NEWS

We are happy to announce that SEQNEXT Version 5.2.0 has been improved for analysis of Virus NGS data.

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The improved algorithm has an accuracy of 96.4%, which was trained on approximately 200.000 real splice sites taken from GRCh37 and 300.000 false...

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CUSTOMER REVIEW

  • 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    If you only have one patient it might not be published at all.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."