80% of rare disease has genomic roots. For this reason, discover what our DNA has to say could be crucial to understand our health situation and achieve a diagnosys.
The WGS - Whole Genome Sequencing allow us to analysize the entire DNA (both Exome and Genome) in order to look at the most complete genomic make up and araise as much possible the canche to end a dyagnostic odyssey.
Safe and fast delivery, just purchase the kit and activate it using the Kit ID before testing.
Activate your test & provide your saliva sample in just few minutes.
Receive within weeks digital results of your WGS test displayed in specific reports to help you better explore rare diseases.
Rare Disease Report
We use proprietary algorithms, our report aims to provide rare diagnostics from genomic data, reducing the need for variant filtering and prioritization.
Find out if you have specific genetic variants that influence the way your body processes more drugs.
Build a personalized treatment plan with the most comprehensive report on the market.
All Pathogenic Variants
Whether your journey has just started or it was years ago, you may not know what the real causes of your illness are, that's why we offer a full analysis panel of variants finding the answers to some features about that you didn't know.
Full Raw Data
Your genome does not change from birth on, but science does. For this reason the Whole Genome Sequencing Test is the best lifetime investment: sequence once, get actionable tools for life! Raw data formats available: FASTQ, BAM and VCF.