenomics
How your body handles common medicines, on a cut-out card sized for your wallet. Hand it to any physician about to write you a prescription, so the dose is an informed choice from the start.
What this area covers - 04
Fitness & performance
The training your biology actually rewards, where recovery needs more room, and the joints and tissues worth protecting before they complain.
What this area covers - 05
Nutrition, food, drink, sensitivities
Caffeine, alcohol, lactose, gluten, salt: what suits you and what does not. Small daily choices tuned to your biology instead of a population average.
What this area covers - 06
Personal supplementation plan
A short, reasoned list of what is worth taking for your body, with doses and the food that would do the same job, and an honest account of what to stop.
What this area covers - 07
Ancestry & deep lineages
Where you come from, traced along your maternal line and, if your DNA carries a Y, your paternal one. The deep context every other finding is read against.
What this area covers - 08
Longevity screener
Our age-and-ancestry-adjusted screener across the conditions that shape long lives, drawing the other seven areas into one considered view of how you are aging.
What this area covers
What changes for you
Understanding, you can act on.
The value is not the document. It is what you do differently once you see yourself clearly, the controllable things, brought forward while they still matter.
- 01
A personal longevity plan
A few clear changes, chosen for your biology rather than generic advice. Start now, and return to it as the years pass.
- 02
How your body handles medicines, on record for life
If a doctor ever considers a prescription, the right drug and the right dose can be matched to how you are built.
- 03
What to eat, train and supplement for your biology
How you respond to food, drink, sleep and exercise, and what is genuinely worth taking, tuned to you and not to someone else.
- 04
What to flag with your doctor, early
Anything worth a medical conversation, surfaced clearly, with honest notes on what is known and what is not.
Who it is for
For people who feel well and intend to stay that way.
This is prevention by design, not a reaction to illness. If you are healthy and want to understand your body while your choices still compound, this is written for you. The earlier you start, the more those choices are worth.
How yours is made
Read by a person, not an algorithm.
Most DNA companies run your data through software and hand back a report in seconds: one template, the same for everyone, filled with your numbers. Yours is not. A precision medicine analyst, an expert in genetic and genomic analysis, sits with your genome and any bloodwork you share, and reads it against the latest science by hand.
No two analyses are alike. Each one is written from scratch for your case: your biology, your questions, what you asked us to look at. It is closer to a private consultation with a scientist than to a product, and it takes days, not seconds, because a plan worth following has to be built for one person, you, and no one else. Here is why a person, not an algorithm, and how your analysis is made, step by step.
Read by
A precision medicine analyst
Every analysis
Written from scratch for you
Every finding that matters
Checked back against your raw data
What you receive
A plan you keep returning to.
You get a personal longevity plan, the few changes that matter for you, and the findings worth carrying forward. It arrives as a printed volume, with a digital edition, made to be read once and returned to as your life and your biology change.
Area 01
Long-term health.
Where your DNA quietly raises or lowers the likelihood of the conditions that shape long lives.
Eleven findings worth your attention across the cardiovascular, metabolic, neurological and endocrine domains. Read with the understanding that direction is not destiny.
Written for E. M. · February 2026
Finding 01 · cardiometabolic
Lipid handling, moderately raised LDL trajectory
Three independently studied variants in your file (APOE, LDLR, PCSK9) sit on the side that raises lifetime LDL more than average, small effects each, modest in combination. Worth a periodic lipid panel; not, on its own, a reason for medication.
¹ Sources: Khera 2018 (NEJM); Klarin 2018 (Nat Genet); Sniderman 2019 (JACC). Full citations · pp. 102–104.
How deep to read
You choose how deep we read.
The interpretation is the same either way, read personally by the same precision medicine analyst. What you decide is how much of your DNA there is to read.
Both depths cover the same eight areas, at one flat price each. The difference is how much of your DNA is read, and what that reach makes possible.
One genome, start to end
Chosen positions, and the gaps between them. The hollow marks are rare variants the array has no probe for.
On your data
Your genome is yours. Never sold, never shared for advertising or research, never used to train anything. Encrypted at rest, encrypted in motion, and removed on request.
Begin
The life ahead of you, written for you.
Tell us what you would like to understand. It starts a short consultation, then a precision medicine analyst writes back with a personal proposal: what your analysis would cover, and the terms.
Your analysis is not a diagnostic test. It is informational and educational, written to be read, considered, and brought to a physician where it matters.