View source: R/readCNAProfile.R
readCNAProfile | R Documentation |
We used a CNAqc
object, containing a set of mutations, CNA calls and tumor purity values.
The CNAqc was used to deal with the allele-specific CNAs.
readCNAProfile(maf, seg, Patient_ID = NULL, purity = 1, ref = "hg19")
maf |
Maf or MafList object generated by |
seg |
seg or seglist. |
Patient_ID |
Patient_ID: select the specific patients. IF not indicate, the input is Maf and seg, or the input is MafList and segList. |
purity |
purity information for each samples. |
ref |
human reference genome version. Default 'hg19'. Optional: 'hg18' or 'hg38'. |
This code reads the CNA Profiles for each patient. The tumor names of maf and seg are required to match each other.
cnaqc.list for cnaqc initiation.
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