Always up to date
Use continuously updated public data from sources like gnomAD
phenotyping using ontologies like HPO to improve the accuracy of your diagnosis.
Access more than 10,000 diligently curated clinical NGS cases including all variants and phenotype descriptions
through our allexes network.
Push the button
Convenient filtering options such as inheritance filters allow you to filter from thousands of detected SNVs and
CNVs. Within seconds.
is a medical device Class
I according to MDD 93/42/EEC and compliant with EU regulations.
One for all
One solution for SNV and CNV for NGS panels of all sizes, including WES and WGS.
Our clinically validated CNV analysis provides significant cost savings compared to
ligation based CNV detection methods.
No matter how many samples or how many sequencing runs you have: our fully automated
process delivers results overnight. Guaranteed.
You initiate raw data upload by pushing a button. We deal with IT, processing and bioinformatics.
First class support
Our services comprise technical support, training, documentation as well as validation following all relevant