Hello,
I'm trying to calculate rough copy number changes from our targeted (and generally deep) sequence of 3700 exons. However, I have a pretty substantial GC bias issue occurring in some of my samples. So far, I've just done rough bin normalization rather than a loess normalization. It seems that I can bring my data into the correct range, but that there's still a variance issue. I like what is suggested for corrections in the CNAnorm publication, but I feel unsure of how well it would work for such deep coverage localized to so few locations. Does anyone have any suggestions or thoughts?
Thanks,
anjulka
I'm trying to calculate rough copy number changes from our targeted (and generally deep) sequence of 3700 exons. However, I have a pretty substantial GC bias issue occurring in some of my samples. So far, I've just done rough bin normalization rather than a loess normalization. It seems that I can bring my data into the correct range, but that there's still a variance issue. I like what is suggested for corrections in the CNAnorm publication, but I feel unsure of how well it would work for such deep coverage localized to so few locations. Does anyone have any suggestions or thoughts?
Thanks,
anjulka
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