Sequence once.
Know forever.
One saliva kit. One sequencing run. Every AuraGen report — now and as science advances — powered by the same DNA.
RUOResearch Use Only · Not FDA-cleared or approved
- ✓30x average exome coverage · Illumina short-read sequencing
- ✓Captures ~85% of known disease-causing variants
- ✓Powers all 3 included reports + all 4 exclusive add-ons
- ✓Intelliseq iFlow™ HIPAA-compliant pipeline (~4 hr processing)
- ✓~4 week turnaround from lab receipt · secure portal access
- ✓Lifetime data storage · raw VCF download available
- ✓HIPAA-compliant · you own your data at all times
⚠ Research Use Only · Not FDA cleared
- ✓30x whole-genome coverage · every base pair, coding & non-coding
- ✓Structural variants, CNVs, and mitochondrial genome included
- ✓Powers all current + all future AuraGen panels
- ✓Intelliseq iFlow™ HIPAA-compliant pipeline (~4 hr processing)
- ✓~4 week turnaround · raw FASTQ download available
- ✓Required for Longevity & Biological Age panel (coming 2026)
- ✓All WES features included · same turnaround time
⚠ Research Use Only · Not FDA cleared
The PGS Catalog adds validated models monthly. Your DNA doesn't change — but what we know about it does. Refresh re-runs your data against new models annually and notifies you of clinically meaningful new findings.
WES vs WGS — side by side.
The pipeline behind every AuraGen report
AuraGen is built on Intelliseq's iFlow™ engine — a cloud-based, clinically-validated NGS analysis platform that translates raw DNA sequences into complete reports in approximately 4 hours. Already deployed with DNAnexus Precision Health Cloud, reference labs, and DTC companies globally. Intelliseq secured €4.5M in funding (March 2025) to expand US operations.
Common questions.
If your goal is health insights from current AuraGen reports, WES captures everything you need at a lower price. If you want complete genomic coverage, access to future panels requiring non-coding data, or want to download your raw sequencing data, WGS is the better long-term investment.
Once your sample arrives at our lab partner, sequencing takes approximately 3–4 weeks. Bioinformatics processing via Intelliseq iFlow™ adds approximately 4 hours. Your three included reports are delivered simultaneously to your secure portal.
After your sequencing is complete, every add-on report (GLP-1 Response, Cardiovascular Chain, Women's Health, Skin + Cancer) is unlocked instantly on purchase — no new kit, no new sample. Each one is a new query against your existing variant data.
You do. Always. Your variant file is stored on HIPAA-compliant infrastructure and you can download it or request permanent deletion at any time. AuraGen never sells or shares identifiable genomic data with third parties. See our Data & Privacy page for full details.
DNA upload functionality from third-party providers is on our roadmap. Currently, reports require sequencing through an AuraGen kit to ensure sufficient variant coverage for our PRS and PGx panels.
All AuraGen kits and reports are for Research Use Only (RUO) and are not FDA-cleared, FDA-approved, or CE-IVD certified. Polygenic risk scores and pharmacogenomic findings are not diagnostic tests. Results reflect statistical associations from published peer-reviewed GWAS studies and do not predict with certainty whether any condition will develop. Always consult a licensed healthcare provider before making any medical, pharmacological, or lifestyle decision based on these findings. © 2026 AuraGen Wellness · auragenwellness.com