thanks, i have read this paper before, however, their process to CNV is just a coarse method to transform the level 3 data. I think for more specific, i should look into RAE to build the CNV across each gene, however, i still can not obtain the same data as TCGA offered. Asked the author, however, no response back.
Another question is that when we deal with level2 or level 3 data, which have been already normalized, should we use the tumor intensity - matched normal intensity to obtain a tumor-over-normal one? I suppose TCGA has already done this process?
If you know, could you just give me some points?
And of cource, thank you for sharing the data in the paper you mentioned, though may be rough, but could be quite useful to me. Send the file to jf1986.jiang@gmail.com if you can,
thanks!