Annotate from Known Variants

To run the Annotate from known variants tool, go to:

        Toolbox | Resequencing Analysis (Image resequencing) | Variant Annotation (Image variant_annotate_folder_closed_16_h_p) | Annotate from Known Variants (Image filter_database_variations_16_n_p)

This tool will create a new track with all the experimental variants including added information about overlapping variants found in the track of known variants. The annotations are marked in three different ways:

For exact matches, all the information about the variant from the known variants track is transferred to the annotated variant. For partial matches and overlaps, the information from the known variants are not transferred.