Running the variant detection

To start the variant calling:

        Toolbox | Legacy Tools (Image legacy_tools) | Probabilistic Variant Detection (legacy) (Image snp_detection_legacy_overlay_16_n_p)

This opens a dialog where you can select mapping results (Image contig)/ (Image multicontig)/ (Image read_track_16_n_p) or RNA-Seq analysis results (Image rnaseq).



Subsections