So is it advisable to compare normal vs tumor and find the variants for this sample?
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I have one tumor/normal WGS data from a breast cancer patient and the tumor bam file is 11.2 GB in size, while the normal bam file is 27.6 GB in size. Isn't this uncommon, considering tumor files are usually larger than normal ones?
It's a bit unusual to sequence a normal sample 2.5x as deep as the cancer sample that you're more interested in, yes. It's quite possible that the normal sample was on a different run or machine, where there was more space (and thus more total reads).
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