Open SimonaSecomandi opened 5 months ago
Yeah, there are 4 types of graphs, the name conventions apply to all files, but here's an example with .gfa
.
.sv.gfa
: minigraph output -- just SVs and limited path embeddings.gfa
: default/clipped graph -- used for most vg tools.full.gfa
: unclipped full graph -- better for odgi.dX.gfa
: allele frequency filtered graph. was used for read mapping but has been made obsolete by haplotype samplingSo in your .chroms
output, because you ran with --chrom-vg clip filter
and --odgi
(which is the same as --odgi full
) you will get
chr1.vg
: default/clipped graph chr1.full.og
: unclipped/full graphchr1.dX.vg
: allele frequency filtered graph (obsolete -- see above)
Hi all, I generated a pangenome with Minigraph-Cactus with this command:
I have these graphs in the main folder:
The full graph it the one you can use for visualization with odgi, but what is the
3_MC_all.gfa.gz
graph? is this the clipped one?I'm also wondering what to do if I want to analyze each chr separately. I have the chromosome graphs in the
3_MC_all.chroms
subfolder, but they are only infull.og
,.vg
and.d3.vg
formats. However, on the MC paper all the analysis (except short-read mapping) were performed on the clipped graph. So should I split the clipped3_MC_all.gfa.gz
in chrs? Or should I covert the3_MC_all.chroms/chr.vg
chromosome graph in gfa (assuming is clipped)? and why this is not done automatically?And moreover, if I want to run a
vg Giraffe
test on one of the filtered chromosomes, should I generate indexes for3_MC_all.chroms/chr.d3.vg
, or is there another way?Many thanks!! Simona