Hi,
I am working on targetted ONT long reads, mapping them with minimap2 using the following options
~/apps/minimap2/minimap2 -ax map-ont --secondary=no
And then doing SNP calling using
bcftools mpileup -q 10 -d 75000 -f
I am mapping on 3 distinct references to know which are present, but know that 2 or them are really close (less than 5 SNPs out of 2kb). Using the same bam file, I get drastically different results when using samtools coverage or samtools depth versus bcftools mpileup. Using samtools coverage I get the following:
#rname startpos endpos numreads covbases coverage meandepth meanbaseq meanmapq
ref1 1 3537 7764 3527 99.7173 6959.96 23.5 4.23
ref2 1 3537 1524 3430 96.9748 1298.73 22.5 3.58
ref3 1 3537 1005 3423 96.7769 850.552 22.8 1.36
Using samtools depth I get similar depths. While when I use bcftools mpileup, I get really low coverage (90 to 300 depending on the refs) and a lot of indels, which I know to be fake from looking at the sequences. If I use mapping + SNP calling using mpileup on each reference separately, indels disappear, and I get the right coverages.
I haven't found anything online, but has anyone encountered the same issue? Does anyone have an explanation or knows how to solve that (appart from mapping on each reference individually, which I would rather avoid)?
Thanks a lot!
