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 complex variants that are refractory to comparison by conventional comparison methods.
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 because a variant is missing in one of the files or the zygosity is different. Currently there is no way to see this different, isn't it?
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 because a variant is missing in one of the files or the zygosity is different. Currently there is no way to see this different, isn't it?fin swimmer