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Oct 31, 2024 · 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.
CE IVD-certified and HIPAA-compliant platform for variant discovery, annotation, and interpretation of NGS data for whole genomes, exomes, and gene panels, for individual samples, trios, families, and cohorts. More about VarSome Clinical.
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.
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.
11.18 introduces updates in VarSome and VarSome Clinical, including improvements on secondary findings detection, enhanced reports, and more.
Oct 30, 2018 · VarSome.com is a search engine, aggregator and impact analysis tool for human genetic variation and a community-driven project aiming at sharing global expertise on human variants....
Here, we present VarSome, a search engine for hu-man genomic variation which enables users to look up variants in their genomic context, collects data from multiple databases in a central location and most im-portantly, aims to enable the community to freely and easily share knowledge on human variation.
Jun 1, 2019 · 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.
We have now incorporated into VarSome the entire database of PubMed publications relevant to genes and variants. This equates to over 4 million articles related to genomics. Additionally VarSome AI has linked over 150,000 publications to variants and genes that were not previously linked by any other source.
