Navigate the NGS universe with confidence


Join us for our Workshop

Friday, September 9   |   12.30 - 13.30   |   SALA A

& visit us at Booth #17

Join us for SIGU 2022

We are looking forward to three days full of interesting and exciting talks, presentations and workshops at SIGU 2022 in Trieste, September 7-9. We invite you to join us and our three experts for our workshop "Exome diagnostics and beyond" on Friday, September 9, and to visit the varvis® team at our booth #17 to have a chat, discuss the latest advancements and get a deeper look into the varvis® software and its new features.


September 9




varvis® corporate satellite 

"Exome diagnostics and beyond: Making the most of your clinical NGS data"

Large NGS-based panels or even Whole Exome Sequencing have become the first-line diagnostics in most European countries. This has led to the generation of huge amounts of data that need to be processed, assessed, and interpreted with confidence. With the varvis® software alone, several thousand patient samples are analyzed every month in a highly standardized way. With the right toolset, the analysis of an exome often has become a matter of minutes. Still, there are the simple and the more complicated cases.

In this workshop, our speakers will present how the varvis® software facilitates automated QC and identity checks and enables you to quickly solve even complex cases by fully evaluating all available information.

Our speakers & talks

Automated quality control: a must-have for accreditation and to accelerate the NGS workflow

Veronika Scholz,
MGZ Munich

Regulations and guidelines impose many requirements on the workflows in genetic testing laboratories. High-throughput laboratories rely on automating processes and reducing hands-on time. Here we present how MGZ München utilizes the varvis® Validation Service and the API to automate crucial processes in quality control including identity checks and the detection of maternal contamination based on NGS data alone.

How software can help solve whole exomes

Marija Vesic,
SYNLAB MVZ Humangenetik Mannheim GmbH

A validated and automated software solution enhances the diagnostic yield of WES-based genetic testing. Using real clinical examples, we will present how the genomics platform varvis® enables us to quickly solve even complex cases e. g. by providing convenient inheritance filters and phenotype-based variant prioritization.

Cabinet of curiosities: Detecting and interpreting extraordinary variants with varvis®

Dr. Lena Hausdorf,
Limbus Medical Technologies GmbH

Together with our customers, our support team endeavors to understand puzzling results or apparent contradictions with other methods. We will illustrate and explain a selection of unexpected and illuminating discoveries that highlight the great value of the comprehensive analysis of NGS data.

varvis® - Navigate the NGS universe with confidence

Cloud-based genetic diagnostics to accelerate laboratory workflows and enhance patient care

The varvis® genomics platform is a complete solution for clinical diagnostics, supporting NGS raw data processing, genomics data management, and variant interpretation. Automated CNV and SNV analysis are clinically validated and completely integrated into the NGS workflow. It is your one turnkey software solution for all NGS Panels, cancer diagnostics, WES and WGS.

Click here to learn more about how varvis® can accelerate your laboratory workflows and increase your diagnostic yield:

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