Running the variant detection
To start the variant calling:Toolbox | Legacy Tools () | Probabilistic Variant Detection (legacy) ()
This opens a dialog where you can select mapping results ()/ ()/ () or RNA-Seq analysis results ().
Subsections
Toolbox | Legacy Tools () | Probabilistic Variant Detection (legacy) ()
This opens a dialog where you can select mapping results ()/ ()/ () or RNA-Seq analysis results ().