I have a sample from a cultivated tetraploid and the reference genomes I am working with are the two diploid progenitors. I am running Basic Variant Detection on the sample against one of the diploid references and then I will run it against the other diploid.
Should the ploidy setting be 2 or 4? I thought it should be 2.
CLC is a commercial product, ask their paid support staff.
I agree with asking their support stuff. But as a side note, whatever the ploidy is, I would suggest getting an allele frequency spectra, to get a feel of your data. This is NGS right?