The varvis® software is
now a certified class C
medical device under IVDR!
Focus on diagnostics
We process the data
Cloud-based genetic diagnostics to accelerate laboratory workflows and enhance patient care.
One turnkey solution for all clinical NGS applications
Solution
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.
![varvis genomics platform - Bioinformatics pipeline](application/files/1315/9317/8804/plugin_varfeed_web.gif)
Bioinformatics
Automated. Validated. Fast.
varfeed® automates the processing of raw next-generation sequencing data from bcl, fastq or bam files. It performs all bioinformatics, including alignment and clinically validated CNV/SNV/Indel variant calling. All results are handed over to varvis® automatically. Pipeline validation is provided as a service – updates are included.
![varvis genomics software](application/files/7115/9317/8918/plugin_varvis_web.gif)
varvis® genomics software
Made for use in clinical diagnostics
varvis® is a clinical decision support system (CDS) and allows you to review, filter, and classify genetic variants. In addition, varvis® is your own comprehensive variant database. It supports the clinical decision-making process and is a registered CE-IVD device according to directive 98/79/EC.
![varvis genomics platform - Annotation](application/files/2216/0491/7917/plugin_allexes_web-01.png)
Annotation
Always up to date
allexes® provides the data for variant annotation to varvis®. allexes® does not only deliver the most recent versions of public databases, but also provides access to aggregated genomic reference data from all our users compliant with HIPAA and EU regulations.
Key benefits
Automated QC
Important quality metrics are monitored automatically for every single NGS sample, but also across batches over time. Don't waste a moment on manual QC.
Push the button
Convenient filtering options such as inheritance filters and virtual panels allow you to filter from thousands of detected SNVs and CNVs. Within seconds.
80% savings
Our clinically validated CNV analysis provides significant time and cost savings compared to ligation based CNV detection methods.
Overnight express
No matter how many samples or how many sequencing runs you have: our fully automated process delivers results overnight. Guaranteed.
Use cases
NGS panels
Identify rare and causative SNV and CNV in a single validated process and replace conventional PCR-based methods.
Whole exome
sequencing
Do you need more than 15 minutes to interpret a whole exome? Accelerate WES interpretation by combining phenotype, family and inheritance information.
Liquid biopsy
Detect somatic variants with validated high sensitivity using state-of-the-art molecular barcoding technologies.
Carrier screening
Even the most complex scenarios are well covered in a single carrier screening filter in varvis® to solve your cases with just a few clicks.
See for yourself how varvis® can accelerate your laboratory workflows and increase your diagnostic yield.
Testimonials
![Prof. Martin Zenker, MD](application/files/9515/8973/9967/zenker.jpg)
University of Magdeburg
![Prof. Rami Jamra, MD](application/files/8015/8973/9965/abou_jamra.jpg)
University of Leipzig
![Dr. Heyko Skladny](application/files/6115/8973/9966/skladny.jpg)
Synlab Zentrum für Humangenetik Mannheim
![PD Dr. Silke Kaulfuß](application/files/5615/9049/4837/Silke_Kaulfuss_testimonial.jpg)
University of Göttingen
![Dr. Sandra Fleischer](application/files/1817/1215/3057/Testimonial_SFleischer.jpg)
Gemeinschaftspraxis für Humangenetik & Genetische Labore Hamburg
Read more
![varvis® blog - The varvis® Software: The first genomics end-to-end software certified as IVDR Class C device varvis® blog - The varvis® Software: The first genomics end-to-end software certified as IVDR Class C device](application/files/6517/1923/9566/varvis-Blog_first-genomics-end-to-end-software-Class-C.png)
The varvis® Software: The first genomics end-to-end software certified as IVDR Class C device
by Dr. Ben Liesfeld, May 31, 2024
Genetic diagnostic laboratories now have access to the first complete genomics software solution which is certified as a Class C device under IVDR. This will significantly reduce the effort required for legally compliant documentation of in-house tests.
![varvis® blog - Q&A: The role of the IVDR conformity assessment in genetic diagnostics varvis® blog - Q&A: The role of the IVDR conformity assessment in genetic diagnostics](application/files/8517/1923/9216/varvis-Blog_Q-A_role-of-IVDR.png)
Q&A: The role of the IVDR conformity assessment in genetic diagnostics
by Dr. Ben Liesfeld & Dr. Sonja Strunz,
May 31, 2024
Now that the regulation on in-vitro diagnostic devices (IVDR) explicitly regulates in-house devices, or laboratory-developed tests (LDTs), in the European Union, the selection of properly CE-labeled devices is increasingly important to health institutions like genetic testing laboratories.'
![varvis® blog - The varvis® onboarding process varvis® blog - TThe varvis® onboarding process](application/files/8917/1923/9215/varvis-Blog-Onboarding-process.png)
The varvis® onboarding process
by Dr. Roberta Trunzo, April 16, 2024
Welcome to the varvis® software! We understand that, as a new customer, navigating through a new software platform can be overwhelming. That’s why we’ve created this comprehensive guide to get an overview of all the steps in the process. Our mission? To facilitate a smooth onboarding to our reliable and high-performance varvis® software and this step-by-step walk-through will ensure you make the most out of it.