Navigate the NGS universe with confidence
varvis® technical workshop @GfH 2022 - March 17, 2022, 11.45-12.45
"Clinical diagnostics beyond the exome: making the most of your NGS data "
presented by Veronika Scholz (MGZ Munich), Dr. Lena Hausdorf (Limbus Medical Technologies) and Dr. Ben Liesfeld (Limbus Medical Technologies)
The varvis® software is the leading software solution for genetic testing laboratories in Germany. When using the varvis® software, laboratories are compliant with international guidelines and well prepared for accreditation of Whole Exome Sequencing assays according to ISO 15189 and for compliance with IVDR.
In this workshop, we will present how the varvis® software enables automated QC and identity checks, fully evaluates all available information, and provides a built-in scalable data-sharing network in compliance with relevant regulations.
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.
Cabinet of curiosities: Detecting and interpreting extraordinary variants with varvis®
Dr. Lena Hausdorf,
Limbus Medical Technologies
Several thousand SNV and CNV analyses are performed every month using the varvis® software in a highly standardized way. 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.
The future is now: a national genomic data network for Germany and beyond
Dr. Ben Liesfeld,
Limbus Medical Technologies
Seven years ago, the varvis® software introduced the reference data network allexes®. It enables genetic testing laboratories to exchange valuable information about millions of genomic variants and related phenotypes. Since then, allexes® has demonstrated that GDPR-compliant large-scale data sharing between private and public institutions alike is not only technically feasible but also enhances the data analysis of every individual patient. We propose to use its blueprint for the national healthcare model project for comprehensive diagnostics using genome sequencing.
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:
LIMITED OFFER
FREE SOFTWARE PREMIUM TRIAL INCLUDING VALIDATION
Are you searching for a complete and compliant CE-IVD software solution for clinical NGS diagnostics? Do you want to establish and validate a high sensitivity assay?
Let's get started and push the boundaries together!
We are offering a free premium trial of our software varvis® including validation for the
first ten applications!
Just use your discount code "varvisGfH2022" in the form below and get the following benefits during your varvis® premium trial:
Analyze two NGS runs
Get detailed QC feedback
Review data in varvis®
Obtain a validation report
Enjoy first-class support