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Pan-genome inference and genotyping with long noisy or short accurate reads

Results 77 pandora issues
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Hi, I am facing an issue regarding the reference path that pandora uses for genotyping the variants. It is basically using the less frequent supported path instead of most frequent...

Mabi got confused by this warning message, and I think the common use case for `pandora` is to actually not receive reference sequences for the genes and automatically infer it...

Placeholder as @Danderson123 keeps saying this and I don't want to lose it. Mapping reads from one sample to a PRG (Ecoli + a few thousand AMR genes) taking 30...

Hello, Thank you for making this useful tool, my question is the following, I would like to know, when i'm making a pangenome from diverse strains of Streptococcus iniae species,...

Downsampling reads is an upstream task, not pandora responsibility

See Zam's comment at https://github.com/rmcolq/pandora/pull/335 Basically, we have several common default CLI args for `compare`, `map` and `discover`, see https://github.com/rmcolq/pandora/blob/master/include/compare_main.h https://github.com/rmcolq/pandora/blob/master/include/map_main.h https://github.com/rmcolq/pandora/blob/master/include/denovo_discovery/discover_main.h Would be better if there was a header...

would make DrPrg accessible to more people

Hey Leandro! I have been taking a look at cases where Pandora incorrectly annotates on gene as another. I took the first allele in each MSA that build my panRG...