The difference
They read
0.02%
Genotyping chip
A saliva-based chip reads a tiny sliver of your DNA. Limited coverage. No structural variants. No follow-up. A snapshot from 2007 technology.
We sequence
100%
Full-genome truth
PacBio HiFi long-read whole genome sequencing from clinical-grade blood. Every base pair. Every structural variant. Paired with ongoing personalized monitoring.
3.2B
base pairs
30×
coverage depth
100%
of your genome
The science
Built on the most accurate
sequencing technology available
99.9%
Single-molecule read accuracy
PacBio HiFi consensus
<1%
CYP2D6 error rate
vs 10–15% with short-read
100%
Structural variants detected
Expansions · SVs · CNVs
Blood is a feature, not a compromise.
Clinical-grade capillary blood delivers measurably better data quality than saliva. Lower bacterial contamination. Better structural variant detection. More consistent coverage. Every competitor uses saliva because it's cheaper. We use blood because the data is better.
How it works
Four steps to your complete picture
01
Order your kit
Delivered to your door in 2–3 days. Everything you need in one box.
02
Collect at home
Painless Tasso+ blood collection from your upper arm. No needles. No lab visit. 5 minutes.
03
We sequence everything
PacBio HiFi long-read whole genome sequencing. 100% of your DNA at 30× depth.
04
Get your Axiom Audit
Genome report, baseline blood panel, pharmacogenomics, and personalized monitoring plan.
What you get
Everything in one collection
Two painless Tasso+ devices. One box. Your complete genomic and biomarker profile.
Pharmacogenomics
Know which drugs work for YOUR body. Long-read resolves CYP2D6 with near-zero error — no more guessing.
Structural Variants
Catch what short-read misses. Repeat expansions, large deletions, complex rearrangements — all resolved.
Carrier Screening
Phased results show which parent each variant came from. Distinguish cis from trans for accurate risk assessment.
Raw Data Access
FASTQ, BAM, VCF — you own your genome. Download it. Delete it. It's yours. No lock-in.
Blood Biomarkers
Baseline panel from the same collection. Glucose, HbA1c, lipids, CRP, vitamin D — and more.
Axiom Age
Track your biological age over time with methylation clock testing. Annual pace-of-aging trend.
Pricing
Choose your depth
Every tier includes full long-read whole genome sequencing.
Genome Audit
one-time
Join Waitlist- PacBio HiFi 30× long-read WGS
- 2× Tasso+ at-home blood collection
- Axiom Audit Report
- Baseline blood panel
- Raw data access (FASTQ/BAM/VCF)
- Secure delivery + deletion option
Executive
one-time
Join Waitlist- Everything in Genome Audit
- 60–90 min genome walkthrough
- Priority turnaround (2 weeks)
- "Next Steps" module for your doctor
- Personalized monthly monitoring plan
- Dedicated support
Axiom Black
one-time
Join Waitlist- Everything in Executive
- 24-month reanalysis membership
- 12 monthly genome-guided blood panels
- 1–2× annual Axiom Age testing
- Priority everything
- Early access to new features
Monthly monitoring
Sequenced once.
Monitored forever.
Every month, we mail a painless Tasso+ kit. Collect a blood sample, send it back. We run a personalized panel of 8–12 biomarkers — informed by your genome, not a generic menu.
We don't test everything. We test what your DNA says matters.
MTHFR C677T
Homocysteine, Folate, B12
Variant impairs folate metabolism
APOE ε4 carrier
ApoB, hs-CRP, Lp(a), Lipid Panel
Elevated cardiovascular + neurological risk
CYP2D6 poor metabolizer
Drug metabolite levels
Standard doses may be too high or ineffective
FAQ
Common questions
23andMe reads 0.02% of your DNA using a genotyping chip and saliva. We sequence 100% of your genome using PacBio HiFi long-read technology from clinical-grade blood — and provide ongoing monthly blood monitoring guided by your genomic data. No other company offers this combination.
Axiom provides educational genomic data and wellness-oriented blood biomarker panels. We are not a diagnostic service and do not provide medical advice. Your results are designed to be shared with your healthcare provider for clinical interpretation.
We use the Tasso+ device — an FDA-cleared, painless capillary blood collection device that attaches to your upper arm. No needles, no lab visit. It collects approximately 500 µL of blood in about 5 minutes with a 93% first-attempt success rate.
You own your data. We deliver raw genome files (FASTQ, BAM, VCF) via secure download. You can request full deletion at any time — we destroy all samples and data within 30 days. No exceptions.
We're currently in early access. Join the waitlist to be first in line. Early members receive priority access and founder pricing.
Be first to know.
Join the waitlist for early access and founder pricing.
No spam. Just science.