Every product, in depth

Six surfaces, one genome.

Three one-time reports and three Studio subscriptions. Each one built around a single principle: read the same raw DNA file with scientific rigor, give you back something interpretable, and respect your data the entire way through. This page is the deep dive — what each product is, how it works, and why it's worth the money.

3 one-time reports 3 studio subscriptions 1 raw DNA upload 1-day free trial on subscriptions
/ 01 · One-time report

Modern Ancestry & Haplogroups

Continental and regional ancestry mapped against modern reference populations, paired with paternal and maternal haplogroup lineage. The flagship deliverable.

One-time purchase
€21.20/ lifetime access
Includes Y-DNA + mtDNA bundled Buy now View detailed page
Modern Ancestry report sample — top section showing the self-portrait, continental breakdown and named regional populations

What it actually is

A structured, interactive on-platform report that lives on your dashboard and tells you which modern populations your DNA sits closest to — at the continental level, the regional level, and where the data supports it, the sub-regional level. Anglo-Italian-Iberian-French is not enough; we resolve down to "Northern Italian alpine valleys" or "Lebanese Maronite peoples of Zgharta" when the signal is there.

Bundled with the report: your Y-DNA haplogroup (paternal direct line) and mtDNA haplogroup (maternal direct line) with terminal-SNP-level depth where your file's coverage allows.

How it works

  1. 01Upload your raw DNA file. AncestryDNA, 23andMe, MyHeritage, FTDNA, LivingDNA, Sequencing.com — we handle them all.
  2. 02We compute NexoGENO proprietary ancestry coordinates from your genotype, then run NexoGENO's in-house ancestry-fitting engine against curated modern reference panels.
  3. 03Y-chromosome and mitochondrial haplogroups are called in parallel from the same upload, with confidence tiers.
  4. 04You receive the report on your dashboard plus a high-resolution image export, with every population labelled and sourced.

What you get

  • Continental breakdown (e.g. South European 62.4%, Levantine 18.1%, …) with confidence intervals
  • Regional breakdown with sub-region resolution where the data supports it
  • 1,200+ modern reference populations across Europe, MENA, South / Central / East Asia, the Americas, Africa, Oceania
  • Y-DNA haplogroup down to terminal SNP (paternal lineage)
  • mtDNA haplogroup down to terminal SNP (maternal lineage)
  • Per-region narrative with historical context, not just a pie chart
  • Lifetime access — view it on your dashboard whenever you want

Why it's worth the money

Sub-regional resolution

The big consumer tests stop at "Italian." Ours resolves down to specific populations and valleys.

Bundled lineage

Y-DNA + mtDNA included at no extra cost — separately, those would each be a paid add-on elsewhere.

Privacy-by-default

Your raw file isn't sold, syndicated, or used to train anyone's model. You stay in control of deletion.

0reference populations
0typical turnaround
Lifetimelifetime dashboard access
/ 02 · One-time report

Ancient DNA Ancestry

Connections to named ancient civilizations — Bronze Age Anatolia, Roman Latium, Bohemian Gauls, Pannonian Iron Age — drawn from archaeogenetic samples, not modern proxies.

One-time purchase
€10.60/ lifetime access
Reads from the same upload Buy now View detailed page
Ancient DNA Ancestry report sample — top section showing named ancient civilizations: Siculi, Iberian Tartessian, Etruscan, Ausoni, Roman Hispania, Gaul, Roman Imperial, Roman Latini and more

What it actually is

A separate report — usable on its own, but most powerful paired with the Modern report — that compares your genome against the growing public corpus of ancient DNA samples recovered from archaeological digs. Where Modern tells you "you look like a Lebanese Maronite," Ancient tells you "you carry signal from Roman Latium / Imperial Era and Pannonian Gauls / Iron Age."

Useful for users who want to feel the depth of their lineage in historical terms rather than just modern political ones.

How it works

  1. 01Same raw upload as Modern. If you've already paid for Modern, the Ancient report reads from the file already on your account.
  2. 02Modelled against archaeogenetic samples from peer-reviewed publications: Reich Lab releases, Allentoft, Mathieson, Lazaridis and others, deduplicated and curated.
  3. 03Best-fit ancient population mixtures are computed and ranked by genetic distance, with named civilization labels and date ranges.
  4. 04Each ancient population gets historical context — who they were, when they lived, where they were dug up, what we know.

What you get

  • Best-fit ancient mixture model with named civilizations and time ranges
  • 3,820+ archaeogenetic samples drawn from published archaeological excavations
  • Historical context per population — where the samples came from, what era, what culture
  • Ancient lineage tags (Bronze Age, Iron Age, Late Antiquity, Imperial Era, etc.)
  • Bohemian Gauls, Vesigneul, Pannonian Gauls, Greco-Roman Emporiae, Hispania, Roman Latium and many more
  • Comparison to your Modern result so you see the deep-time origin of each modern slice
  • Lifetime access — same as Modern

Why it's worth the money

Real archaeogenetic data

Not modern populations relabelled "ancient." Actual samples recovered from named dig sites.

Time-depth context

Eras, dates, civilisations with names, not just abstract genetic clusters.

Pairs with Modern

The deep-time companion that explains where your modern populations actually came from.

0ancient samples
0time depth covered
Same fileno re-upload needed
/ 03 · One-time report

Health & Traits Report

Selected health predispositions, traits, and genetic markers, presented with context — not headlines. The lightweight intro to your genome's health-relevant signal.

One-time purchase
€6.36/ lifetime access
Educational, not diagnostic Buy now View detailed page
HEALTH & TRAITS Selected genetic markers PHARMACO TRAITS CARRIER Caffeine metabolism (CYP1A2) Slow metaboliser. Caffeine clears slower than average. VARIANT EVIDENCE B Lactose persistence (LCT) European-type variant present. Adult lactose tolerance likely. PHENOTYPE APOE risk variants (Alzheimer's) ε3/ε3 genotype. Population-baseline risk. Educational only. EDUCATION 42 MARKERS · CONTEXT & CONFIDENCE NOTED

What it actually is

A curated set of health-relevant genetic markers — pharmacogenetic variants, classic carrier markers, common traits — explained in plain language with sources, confidence, and population context. The lightweight introduction. If you want pharmacogenetics pipelines, polygenic risk scores and modular health reports, that's the Health Studio subscription further down this page.

How it works

  1. 01Same upload as the ancestry reports. No second swab, no second file.
  2. 02We check coverage for each marker — if your file doesn't include the relevant SNP, we say so explicitly instead of inventing a result.
  3. 03Each marker is annotated with what's known, the strength of evidence, and the appropriate caveat.
  4. 04You receive a structured report on your dashboard with searchable cards, not a wall of acronyms.

What you get

  • Selected health-relevant variants (pharmacogenetic, carrier, common traits)
  • Plain-language explanation per marker with source citations
  • Coverage notes — when your raw file doesn't have the SNP, we tell you
  • Population context: how common this variant is in your ancestry
  • Clear separation between trait-level (height, caffeine) and risk-level (clinically meaningful) markers
  • Educational-only framing — never diagnostic, never alarmist

Why it's worth the money

Calibrated, not alarmist

Population baselines explained, not "you carry the gene for X" headlines.

Honest about coverage

We tell you what your file does and does not contain. Missing SNPs are flagged, not silently filled.

Cheap entry point

€6.36 is a coffee. If you want the full pharmacogenetics + PRS pipeline, upgrade to Health Studio.

/ 04 · Subscription · Most popular

NexoGENO Studio

Not a DNA tool. A complete genetics workspace in your browser. Sixteen connected modules that take you from a raw DNA upload all the way through interpretation, comparison, visualization, editing, simulation, and export — without leaving the environment.

Subscription · most popular
€14.99/ month
1-day free trial · cancel anytime Start free trial View detailed page
NexoGENO Studio homepage workspace — the orientation layer of the platform

What it actually is

NexoGENO Studio is structured more like a professional laboratory dashboard than a consumer DNA result page. Instead of giving you one ancestry estimate and stopping there, it gives you a toolkit for testing, refining, stress-checking, comparing, and visualising genetic results from multiple angles. DNA data is worked on, not just viewed.

Most people who do serious raw-DNA work today have to bounce between separate tools — one to convert files, another to generate coordinates, another to model ancestry, another to make maps, another to compare kits, another to inspect matches. Studio collapses that whole chain into one continuous web environment.

The four core workflows

  1. 01Raw DNA → ancestry model. Upload your file. Generate G25 coordinates. Send them straight into TARGET. Load source populations. Run SINGLE for a model, or MODEL FINDER to compare candidate models. Validate with DISTANCE, PCA MAP, HEATMAP, or TARGET COMPARER.
  2. 02Raw DNA → chromosome-level ancestry. Upload into CHROMOSOME PAINTER. The platform generates full-file plus chromosome-specific coordinates, models them against your source set, and paints ancestry across chromosomes 1 to 22 — with high-resolution image export.
  3. 03Kit matching + segment interpretation. Upload a base kit and one or more target kits into MATCHES. Compute shared segments, cM totals, relationship-style metrics, chromosome-level overlap. The Chromosome Match Painter overlays segments with ethnicity blocks from CHROMOSOME PAINTER.
  4. 04Coordinate editing & simulation. Don't just accept results — modify them. Remove components, build hypothetical coordinates, rebalance models interactively, run automated decomposition. A sandbox for hypothesis testing, teaching, and scenario work.

What you can do inside the Studio

Sixteen connected modules. Workflows that chain together. New tools shipping every month. Subscribe to discover the endless things you can do with NexoGENO Studio.

View the full module breakdown →

Why it's worth the money

Replaces a desktop toolchain

nMonte + Vahaduo + spreadsheets + image editors + segment tools → one connected, browser-only workspace. No installs, no version drift, no jumping between programs.

Continuously updated

New populations, new ancient sample releases, new methods, new modules — they all land in your account automatically. Your subscription pays for the workshop staying current with the science.

Exportable everything

Image, CSV, JSON outputs from every module. Your work leaves the platform with you — including high-resolution chromosome paintings, PCA renders, and heatmap exports.

16integrated modules
0reference populations
5+ vendorsauto-detected on upload
/ 05 · Subscription

NexoGENO Haplogroup Studio

A dedicated Y-DNA and mtDNA lineage analysis platform that turns common consumer files, VCF, FASTA, and other genotype formats into clear haplogroup results — backed by real marker evidence rather than a black-box label.

Subscription
€9.99/ month
1-day free trial · cancel anytime Start free trial View detailed page
NexoGENO Haplogroup Studio — real results page with Y-DNA and mtDNA call output

What it actually is

A focused workspace for haplogroup work specifically. Where the one-time Modern report bundles a single Y + mtDNA call from your one file, the Haplogroup Studio is the workshop: upload many files in many formats, get official haplogroup calls with marker evidence, see the lineage path, see deep-clade hints, see conflict warnings when two methods disagree.

How it works

  1. 01Upload from any source: 23andMe / AncestryDNA / FTDNA / MyHeritage genotype files, FASTA mtDNA sequences, VCF whole-genome calls, custom marker exports.
  2. 02Multi-method calling runs in parallel: traditional ISOGG-tree marker checks, phylogenetic placement, FASTA-vs-rCRS difference scoring.
  3. 03You see the actual evidence — which SNPs were called, which weren't, which support the call, which contradict it.
  4. 04Confidence tiers, deep-clade hints, conflict warnings separate strong conclusions from speculation.

What you get

  • Y-DNA + mtDNA from consumer files, VCF, FASTA, and other genotype formats
  • Official haplogroup calls with the supporting marker evidence visible
  • Lineage path context plus confidence tiers
  • Deep-clade hints and conflict warnings when signals disagree
  • Multi-method calling separates strong conclusions from speculation
  • Process unlimited files inside the subscription window
Haplogroup Studio HD share card — the real shareable Y-DNA + mtDNA result output the platform exports for clients

Why it's worth the money

Evidence, not labels

Every haplogroup call exposes its marker evidence so you can verify the call yourself.

Many file formats

VCF, FASTA, every consumer vendor — one workspace handles them all.

Conflict-aware

When two methods disagree, we surface the disagreement instead of hiding it. Genealogy needs that.

/ 06 · Premium subscription

NexoGENO Health Studio

A web-based DNA health analysis platform that turns raw genetic data into a structured, easy-to-read health report. Modular dashboard cards, plain-language explanations, and export-ready outputs — in one professional interface.

Premium subscription
€49.99/ month
For serious health-context research Subscribe View detailed page
HEALTH STUDIO Modular health report cards PHARMACOGENETICS 28 drug genes CYP2D6, CYP2C19, … POLYGENIC RISK 12 PRS panels Cardio, metabolic, … CARRIER SCREENING Classic panel CFTR, HEXA, BRCA, … MONOGENIC FINDINGS ACMG-aligned Reportable variants CONFIDENCE & COVERAGE Every card carries an evidence tier. Plain-language explanations + searchable tables.

What it actually is

The professional health-side workspace. Where the €6.36 Health & Traits report is the lightweight intro, Health Studio is what serious researchers, careful users, and second-opinion seekers actually need: pharmacogenetics, polygenic risk scores, carrier screening, monogenic findings, all modular, all with confidence and coverage notes, all explained in plain language, all exportable.

How it works

  1. 01Same upload as everything else. Standard consumer DNA files — no extra test required.
  2. 02Each module runs independently: pharmacogenetics, PRS panels, carrier screening, monogenic findings, traits.
  3. 03Each card shows its confidence tier and coverage — what was checked, what wasn't, how strong the evidence is.
  4. 04Export the whole report as a high-resolution image set or as JSON for downstream tooling. Continuously updated as panels grow.

What you get

  • Polygenic risk scores plus phenotype-style traits
  • Pharmacogenetics, classic carrier screening, monogenic findings
  • Modular dashboard cards with confidence and coverage guidance
  • Plain-language explanations and searchable tables
  • Top-insights view + export-ready outputs (high-resolution images / JSON)
  • Selected health-related trend reports

Why it's worth the money

Modular cards

Open only the surfaces you care about today. Each card is independent and self-contained.

Confidence-first

Every card carries an evidence tier and coverage note. No silent assumptions, no panic-headlines.

Export-ready

high-resolution image export for your records, JSON for downstream tooling. Your data leaves the platform with you.

Side by side

Which one is right for you?

One-time reports give you a deliverable. Studios give you a workspace. Mix freely.

Modern Ancestry Ancient DNA Health & Traits NexoGENO Studio Haplogroup Studio Health Studio
Format One-time report One-time report One-time report Subscription Subscription Premium subscription
Price €21.20 €10.60 €6.36 €14.99 / mo €9.99 / mo €49.99 / mo
Modern populations — — — —
Ancient samples — — — —
Y-DNA + mtDNA Bundled — — Bundled Deep tooling —
Health markers — — Selected — — Full pipeline
Workspace tooling — — — Full Haplogroup-only Health-only
Continuously updated — — —
Common questions

Before you buy.

Do I need a new DNA test, or can I bring my existing file?
You bring your existing raw DNA file. NexoGENO accepts files from AncestryDNA, 23andMe, MyHeritage, FTDNA, LivingDNA, Sequencing.com, plus VCF / FASTA where appropriate. There is no swabbing kit on our side — we are an interpretation platform.
Can I buy reports separately, or do I need a Studio subscription?
The three reports (Modern, Ancient, Health & Traits) are one-time purchases — you pay once, you keep them. The three Studios are monthly subscriptions for the deeper interactive workspace. Most people start with one or two reports and only move to a Studio if they want to keep working with their data.
What happens to my raw DNA file?
Your file stays bound to your account. We do not sell, syndicate, or use it to train any model. You can delete it from the dashboard at any time — deletion is real, not soft-archived.
How long does a report take to generate?
Typical turnaround for the one-time reports is around 24 hours. Studio results are interactive: you ask, the workspace computes on the spot.
Is the Health Studio a replacement for medical advice?
No. Health Studio is an interpretation and research workspace. It surfaces pharmacogenetic variants, polygenic risk scores, carrier panels and monogenic findings with confidence tiers and plain-language explanations — but every output explicitly carries the educational, non-diagnostic framing. Talk to a clinician for medical decisions.
What if my file doesn't cover a specific marker?
We tell you. Coverage is checked per-marker and surfaced explicitly — if your raw file does not contain the SNP needed for a given call, the result is marked as "not covered" rather than silently filled. Honest reads are part of the product.
Can I cancel a Studio subscription?
Any time, from your dashboard. The first day is free on the trial-eligible tiers. Cancellation is immediate; no email gauntlet.
One genome, six surfaces

Start with the file you already have.

Upload your raw DNA, pick the products that fit, get back something interpretable. The reports last forever; the Studios run as long as you need them.

Upload your RAW data View report samples