GenomicsCPU5 credits

Personal Genomics Lab

Upload 23andMe or AncestryDNA data for trait analysis, pharmacogenomics, and ancestry

A privacy-first personal genomics platform. Upload your raw DNA data — it's parsed entirely in your browser and never sent to our servers. Get trait analysis across 400+ clinically relevant SNPs, pharmacogenomics reports for drug-gene interactions, ancestry markers, and Neanderthal variant detection.

$0.05
per API call
5
credits per call
POST /v1/personal-genomics/upload
API endpoint

Features

Privacy-first: raw data parsed in browser, never uploaded
400+ curated SNP annotations from ClinVar, PharmGKB, GWAS Catalog
Trait analysis: eye color, hair, taste, muscle type, and more
Pharmacogenomics: CYP2D6, CYP2C19, VKORC1, DPYD drug interactions
Health risk markers: APOE, MTHFR, BRCA tag SNPs, diabetes loci
Neanderthal variant detection (18 introgressed markers)
Ancestry-informative markers with population frequencies
AI-powered genome chat assistant

Quick Start

SciRouter Annotation Engine — Python Examplepython
import requests

# Upload derived results (after client-side parsing)
response = requests.post(
    "https://api.scirouter.ai/v1/personal-genomics/upload",
    headers={"Authorization": "Bearer sk-sci-your-key"},
    json={
        "filename": "my_23andme.txt",
        "chip_version": "v5",
        "snp_count": 640000,
        "snp_count_valid": 635000,
        "call_rate": 0.992,
        "trait_results": [],
        "pharmgx_results": []
    }
)
print(response.json()["data"]["id"])

Use Cases

1

Upload 23andMe v3/v4/v5 raw data files for instant analysis

2

Check drug-gene interactions before starting new medications

3

Explore trait genetics — eye color, caffeine metabolism, lactose tolerance

4

Review health risk variants with confidence-rated evidence

5

Match your variants against published research via Literature Radar

Start Using Personal Genomics Lab

500 free credits every month. No credit card required.