I would like to confirm the definition of the 'reads density' column in the final output file of Ribotricer. Are the 'reads' here not normalized, similar to ‘Counts’ in RNA-seq?
The read density is simply: (number of uniquely mapped reads)/(orf length). I would recommend using DESeq2 or related tools for normalization of the counts matrix.
Hi, saketkc
I would like to confirm the definition of the 'reads density' column in the final output file of Ribotricer. Are the 'reads' here not normalized, similar to ‘Counts’ in RNA-seq?
Thanks, LeeLee