Move to main content
Euformatics logo
  • Frontpage
  • Genomics Hub
    • Gene Test ValidationQuickly validate your pipeline
    • Sample Quality ControlControl sample quality with ease
    • Variant InterpretationRelevant variants and reports within minutes
  • Full Stack AI
  • News
  • About us
    • Our mission
    • Team
  • Careers
  • Contact us
  • Book a demo
Book a demo

News

Show AllEuformatics BlogFeature updateNews

CSO Christophe Roos discusses clinical application of NGS in Medical Laboratory Observer

28.6.2016

Next-generation sequencing, with other technologies, is enabling the emergence of nucleic acid -based testing in the clinical lab. The article in

Read more

EMQN & UK NEQAS quality assessment scheme seeks to improve NGS in diagnostic labs

16.6.2016

Euformatics’ partners EMQN and UK NEQAS for Molecular Genetics are currently developing the 2016 quality assessment, which NGS labs will be able

Read more

Euformatics offers training at the ELIXIR EXCELERATE CSC course on variant interpretation

11.6.2016

This ELIXIR EXCELERATE course, organised by CSC, covers several aspects of variant analysis including variant annotation and prioritisation.

Read more

EMQN, UK NEQAS for Molecular Genetics, and Euformatics gear up for EQA 2016 Pilot

10.6.2016

The team from UK NEQAS for Molecular Genetics and the European Molecular Genetics Quality Network EMQN visited Euformatics to prepare for this

Read more

EMQN, UK NEQAS for Molecular Genetics, and Euformatics talk about standardising NGS quality control at ESHG

12.5.2016

NGS External Quality Assessment Participants Meeting at ESHG 2016 At the joint UK NEQAS for Molecular Genetics and EMQN Participants meeting the

Read more

Euformatics CSO Christophe Roos talks to GenomeWeb

25.2.2016

On the heels of the announcement about the CE mark for Euformatics’ omnomicsNGS tool for genome variant interpretation, Christophe addresses

Read more

Euformatics receives CE mark for omnomicsNGS

23.2.2016

Euformatics has received CE Marking for omnomicsNGS, a tool that helps labs interpret genetic variants and make clinical decisions. The tool can

Read more

Previous page 1 … 10 11 12 13 14 Next page

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.

  • This field is for validation purposes and should be left unchanged.

Brought to you by:

EMQN logo

Discover the potential of automated NGS data processing

Book a demo
Contact our experts

Gene Test Validation

Learn more

Sample Quality Control

Learn more

Variant Interpretation

Learn more

Euformatics logo

Accelerating the transition to precision medicine

More about us

  • Genomics Hub
    • Sample Quality Control
    • Assay Validation
    • Variant Interpretation
  • About us
    • Our mission
    • Team
    • Privacy Policy
  • Careers
  • News
  • Youtube
  • Twitter
  • LinkedIn

All rights reserved © Euformatics2025 | Website by Sivututka