UNDIAGNOSED
When tests say
you're fine but
you're not.
Whether you've been told nothing is wrong, or you're just beginning to wonder. Your instinct is worth investigating.
WHY STANDARD TESTS MISS IT
The difference between a standard test and reading your entire genome.
Standard genetic tests look at a pre-selected set of variants. If your answer is not in that set, it will never be found. Whole Genome Sequencing reads everything.
STANDARD GENETIC TESTING
~700K
pre-selected variants checked
Standard tests (SNP arrays, targeted panels) check a fixed list of known variants. If the variant causing your condition is not on the list, it will not be detected. Most of the genome is never examined.
DANTE WHOLE GENOME SEQUENCING
4.6 to 5M
variants identified across entire genome
WGS reads every base pair in your genome. It identifies 4.6 to 5 million variants, including in regions between genes that standard tests never examine. If the answer is in your DNA, WGS can find it.
"They never added the numbers up until now when they saw the Dante Labs report."
Thomas, Scotland
Queen Elizabeth University Hospital Glasgow, NHS
Thomas spent years with a set of symptoms no specialist had been able to connect into a coherent picture. Despite dozens of consultations and traditional tests, his condition remained a mystery.
It wasn't until he received his Dante Labs Whole Genome report that the underlying genetic cause was finally identified. His NHS clinical team accepted the data and used it directly in his care pathway.
NHS teams accept Dante data
THE GAP
What standard testing misses.
Standard panels test pre-selected variants in a limited number of genes. Whole Genome Sequencing examines all genes, including the regulatory regions between them where many disease-causing variants reside.
Intronic and intergenic regions
The vast majority of your genome sits between genes. Standard tests skip these regions entirely. WGS reads them, and many clinically significant variants are found here.
Structural variants and CNVs
Deletions, duplications, and rearrangements of large DNA segments are invisible to standard panels. WGS detects structural changes that can explain conditions no other test has identified.
Novel and rare variants
If your variant has never been catalogued, a panel test will never find it. WGS captures every variant in your genome, including those that are unique to you or your family.
CLIA Certified
ISO 15189
NHS-Accepted
99.98% Accuracy
WHAT YOU RECEIVE
Everything your physician needs. And a tool to help you understand it.
200+ clinical reports, physician-ready
Organized by clinical category: hereditary risk, pharmacogenomics, carrier status, disease predisposition, and more. Formatted for direct use by your healthcare provider.
Genome Manager AI interpretation
Ask questions about your results in plain language. Genome Manager uses your sequencing data and the latest clinical literature to help you understand what your variants mean.
Reports updated for life
Your DNA does not change, but science does. As new variant-disease associations are validated, your reports update automatically. One test, permanent and growing value.
Your symptoms are real. The answer may be in your genome.
One kit, sent to your home. Your entire genome sequenced at clinical grade. 200+ physician-ready reports in 6 to 8 weeks. Updated for life as science advances.
From $449
Ships within 48 hours · Results in 6 to 8 weeks
BNPL / HSA / FSA ELIGIBLE