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Helixir Genomicshelixirgenomics

About

A small practice, for the life ahead.

Helixir Genomics is a one-person practice. Your DNA holds clues worth understanding, and reading them well is the work of a scientist, not an algorithm. So one scientist reads yours, personally.

The scientist

Adriano De Marino, founder and precision medicine analyst, Helixir Genomics

Helixir Genomics · Founder

Adriano De Marino, PhD.

Adriano De Marino, PhD.

Adriano is a precision medicine analyst with a PhD. He has spent years inside the largest commercial genomics platforms, reading DNA at scale. That work convinced him of a simple thing: the most useful reading is still done one person at a time, by a scientist who knows the science.

So he reads each genome himself. He turns it into a few clear choices that add up over a lifetime, writes them in plain language, and signs his name to the result.

Read more about Adriano →

Discipline

Precision medicine

Method

Read by a scientist, not an algorithm

Scope

One person at a time

Standards

Four rules your analysis is held to.

Evidence

Every finding is checked against ClinVar, the public database of gene–health links, and the current peer-reviewed research. Nothing comes from a black-box model.

Restraint

When the science is uncertain, we say so plainly. We do not claim more than the data can support.

Privacy

Your data is yours. Never sold, never shared for advertising or research, never used to train models. Encrypted on our servers and while it travels.

Independence

We earn nothing from any supplement brand, lab, or drug. So the advice you get is the advice we believe, with no one paying for the answer.

How deep you read

For the deepest read, the whole genome.

Depth is yours to choose. An array reads the well-studied, pre-selected markers across your DNA. Whole-genome sequencing reads every base, reaching the rare, high-impact and structural variants an array physically cannot see, plus fuller detail on how you respond to medication. The areas are the same, and the hand-written interpretation is the same; the whole genome simply gives the scientist more of your DNA to read.

One at a time

One genome, one scientist, one plan.

We take on only a few people at a time, on purpose. That keeps the work careful, the attention personal, and your analysis truly your own.