Hi,
I'm currently working happily with the VarScan2 Copy Number Alteration caller for paired exome seq samples. But i'm still a bit confused about the "markers" in the number of markers output. Anyone knows if those are actual exomes or sequenced regions used as markers for the CBS or anything else i didn't get completely?
Best Ron
I don't know if the markers are supposed to be placed on your gene of copy-number interest, or if you mark a relatively normal area as a sort of normalization.
I have been working happily with Varscan2 and have generated the copynumber data for 10 whole genomes, although I have yet to process it fully. I think you're referring to the Recurrent CNA Identification with CMDS? There is a readme at http://sourceforge.net/projects/cmds/files/ that has some information, but the only reference I see to markers is at the bottom of http://varscan.sourceforge.net/copy-number-calling.html