biDNAcopy.findCNVs | R Documentation |
biDNAcopy.findCNVs
classifies the binned read counts into several states which represent copy-number-variation using read count information from both strands.
biDNAcopy.findCNVs(binned.data, ID = NULL, CNgrid.start = 0.5)
binned.data |
A GRanges-class object with binned read counts. |
ID |
An identifier that will be used to identify this sample in various downstream functions. Could be the file name of the |
CNgrid.start |
Start parameter for the CNgrid variable. Very empiric. Set to 1.5 for normal data and 0.5 for Strand-seq data. |
An aneuHMM
object.
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