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dpryan79 avatar dpryan79 commented on July 22, 2024

I suppose so. Keep in mind, though, that this will end up being per-base (overlapping a CpG) per-read, so the numbers will probably look disturbingly high.

from methyldackel.

avilella avatar avilella commented on July 22, 2024

Great, thanks.

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nchernia avatar nchernia commented on July 22, 2024

Similar question: would it be possible to have some kind of alignment report akin to Bismark's, where sequence pairs that are not used are reported? I.e. some alignments are not used due to low MAPQ or low Phred and some supplementary alignments are discarded; it would be nice to know how many of the sequenced read pairs are used for the methylation calls.

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dpryan79 avatar dpryan79 commented on July 22, 2024

@nchernia I'll see what I can do. The functions that filter reads by MAPQ/flag are buried pretty deep in the code. The phred filtering stuff happens for each base, so I'll try to come up with a reasonably meaningful aggregate value for that.

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