Hello, Aaron and everyone - Thanks for the great tools you guys have created!
We have some high coverage panel sequencing data, but checking the depth of the regions using mosdepth, bedtools and sambamba, give quite a range of results (results obtained running these commands through snakemake file).
These tools are run with the default setting, what might cause such a huge difference in depth calculations? Are there some filtering or duplicate reads filtering in bedtools for bedtools coverage -mean calculation?
Hello, Aaron and everyone - Thanks for the great tools you guys have created!
We have some high coverage panel sequencing data, but checking the depth of the regions using mosdepth, bedtools and sambamba, give quite a range of results (results obtained running these commands through snakemake file).
These tools are run with the default setting, what might cause such a huge difference in depth calculations? Are there some filtering or duplicate reads filtering in bedtools for
bedtools coverage -mean
calculation?Thanks in advance!