Variant Viewer

The purpose of this tool is to provide a way to store, organize, view, and eventually search Variant data from user-uploaded files. Each Study (e.g. a single patient, VIP, etc.) can contain many Samples. Each of these samples may be represented by one or many NGS libraries identified by Bionimbus IDs. The Variant Report resulting from the comparison of 2 Bionimbus IDs, such as a Tumor/Normal pair, can be loaded into this service.

Click here to access Variant Viewer