Some of the highlights: analysis of Whole Exome Sequencing data, easy and fast definition of big panels...

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We are happy to announce that starting Summer 2018, we have now joined efforts with Roche to offer you the best NGS solution...

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  • Marcel Nelen, Head of the division Genome Diagnostics Radboud University, Nijmegen

    "If there is a discrepancy we want to know who came to this conclusion and why. Thus, contact information is very important. If it is about publishing, the same argument holds true.
    If you only have one patient it might not be published at all. Contact the lab(s) who have identified this rare variant and publish together.
    It may take years to find a second patient in your local hospital."