AI DNA analysis
AI DNA analysis from the raw file you already have.
Upload a compatible 23andMe, AncestryDNA, or MyHeritage raw DNA file and turn selected genetic findings into readable educational reports. GenoSight uses AI for report synthesis, not as a black-box raw-genome dump.
AI boundary
The raw genotype file is not sent to the LLM.
- Educational reports, not medical diagnosis or treatment
- Raw genotype file is not sent to the LLM
- Reports separate stronger evidence from weaker signals
- Clinical decisions still belong with qualified care
How GenoSight uses AI
The useful part is not asking a chatbot to read a giant raw file. The useful part is structured analysis first, then evidence-aware synthesis.
Parse the raw file
GenoSight reads compatible 23andMe, AncestryDNA, and MyHeritage raw genotype files into structured variant rows.
Match curated engines
The analysis layer checks curated lifestyle SNPs, PharmGKB drug-gene context, ClinVar-style disease-variant context, and GWAS-backed signals where coverage exists.
Synthesize with AI
The AI step sees selected structured findings plus your profile context, then writes a readable educational report with caveats and source notes.
Ask grounded follow-ups
Paid plans include chat grounded in the generated report and findings, so follow-up answers stay tied to the evidence trail.
Keep AI inside a narrow job.
AI can make genetic findings easier to read, but it can also be overconfident if the source material is weak. GenoSight keeps medical boundaries, uncertainty, and missing-data caveats visible throughout the report.
How AI reads your DNA
The five-stage GenoSight pipeline from file parsing to AI synthesis and citation validation.
Raw DNA data privacy
How raw genotype storage, report synthesis, and follow-up chat are separated.
Where insights come from
A guide to the evidence sources used in reports, including ClinVar, PharmGKB, GWAS Catalog, and PubMed.
Common AI-assisted report paths
AI genetic analysis
Use the broader AI genetic analysis page if you are comparing AI report workflows before choosing a report path.
Open pathDNA health report
A broad first stop for educational genetic-health context from a compatible consumer raw DNA file.
Open pathMethylation analysis
Review MTHFR, COMT, folate, B-vitamin, and Detox & Methylation context without claiming to measure methylation levels.
Open pathCaffeine sensitivity
Frame ADORA2A sensitivity and CYP1A2 metabolism markers alongside real caffeine habits and cautious boundaries.
Open pathAPOE context
Handle APOE marker context carefully, with counseling-aware limits and no standalone disease-risk verdict.
Open pathPharmacogenomics context
Use drug-gene findings as discussion context only, not dosing, prescribing, or clinical PGx-test replacement.
Open pathSample report
Preview the report structure, source trail, and follow-up flow before uploading a sensitive raw DNA file.
Open pathAI DNA analysis questions
What does AI DNA analysis mean in GenoSight?
It means the raw genotype file is first parsed into structured findings, then an AI model synthesizes selected findings with your profile context into an educational report. The raw file itself is not sent to the LLM.
Can AI analyze my 23andMe or AncestryDNA raw data?
GenoSight can analyze compatible 23andMe, AncestryDNA, and MyHeritage raw genotype files. Coverage varies by provider and chip version, so the report states when data is missing or uncertain.
Is AI DNA analysis a medical test?
No. GenoSight is educational only. It does not diagnose disease, predict outcomes, prescribe supplements or medication, or replace a clinician or genetic counselor.
Which report should I run first?
Use the report picker or start with the broad DNA Health report if you are not sure. New accounts receive 250 free credits, and the first lightweight report can usually be tried without a card.