i was wondering how tailfindr calculate the average nucleotide translocation rate, which is the value used for the normalization.
I read the paper, but don't really understand what it means, samples per nucleotide. What does one regards here as sample? are these the single, unique reads mapped at each specific nucleotide position?
i was wondering how
tailfindr
calculate the average nucleotide translocation rate, which is the value used for the normalization.I read the paper, but don't really understand what it means,
samples per nucleotide
. What does one regards here as sample? are these the single, unique reads mapped at each specific nucleotide position?thanks