Exactly. And for those which are controlled with a normal sample, the analysis pipeline is not clear to me.
Let's say for one patient the region chr1:1000-1200 has a seqMean of 0.2 in the normal and 0.7 in the tumor sample. What do I get when download the T and N sample? Reading SNP array-based data, I should get the relative expression, e.g. relativeExpression(N, T) = relativeExpression(0.2, 0.7). But then, why do they still provide the control? And to come back to the somatic SNP example, they solved this issue by providing two identical files for one patient, here the T and N files are the same.
Long story short: What data do I get in each file.