Variant filtering & annotation of processed genomic data according to functional, biological, pathway and disease indication with Annotate.

 

 

Variant Calling

 

Configurable prioritized list of variants from with information on location, functional annotation and QC information.

Variant Identification

 

Identify and verify variant detail against literature or your own knowledgebase.

Clinical Signature

 

Find variant-specific indications from literature references.

Surfacing exhaustive, up to date research and information on clinically relevant variants.

 

Our open annotation framework is a genomic knowledgebase that leverages comprehensive literature reviews and the latest clinical information.

Variant data

Dig deeper with powerful data visualization tools and deep research linking.

 

We give you the tools, data, and information to progressively discover more about the variants found in a patient’s genome. The example shown here is tumor pathway.

 

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