I have RNA-seq data in terms of aligned reads.
Now I just want to quantify the read counts per bp w/o the consideration of the overlap w/ any feature (example result file [1]). How can I do that?
[1] http://www.ebi.ac.uk/arrayexpress/fi....basecount.txt
Now I just want to quantify the read counts per bp w/o the consideration of the overlap w/ any feature (example result file [1]). How can I do that?
[1] http://www.ebi.ac.uk/arrayexpress/fi....basecount.txt
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