Navigate the NGS
universe with confidence
varvis® is your cloud-based and highly automated turn-key solution for all clinical NGS applications - from NGS panels and whole exomes to whole genomes including cancer diagnostics and carrier screening.
One software solution for all NGS Use Cases
Each NGS application has its own challenges and requirements, tiny gears that have to work together perfectly.
varvis® is your one turnkey solution that integrates into your diagnostic workflow seamlessly including NGS raw data processing, genomics data management, and variant interpretation. The software offers you an intuitive navigation user interface that provides you with convenient filtering options and enables you to easily identify, classify, and report relevant genetic variants. The automated and clinically validated CNV and SNV analyses save you time and costs and with our expert support, onboarding, and training you are all set to go.
Our unique validated CNV analysis with single-exon resolution and convenient QC monitoring allow you to replace conventional CNV detection methods with confidence. Use intuitive filtering options, accelerate WES data analysis, and increase your diagnostic yield.
varvis® enables you to identify rare and causative CNV, SNV, and Indels in a single validated process and to replace conventional ligation-based screening method with one comprehensive approach. Automate your NGS workflow and reduce your turnaround time to minutes.
Conventional liquid biopsy technologies only allow you to monitor specific genomic variations. NGS promises to expand your view to panels of genes while maintaining high sensitivity and precision. This process is complex and requires software tailored to your needs.
Carrier screening aims to determine the carrier status of healthy parents for recessive disorders, including X-linked recessive diseases. Even the most complex scenarios are well covered in a single carrier screening filter in varvis®, so that cases can be solved with just a few clicks.