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VarSome is a variant knowledge community, data aggregator and variant data discovery tool.
VarSome.com is a community-driven project aimed at sharing global expertise on human genomic variants. It features a variant search engine and aggregated knowledge base consisting of more than 140 cross-referenced data resources, as well as real-time functional annotation of any variant.
Jun 1, 2019 · VarSome is a search engine for human genomic variation. Users can search by gene name, transcript symbol, genomic location, variant ID or HGVS nomenclature (Dunnen et al., 2016). VarSome can also parse single lines from VCF files to look up the variant they describe.
Oct 30, 2023 · With VarSome Pro you can upload a VCF file containing simple or multiple samples for variant annotation and classification. Subsequently, you can use a sophisticated set of features for browsing and filtering your data.
VarSome Clinical is a clinically-certified platform allowing accurate variant discovery, annotation, and interpretation of NGS data for whole genomes, exomes, and gene panels, which helps molecular geneticists and clinicians reach faster and more accurate diagnoses and treatment decisions for genetic conditions.
With VarSome Pro you can upload a VCF file containing simple or multiple samples for variant annotation and classification. Subsequently, you can use a sophisticated set of features for browsing and filtering your data.
Here you can find some first useful information to help you begin your journey with VarSome Clinical. How do I register for VarSome Clinical? Read More How.
VarSome Picks is an advanced algorithmic filter, designed to empower bioinformatic analysis of genomic variants using AI. This tool goes beyond conventional variant prioritization methods by considering essential parameters such as phenotype, gene, and variant data, all within a disease-specific context.
VarSome Support Center helps you to find FAQ, how-to guides and step-by-step tutorials.
Oct 30, 2018 · VarSome is both a powerful annotation tool and search engine for human genomic variants, and a platform enabling the sharing of knowledge on specific variants. Since its initial release in May 2016, VarSome has grown to 56 000 users from more than 120 different countries.
