New ERGO Feature: Affected Features for Variants

When you add annotated BCF or VCF files to ERGO, it automatically computes variant metrics, including the features that have been affected. Easily find which genomic features are affected by variation by clicking on the “Affected Features” tab. From here you can search for your feature or function of interest and see which features have been affected. Clicking on the arrow reveals more information about the feature, including which pathways it is in and which variants have affected this feature.