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Feature update

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Cohort analysis in the context of clinical genomics variant interpretation

15.9.2023

As genetic testing is being proven useful and used in ever more areas of medicine where it can instruct disease prevention, medical care, and

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CNV analysis with Euformatics Genomics Hub

29.8.2023

Copy Number Variations (CNVs) refer to alterations in the DNA of a genome that result in cells having an abnormal number of copies of one or more

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OmnomicsNGS Version 2.7 – Explore more NGS features with us

28.4.2022

The omnomicsNGS variant interpretation tool for annotation, classification and reporting has been upgraded to its latest version 2.7 this week in an

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omnomicsNGS version 2.5 – now with upgraded WGS analysis capabilities

18.10.2021

The omnomicsNGS variant interpretation, annotation, classification and reporting tool was upgraded to version 2.5 last week in a release that was

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At the forefront of science

Our latest scientific publication “One byte at a time” is now free to download.

Evidencing the quality of clinical service next-generation sequencing for germline and somatic variants.

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