Your Complete Genome
Sequence all 3 billion base pairs of your DNA to uncover hereditary disease risk, pharmacogenomic drug responses, carrier status, and actionable genetic insights — then let a physician scientist integrate that data into your complete health strategy.
Powered by Veritas Intercontinental — whole genome sequencing co-founded with Harvard’s George Church, analyzing 576+ genes across 650+ conditions
Why Whole Genome Sequencing Changes Everything
Consumer DNA tests sample a handful of markers. Whole genome sequencing reads every single letter of your genetic code — giving you and your physician the most complete foundation for preventive health decisions you will ever need.
Complete & Permanent
Your genome is sequenced once and stored for life. As science advances, Veritas reanalyzes your existing data against newly discovered variants — no new sample needed, no additional sequencing cost.
Pharmacogenomics Built In
Know how you metabolize 250+ medications before you take them. Maps directly to Dr. Kilgore’s MedCheck Rx™ tool — turning raw pharmacogenomic data into specific, actionable drug guidance.
Physician-Interpreted
Raw genome data without clinical context is noise. Dr. Kilgore integrates your Veritas results with your bloodwork, epigenetics, and wearables to build a strategy — not just a report.
The Four-Layer Data Integration Framework
Every layer tells a different part of the story. Genomics is Layer 1 — the permanent foundation that every other layer builds upon.
Genetics (DNA) YOU ARE HERE
Your permanent blueprint — all 3 billion base pairs. Veritas’s myGenome sequences your entire genome, revealing hereditary disease risk, pharmacogenomics, carrier status, and 50+ genetic traits. Test once, benefit for life.
Epigenetics
How your genes are expressed right now. TruDiagnostic’s epigenetic clocks reveal your biological age, pace of aging, and organ-specific aging — all modifiable with lifestyle. See Epigenetics →
Biomarkers
Your real-time blood chemistry. Analyzed through 30+ AI-powered calculators on drpaulkilgore.com — from inflammation and lipids to kidney, liver, and metabolic health.
Wearables
Continuous data from Oura, WHOOP, Apple Watch, and CGMs. Heart rate variability, sleep architecture, and glucose responses feed back into the system daily.
All four layers integrated = precision health. Any one alone = a partial picture.
What Whole Genome Sequencing Actually Means
Not all DNA tests are created equal. Consumer kits sample a fraction of your genome. Veritas reads all of it — and expert geneticists interpret what it means for your health.
WGS vs. consumer DNA tests
Consumer services like 23andMe and AncestryDNA use genotyping arrays that read roughly 600,000 to 700,000 positions — less than 0.02% of your genome. Whole genome sequencing (WGS) reads all 3 billion base pairs at 30x coverage, capturing the 99.98% that genotyping misses. This includes rare variants in non-coding regions, structural changes, and pharmacogenomic variants that directly affect how you respond to medications.
| Criteria | Consumer DNA Test | Veritas myGenome (WGS) |
|---|---|---|
| DNA coverage | ~0.02% (genotyping array) | 100% (30x whole genome) ✓ |
| Genes analyzed | Handful of selected SNPs | 576+ genes, 650+ conditions ✓ |
| Pharmacogenomics | Limited or absent | 250+ medications profiled ✓ |
| Reanalysis as science advances | Not available | GenomeLife™ subscription ✓ |
| Genetic counseling included | No | Pre & post-test counseling ✓ |
| Physician interpretation | No | Dr. Kilgore session available ✓ |
What myGenome reveals
A single saliva sample. One sequencing run. Six categories of clinically actionable information that you and your physician can use for the rest of your life:
Clinical Outcomes
576 genes related to 650+ actionable conditions including hereditary cancer, cardiovascular disease, neurological disorders, metabolic conditions, and immune disorders.
Pharmacogenomics
How you metabolize 250+ medications. Includes CYP2D6 (metabolizes 25% of common drugs), CYP3A4, CYP2C19, and more. Feeds directly into MedCheck Rx™.
Carrier Status
225+ autosomal recessive conditions you could pass to children. Essential information for family planning at any age.
Multifactorial Risk
15 conditions where both genetics and environment play a role — risks you can lower through proactive lifestyle modification.
Genetic Traits
50+ individual characteristics related to diet, athletics, longevity, nutrition, metabolism, and more — guided by your unique DNA.
Ancestry
Analysis of DNA variants to establish the genetic origin of your ancestors — going beyond consumer-grade estimates with whole-genome resolution.
WGS vs. FitnessGenes — complementary, not competing
Both are Layer 1 genetics products, but they serve different purposes and pair powerfully together.
Fitness & Nutrition Focus
- 180+ fitness & nutrition traits
- Training optimization
- Macronutrient ratios
- Genotyping (selected SNPs)
Clinical & Preventive Depth
- 650+ disease conditions
- 250+ drug responses
- 225+ carrier conditions
- Whole genome sequencing (30x)
FitnessGenes tells you how to train and eat. Veritas tells you what diseases to screen for, which medications to avoid, and what you could pass to your children. Together, they give you the most complete genetic picture available.
Built on World-Class Science & Infrastructure
Veritas was co-founded by George Church of Harvard Medical School — one of the pioneers of modern genomics. The technology and interpretation standards reflect that pedigree.
Co-founded by Prof. George Church. Disease list selected by a medical team from the Personal Genome Project and Harvard University for prevention-related actionability.
Custom bioinformatics pipeline using Bayesian and heuristic variant callers. Aligned to human reference genome, validated through peer-reviewed research at Clínica Universidad de Navarra.
Reports include all genes recommended by the American College of Medical Genetics and Genomics (ACMG), plus AHA cardiovascular and MODY diabetes panels added in recent updates.
Your genome data is stored and reanalyzed as science advances. New genes, new variants, new clinical guidelines — applied to your existing data without resequencing.
ISO-certified laboratory in Barcelona • Illumina sequencing technology • 30+ countries served • Pre & post-test genetic counseling included
Which Genomic Test Is Right for You?
Answer three quick questions and we’ll recommend the right Veritas test for your health goals — plus send you a personalized guide to understanding whole genome sequencing.
What matters most to you right now?
Have you done genetic testing before?
Which approach fits you best?
We’ve Found Your Match
Enter your name and email to receive your personalized genomic guide plus next steps:
Your information is never sold. Privacy policy →
Your Guide Is On Its Way
Check your inbox in the next 2 minutes (and spam folder just in case). Your personalized guide breaks down exactly what your recommended test covers and how the process works.
Physician-Interpreted • Whole Genome Sequencing • Four-Layer Health Integration
From Saliva to Strategy in 12 Weeks
A simple saliva sample. No blood draw. Veritas’s lab sequences your complete genome, expert geneticists interpret the results, and Dr. Kilgore turns the data into a clinical plan.
Request Your Test
Submit an inquiry below. Dr. Kilgore’s team will confirm your test selection, provide the required physician prescription, and coordinate kit shipment.
Collect at Home
A saliva or blood collection kit ships to your door. Follow the simple instructions and return the sample with the prepaid shipping label. Five minutes, no appointment.
Sequence & Interpret
Veritas’s ISO-certified lab in Barcelona sequences your DNA. Expert geneticists — led by Dr. Luis Izquierdo (CMO) and Dr. Vincenzo Cirigliano (CTO) — interpret every variant.
Receive & Integrate
Your report arrives via secure portal (8–16 weeks depending on test). Add a physician interpretation session to integrate your genomic data into your complete health picture.
Choose Your Level of Genomic Insight
Five tests — from targeted panels to complete genome. All include Veritas’s pre and post-test genetic counseling by physician geneticists. Pricing confirmed after your discovery conversation.
- 30x whole genome sequencing
- 566 genes, 650+ conditions
- 250+ drug responses (PGx)
- 225+ carrier status conditions
- 15 multifactorial disease risks
- 50+ genetic traits & ancestry
- Pre & post-test counseling
- GenomeLife™ reanalysis eligible
- 162 genes analyzed
- Hereditary cancer risk
- Hereditary cardiovascular risk
- ACMG-recommended genes
- Whole-exome sequencing
- Results in ~8 weeks
- Pre & post-test counseling
- ~100 cardiovascular genes
- Cardiomyopathy & arrhythmia
- Sudden cardiac death risk
- AHA guideline-aligned
- Whole-exome sequencing
- Pre & post-test counseling
- 25 genes analyzed
- 129 active ingredients
- Drug metabolism & toxicity
- Guideline-based (CPIC/DPWG)
- Maps to MedCheck Rx™
- Pre & post-test counseling
- Cardiovascular (2M+ variants)
- Type 2 diabetes (600K+ variants)
- Breast cancer (550K+ variants)
- Prostate cancer (650K+ variants)
- CE-IVD certified software
- Risk calculators included
All tests processed through Veritas Intercontinental’s ISO-certified laboratory in Barcelona • Physician prescription required (provided by Dr. Kilgore) • Saliva or blood collection — no lab visit needed
Genomic Data Deserves Clinical Context
Veritas’s physician geneticists provide expert pre and post-test genetic counseling with every test — included at no additional cost. Dr. Kilgore’s interpretation session adds a different layer: integrating your genomic findings with your bloodwork, epigenetics, and wearable data to build a unified clinical strategy across all four health layers.
- 60-minute video session with Dr. Kilgore
- Your Veritas results contextualized clinically
- PGx findings mapped to MedCheck Rx™
- Integration with bloodwork & epigenetics
- Written summary delivered within 48 hours
HSA/FSA eligible • Scheduled via Calendly after booking
