Entering edit mode
7.0 years ago
reza
▴
300
i want to identify CNV using WGS data. i mapped my reads into reference genome and now using Biomedical genomics workbench, i wanna detect CNV in whole genome not targeted region but copy number variation tool in Biomedical genomics workbench require target region track. i read software manual but I did not find anything to help me, what is purpose of target region track. how can i create target region track ?
