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Helixir Genomicshelixirgenomics

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 scientist reads yours and turns it into a few clear, practical changes, the ones that actually help you live longer and better.

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

You choose the areas.

Yours is built around the areas you pick. A close look at three is a different study from all seven, and your proposal reflects that. Each area is explained simply: what your DNA shows, and what you can do about it. See what each area covers in full.

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  1. 01

    Disposition

    Where your DNA raises or lowers your odds for the conditions that shape long lives, heart, brain, metabolism, hormones. Knowing where you lean lets you act early, while it still counts.

  2. 02

    Inheritance

    What you carry without knowing, and what a child of yours could inherit. Clear answers, so you can plan with facts instead of guesswork.

  3. 03

    Pharmacology

    How your body handles common medicines. A reference you keep for life, so the right drug and dose can be matched to you, not found by trial and error.

  4. 04

    Lineage

    Where you come from, traced through your maternal and paternal lines. The deep context that every other finding is read against.

  5. 05

    The everyday

    Caffeine, alcohol, sleep, exercise, the foods that suit you and the ones that don't. The daily choices that shape how you age, tuned to your biology.

  6. 06

    Supplementation

    What is actually worth taking for your body, and what to stop. A plan reasoned from your DNA and any bloodwork you share, not a generic stack.

  7. 07

    Together, if you are two

    Couples are read together: what you each carry, what a future child could inherit, and the lineages you would join. For couples planning seriously, whole-genome sequencing reaches the rare variants an array cannot.

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.

  1. 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.

  2. 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.

  3. 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.

  4. 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, the areas you chose. 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

Unique to your case

Automation

Zero

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.

helixir genomicspage 14

Chapter 01

Disposition.

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

page 15chapter 01

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.

LoweredNeutralRaisedHigh

¹ Sources: Khera 2018 (NEJM); Klarin 2018 (Nat Genet); Sniderman 2019 (JACC). Full citations · pp. 102–104.

Read by Adriano De Marino, PhDVol. I

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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.

A DNA array reads the well-studied, pre-selected markers across your DNA, generous and a fine place to begin. Whole-genome sequencing reads every base, including the rare, high-impact and structural variants an array physically cannot see, with fuller detail on how your body handles medicines. Same areas, same hand-written interpretation, simply more of your DNA in view.

DNA array

Well-studied markers

Whole genome

Every base, rare variants too

Request your consultationArray or whole genome, compared

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.