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I am trying to compare how coverage varies with regard to the epi-transcriptomic modification. When comparing the output of epinano/tombo (generated from the master of pores pipeline) I noticed there is a discrepancy between the coverage represented in the file which has modification information and the coverage when calculated using genomeCoverageBed command from Bedtools.
I was wondering why is that. e.g. the sample_name*.tsv.per.site.var.csv.gz file which looks like.
Hi,
I am trying to compare how coverage varies with regard to the epi-transcriptomic modification. When comparing the output of epinano/tombo (generated from the master of pores pipeline) I noticed there is a discrepancy between the coverage represented in the file which has modification information and the coverage when calculated using genomeCoverageBed command from Bedtools.
I was wondering why is that. e.g. the sample_name*.tsv.per.site.var.csv.gz file which looks like.
has coverage of "332.0" here. But in the bedtools output it shows to be :-
ENST00000291700.9 199 469
Where 199 is the position and 469 is the read depth/coverage.
I was wondering how and why the values above are different. Are they calculated differently or do they mean different things?
Kindly let me know. Thank you!
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