Hi. I have downloaded the corresponding mutation and CNV data from DepMap version 21Q4. For the CNV data (CCLE_gene_cn.csv), the data description is “Gene level copy number data, log2 transformed with a pseudo count of 1. This is generated by mapping genes onto the segment level calls”, which I couldn't understand clearly. What I understand is that the value generated by adding 1 to all the original copy number values and then log2-transformed. Another question is why they add the value of 1 before transforming the copy number data. How to interpret the copy number status (deep deletion, het loss, diploid, gain and amplified) from the CCLE copy number data?
Hi! Did you find answer to this question?
No. I'm still expecting an answer.
Have you find the answer yet? Because I am looking for the same question