The Variant Interpretation Company
VarSome's world-leading annotation tools are used by researchers and healthcare professionals around the world to power and speed up variant interpretation.
Ask us about our germline, somatic, and CNV variant classifiers!
Our classifiers work 'on the fly' so we can even classify novel variants that haven't been seen before. Combined with our dynamic filters, this makes us ideally suited to exome and genome analysis by providing you with an excellent first-pass variant filter allowing you to zero in on variants of interest and drastically reduce your variant load.
Want to see it for yourself? We'd be happy to give you a demo of VarSome Clinical - our platform for FASTQ and VCF analysis.
VarSome is the emerging global standard platform for human genome data. With more than 350,000 professional users and 130+ standardized and continuously updated major datasets freely searchable online, VarSome.com is the world's largest community and knowledge base for human genome variant data. VarSome's premium, clinical and API tools further enable anyone and any organization, from individual healthcare professionals to hospitals and pharmaceutical companies, to harness and apply the power of this community and data to improve health and lives worldwide. VarSome is created by Saphetor, a Switzerland-based precision medicine company using bioinformatics to apply human genome data to benefit people.