I have two groups of samples, tumor and normal. Now, I want to compare the CNV difference between this two groups.
I windowed the genome in to 10kb bins, and compute the reads number in every bins. I have to normalize the sequence depth and make sure the CNV value in every bin are in the same scale in order to have a valid comparison.
I used HMMcopy to tackle GC bias, but how to scale the different samples into a comparable dimension puzzled me. I know that just normalize sequence depth is not enough.
Is there any software or methods to tackle this problem?
Sorry for not illustrate this in picture, I failed to insert pictures in this post.