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vgraph is a command line application and Python library to compare genetic variants using variant graphs. ``vgraph`` utilizes a graph representation of genomic variants in to precisely compare comple...

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Is there an available manuscript which describes this tool? I've seen this work cited in recent publications, but only this repository is cited. I ask because I'd like to develop...

Hello, I'm amazed how well `vgraph` works. What I would really like to have, is a way to see, why there is a mismatch between two samples. This can be...

I'd like to use vgraph to compare different "variation" graphs, in the [vg](https://github.com/vgteam/vg) sense. Could vgraph or its algorithms be applied to the DAG-like parts of generic genome graphs?

Hi Kevin, I was looking at some GIAB data this morning and found the link to your tool. I gave it a whirl with this command: `vgraph repmatch --include-regions GIAB/HG001_GRCh37_GIAB_highconf_CG-IllFB-IllGATKHC-Ion-10X-SOLID_CHROM1-X_v.3.3.2_highconf_nosomaticdel.bed...

A fresh install of vgraph on a clean linux system gives the following error: > root@5dda7d88618a:/data#` vgraph > Traceback (most recent call last): > File "/usr/local/bin/vgraph", line 9, in >...

Does vgraph compare gVCFs of various forms? Aside from the standard form on page 24 of gVCF [spec](https://samtools.github.io/hts-specs/VCFv4.3.pdf) where a symbolic alt allele indicates a hom ref block, GATK uses...

Might be nice to have support for VCFs read though URLs instead of files. That way we could annotate against VCFs stored in remote DBs more easily.

In some cases it's handy to be able to compare VCFs without sample information - for instance, to see which variants in some query VCF match those in, say, the...

Hi Kevin, Thanks so much for creating this tool! I made a few trivial changes that makes the setup more universal (hopefully) and lets it work on my mac, for...