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I obtained the coverage histogram but I am not able to properly distinguish the to peaks. Please find the attached histogram.
What could be the reason? Which low, mid and high cutoff values should I take?
Cheers
The text was updated successfully, but these errors were encountered:
You're half coverage peak is at 30, the second peak is at 60 (it just looks like a shoulder on the first peak). I'd also recommend using the latest version from https://bitbucket.org/mroachawri/purge_haplotigs/
Hi All,
I'm running purge_haplotigs on my heterozygous diploid-phased assembly (primary + haplotigs) using pacbio reads:
$ minimap2 -ax map-pb p_h.fasta pacbio.fasta -t 30 | samtools sort -@ 30 -m 1G -o aligned.bam -T tmp.aln
$ purge_haplotigs readhist -b aligned.bam -g p_h.fasta -t 30
I obtained the coverage histogram but I am not able to properly distinguish the to peaks. Please find the attached histogram.

What could be the reason? Which low, mid and high cutoff values should I take?
Cheers
The text was updated successfully, but these errors were encountered: