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I find the documentation for the use of reference genomes from iGenomes lacking (see https://nf-co.re/rnaseq/3.9/parameters#reference-genome-options). Apart from "GRCh38", which is mentioned in the extended help text, what other "IDs" are valid for this parameter? And which specific reference genome sources do they map to?
It may also be helpful to mention where the reference files get downloaded to (I think work/stage/*/* in the output directory), in case they're needed for further analysis.
The text was updated successfully, but these errors were encountered:
Description of feature
I find the documentation for the use of reference genomes from iGenomes lacking (see https://nf-co.re/rnaseq/3.9/parameters#reference-genome-options). Apart from "GRCh38", which is mentioned in the extended help text, what other "IDs" are valid for this parameter? And which specific reference genome sources do they map to?
I've looked through a lot of documentation and followed a lot of links (e.g. https://nf-co.re/usage/reference_genomes, https://ewels.github.io/AWS-iGenomes/, https://support.illumina.com/sequencing/sequencing_software/igenome.html), but couldn't find a clear answer.
It may also be helpful to mention where the reference files get downloaded to (I think
work/stage/*/*
in the output directory), in case they're needed for further analysis.The text was updated successfully, but these errors were encountered: