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Description
In the output of dmr multi
there are columns such as samplea_counts
and sampleb_counts
. Given that the command is given sample names it would be nice if the file itself contained pairings between A, B and the sample names. Currently this relies on the user ensuring they don't modify the sample name. Perhaps this is not very practical if we're following any standards though, and that would be understandable in which case perhaps a comment at the top of the file?
PS: What is the difference between the nucleotide count and Total number of base modification calls in the region, including unmodified, for sample A
for the output column samplea total
? Is it because some nucleotides don't pass the threshold to be confidently called as unmodified?