VarSome maintains, harmonizes, and integrates over 130 genomic databases and over 32 million publications to give you the most comprehensive variant interpretation engine there is. The complete list of data sources can be viewed at https://varsome.com/datasources.
Features / strengths
Cited in over 1 700 peer-reviewed publications, VarSome’s proprietary ACMG*, AMP**, and CNV classifiers apply industry standard variant interpretation guidelines to help you understand your variants. Unlike other static platforms, our classifiers are dynamic and work in real-time making it possible to classify even novel variants. To ensure high levels of confidence, VarSome’s classifiers provide transparency on evidence used and rules triggered as well as giving users the ability to adjust rule weighting.
Specification in detail
For labs that only need to look up known variants of interest
For professional users requiring a high volume of queries
For labs generating NGS data needing fast, scalable, and powerful variant interpretation
For Bioinformatics groups needing to integrate the VarSome database and classifiers into existing in-house pipelines