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$5/month No extra fees No upgrade tiers

DNA Lab Understand your file.

Upload a raw DNA file and get clear research reports: health clues, heritage signals, lineage clues, interactive country map, DNA sound, PDF export, and an optional DNA Agent follow-up lane.

Research support only. Health output is not diagnosis or treatment advice. Heritage output is DNA similarity context, not culture, nationality, religion, tribe, or legal identity.

MapExplore regions
PDFDownload report
AgentAsk follow-ups

Before you upload

Know what fits, what moves, and what the results mean.

Genetic data is sensitive. DNA Lab asks for an explicit upload choice, keeps report generation separate from AI follow-up, and labels results that are experimental, withheld, or limited by the file.

File compatibility

Plain text, up to 30 MB

Use an uncompressed .txt, .csv, .tsv, .vcf, .dna, .genome, or .raw genotype export. Provider-style tables from 23andMe, AncestryDNA, and MyHeritage are supported when they contain SNP/position/genotype rows. Plain-text VCF needs genotype sample calls.

ZIP and GZIP files are not accepted. Extract the provider download on your device, then choose the underlying text file. Renaming an archive does not convert it.

Privacy flow

You choose each sensitive step

  1. Your selected file is sent to ZeroThink for the report after you confirm you have authority to use it.
  2. The raw file is added to your private DNA library only if you select the save option; saved DNA is excluded from general library search and normal AI context.
  3. DNA Agent is optional and has a separate consent. It receives a minimised derived summary for that request, not raw genotype rows or exact genotype identifiers, and that sensitive exchange is not added to normal chat history.

Server handling, suppliers, retention, user rights, and privacy contacts are explained in the ZeroThink Privacy Policy.

Method boundaries

Observed calls, not a clinical test

  • Health matching uses directly observed, quality-eligible calls. A missing or no-call marker is not treated as a negative result, and unobserved variants are not imputed.
  • Genome build, strand/orientation, file coverage, chip version, and reference-allele agreement can change what is matchable. Interpretation is withheld when those checks are not strong enough.
  • Heritage results are experimental similarity signals against available reference panels—not calibrated genealogical percentages or proof of identity.
  • Lineage, ancient-match, theory, and sound lanes are exploratory. They are shown separately from stronger evidence.

Reports record the analysis-engine and source-pack status available at run time. Reference releases and methods evolve, so a later rerun may differ.

One upload, clear cards

Built for people, not genetics experts.

Health Research

Educational marker cards that distinguish directly observed matches, unavailable evidence, and withheld interpretation. They are research leads—not screening, diagnosis, or a negative test.

Heritage Signals

Plain country and region signals with confidence, plus a deeper evidence ledger for users who want to inspect the reasoning.

Lineage Clues

A starter lineage lane for surnames, places, GEDCOM trees, famous-person hypotheses, and what evidence is still missing.

Living Map

Interactive world map bubbles for the user’s strongest DNA similarity signals, built for mobile and desktop exploration.

DNA Sound

An experimental ambience mode that turns marker patterns into a listenable DNA sound profile.

PDF + Agent

Download your report, then optionally ask DNA Agent to explain a minimised summary in normal language. The Agent step is separately disclosed and consented.

Simple price

$5

per month

No extra fees. No separate DNA upgrade ladder. No hidden premium report unlocks for the core DNA Lab experience.

Start DNA Lab

What the user gets

Raw DNA upload

Uncompressed TXT, CSV, TSV, VCF, DNA, GENOME, or RAW genotype files, up to 30 MB each.

Clear summary first

Plain-English cards before deeper evidence notes.

Interactive map

Tap regions, zoom, and explore the strongest signals visually.

Private library option

Save a private copy only when you choose; sensitive DNA stays outside general library search and AI context.

Illustrative report preview

Read the confidence before the conclusion.

Every useful DNA result needs context. The report starts with file quality and interpretation readiness, then separates observed evidence from missing coverage and experimental outputs. This preview shows the structure—not a real person’s data or a promised result.

Create your report
Illustrative DNA report showing file checks, an observed research marker, an unavailable marker, and an experimental heritage signal.

DNA report preview

Evidence first

Illustrative only
File checksBuild · orientation · QC

The report explains whether evidence is ready to interpret or why it was withheld.

ObservedAllele-aware research match

A directly observed call can link to its evidence source and review status.

UnavailableNot measured is not negative

No-call, absent, or incompatible evidence is labelled instead of turned into reassurance.

ExperimentalReference-panel similarity

Heritage and exploratory lanes stay visibly separate from health-evidence cards.

Honest boundary

Bold results, clearly labelled.

DNA Lab can be useful and exciting without pretending. It can show research leads, country/region similarity signals, health-research cards, and lineage clues, while clearly separating evidence from identity, culture, diagnosis, or proof.

Yes: clear research reports, DNA similarity signals, map exploration, and follow-up explanations.

No: medical diagnosis, treatment advice, legal identity claims, tribe/citizenship proof, or royal proof from raw DNA alone.

Ready to try it?

Open DNA Lab inside ZeroThink, upload your raw file, and run the full report. The core DNA product is $5/month, with no extra fees or upgrade tiers.

By using DNA Lab, you agree to the ZeroThink Terms and acknowledge the ZeroThink Privacy Policy.