Hi everyone,
I am trying to assess the alignment quality of two aligners.
It seems the samtools pileup command does not give data for every position in the genome.
Specifically, it does not print low coverage regions - coverage <3 from what I can see.
Is there a way to modify this behaviour ?
I see the -l FILE
at
may be helpful?
I want to include _all_ positions in the pileup.
Thanks
I am trying to assess the alignment quality of two aligners.
It seems the samtools pileup command does not give data for every position in the genome.
Specifically, it does not print low coverage regions - coverage <3 from what I can see.
Is there a way to modify this behaviour ?
I see the -l FILE
at
may be helpful?
I want to include _all_ positions in the pileup.
Thanks
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