NEW YORK (GenomeWeb) – Finnish bioinformatics firm Euformatics announced today that it has received CE Marking for omnomicsNGS, a tool that helps labs interpret genetic variants and make clinical decisions.

The tool can help determine whether individual variants can have an effect on a patient's disease risk, or response to drugs or treatment, the company said. It performs variant annotation using the most recent disease-specific translational research and user-provided knowledge.

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