VarSome Clinical

VarSome Clinical is a CE IVD-certified and HIPAA-compliant platform allowing fast and accurate variant discovery, annotation, and interpretation of NGS data for whole genomes, exomes, and gene panels. VarSome Clinical helps molecular geneticists and clinicians increase the diagnostic yield and support treatment decisions for genetic conditions.

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End-to-End Bioinformatics Solution for Next-Generation Sequencing

Structural Variant Interpretation

Upload your long-read or WGS short-read VCFs and annotate SNVs, indels, CNVs, SVs, and repeat expansions in one unified workspace.

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Why VarSome Clinical?

Long and Short Reads Ready

Upload long-read files from PacBio or ONT, or WGS short-reads VCFs for fast, scalable, evidence-based analysis of your structural variants.

All Variants, One Workspace

Our interactive genomic browser links variants to gene models, transcripts, and relevant annotations, built to streamline clinical workflows.

Comprehensive Data Integration

A massive, cross-referenced variant knowledge base, including data from ClinVar, DECIPHER, and DGV, live links to publications, and in silico predictors - designed to guide clinical interpretation.

More than 5000 organizations and a growing community of 500 000 on the VarSome suite!

Member of Global Alliance

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Interested in our Solutions?

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