Closed sanjaynagi closed 1 year ago
CNV support would be a bit hacky, as there are a few different ways CNVs can appear - different orientations, sometimes other bits of DNA are amplified too, etc.
We should perhaps allow users to provide their own DNA sequence to target (which could contain a CNV), and then use the gget BLAT alignment to find where the primers are on AgamP3.
Far too involved, closing.
Need to figure out the possible CNV orientations. this would possibly require manually providing the cnv sequence and breakpoints