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Originally posted by NanYu View PostI'm wondering in the postprocess step, if BFAST will do something like: choose the best for F and second best for R within a pair because that is within the expected distance, yet the best for R is in another chromsome.
I know it is a rare scenario and maybe I should not worry about it.
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The complexity of cancer is clearly demonstrated in the diverse ecosystem of the tumor microenvironment (TME). The TME is made up of numerous cell types and its development begins with the changes that happen during oncogenesis. “Genomic mutations, copy number changes, epigenetic alterations, and alternative gene expression occur to varying degrees within the affected tumor cells,” explained Andrea O’Hara, Ph.D., Strategic Technical Specialist at Azenta. “As...-
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