Your data. Seen clearly.

Good data should come with an honest translation.

My wife lives with chronic illness. I've watched her be dismissed by providers, talked over, told her symptoms aren't that bad. I've seen the gap between what science actually knows and what makes it into a doctor's office.

People need someone to sit down, look at the actual published studies, and say: here's what the research found, here's how strong the evidence is, and here are the questions to bring to your doctor.

I'm a bioinformatics researcher. I build open-source tools for phylogenetics and genomics. I'm not a geneticist or a clinician. But I know how to find published research, evaluate the evidence, and present it honestly. That's what Elpis does. Nothing more, nothing less.

Four reports. Thirty variants. All free.

Each report covers one area of health genetics, drawn from peer-reviewed research and read from the 23andMe or AncestryDNA file you already have.

What we do differently.

Three commitments, each of which costs us something. That's how you can tell they're real.

This is paid for by our services work.

Elpis Biosciences has two divisions. The free parser is one. The other is Elpis Research — custom, reproducible bioinformatics pipelines for labs, startups, and research groups, spanning metagenomics through protein structure prediction.

Services engagements are what fund the consumer reports. No investors, no advertising, and no path where genetic data becomes an asset on a balance sheet. If you hire us, you're the reason someone else reads their own genome honestly, for nothing.