Variant data
The Probabilistic Variant Detection and the Quality-based Variant Detection tools identify SNVs (single-nucleotide variants), insertions, deletions or replacements that are presented as variant tracks or in an annotated table.
Subsections
- Variant tracks
- Annotated variant table
- Linking adjacent variants in linkage groups
- Variant types
- Special notes upgrading to Genomics Workbench 6.0