I have the alignment file for my genome (bam).
I want to find out % of genome that covered reference human genome with atleast 1 read, 2 reads, 3 reads, and 4 reads.
How do I go about it?
I want to find out % of genome that covered reference human genome with atleast 1 read, 2 reads, 3 reads, and 4 reads.
How do I go about it?
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