Comments (14)
I think vg simplify
being too old is probably at the root of this particular issue. Please raise an issue on the vg github and we can ask its author @adamnovak if you can even expect it to help you here (probably not).
In general, we want vg to be fully compatible with PGGB. The main issue now (as you're aware, I'm sure) is that the topologies coming out of PGGB are often too complex for vg to index and/or map to effectively. Hopefully there'll be some progress on this in the coming months (it's on all our radars). Unfortunately I don't think vg simplify
, at least in its current state, is the answer. Apart from this issue with mapping, all the vg tools should work (ie for graph maninpulation and stats) should work with PGGB graphs (related - vg can operate directly on GFA without explicitly needing to convert).
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Related Issues (20)
- empty VCF after running PanGenIe on the pggb assembly HOT 1
- GFA with no P lines HOT 5
- DRB1-3123 example not producing a nice graph anymore after `biwflambda` update. HOT 5
- PGGB use case with hexaploidy genomes HOT 1
- force reference output in VCF HOT 2
- Three chromosome take too long time HOT 16
- High heterogeneity in sequences identity HOT 2
- extracting node path-coverage information HOT 3
- wfmash -Y option HOT 3
- About the result study HOT 4
- Question about the example "scerevisiae7.fasta.gz " HOT 1
- ValueError: too many values to unpack (expected 13) HOT 3
- Annotating the 1D pangenome graph visualisation with centromere coordinates
- Get the fasta file of non reference sequence
- [W::vcf_parse] Contig '2' is not defined in the header. (Quick workaround: index the file with tabix.) HOT 4
- PGGB get the fasta file of non reference sequence
- Building a graph from fragmented assemblies
- Current Bioconda release does not find python scripts HOT 7
- Possible community detection bug HOT 5
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