New release: omnomicsNGS version 2.14.0 brings Patient Identity Vigilance as a new feature
Key highlights We are introducing omnomicsNGS version 2.14 with two new Vigilance features, Identity and Biological Sex, and harmonise them with
New release: omnomicsNGS version 2.13.0 brings ClinGen-aligned somatic classification, enhanced CIViC annotations, structural variant analysis, and support for VCFs from more variant callers
Key Highlights We are now introducing omnomicsNGS version 2.13.0, bringing full support for somatic variant classification using the
Cohort analysis in the context of clinical genomics variant interpretation
As genetic testing is being proven useful and used in ever more areas of medicine where it can instruct disease prevention, medical care, and
CNV analysis with Euformatics Genomics Hub
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
OmnomicsNGS Version 2.7 – Explore more NGS features with us
The omnomicsNGS variant interpretation tool for annotation, classification and reporting has been upgraded to its latest version 2.7 this week in an
omnomicsNGS version 2.5 – now with upgraded WGS analysis capabilities
The omnomicsNGS variant interpretation, annotation, classification and reporting tool was upgraded to version 2.5 last week in a release that was
