Open ManuelTgn opened 11 months ago
Hi @ManuelTgn,
since I don't know in detail how you created the graphs, it is hard to tell. In ODGI's variation graph model all paths are equal, there is no sense of a reference
path.
If you want to use ODGI to translate path positions to your path of choice, please take a look at https://odgi.readthedocs.io/en/latest/rst/tutorials/navigating_and_annotating_graphs.html#path-to-path-position-mapping.
Hi @subwaystation,
thank you for the reply. That was very helpful!
I created my input graph using the vg
toolkit, enriching a chromosome with some variants stored in a phased VCF. Are there python functions in ODGI's API to replicate the command line functionalities showed in the documentation page you shared?
Hi @ManuelTgn,
I see, so no crazy variants with crazy repeats. That's good :)
As far as I know, the Python API only exposes basic ODGI functionality. You would have to build such code on your own. Take a look at https://github.com/pangenome/odgi/blob/de70fcdacb3fc06fd1d8c8d43c057a47fac0310b/src/subcommand/position_main.cpp#L794-L840 as in inspiration.
Best, Simon
Hi team,
thank you for developing this amazing tool!
I have a couple of questions regarding odgi graphs manipulation through the Python API.
I created an odgi graph from a gfa containing > 1000 haplotypes + 1 reference sequence. Is there a way to understand which path belongs to the reference sequence? All paths seem to point to an haplotype.
While traversing the paths embedded in the graph, is it possible to understand to which position correspond a nucleotide in a node, using the reference coordinates space?
Thanks for the help!