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3.6 years ago
puddingmeow516
▴
10
Hi all,
I am currently using vgtools on ancient DNA. My objective is to map reads to the variation graph and call variants using vg. In the past, I used bwa to do the alignments, and remove duplicates (Markduplicates) and calibrate PMD (MapDamage) on the BAM file. However, in the vg workflow, I put in two paired FASTQ file to do the mapping, and then I got a GAM file. I haven't figure out a way to put GAM into further modification.
Any suggestions on dealing with duplicates and PMD using vg?
Many thanks!
Monica
It seems like you want to go from gam to bam using something like this:
vg surject -x x.xg -b aln.gam > aln.bam
Yes exactly, thank you!