If I'm not mistaken, your algorithm adjusted the mutation copy number influenced by the copy number variation described in the published article. Because I am not very familiar with Python, so I am confused about the followed questions:
Is the adjustment of mutation copy number conducted after the inferring of the subclonal tree with MCMC sampling?
Where is the code for the adjustment?
Whether there is a CCF or cellular prevalence value for each mutation?
Hi,
If I'm not mistaken, your algorithm adjusted the mutation copy number influenced by the copy number variation described in the published article. Because I am not very familiar with Python, so I am confused about the followed questions:
Thanks, Liuwei