Update bam2fastq10x to handle multiplexed samples #6702
Merged
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Changes
Currently, the module expects converted files to be located in the working directory prefixed with a given label. However, converting multiplexed samples result in nested directory structure. The
prefix
argument is used to name the top level directory. In the next level are two directories, one for GEX and one for CMO reads.Thus, the update is simply changing the output path to expect a nested directory and collect all
.fastq.gz
files.PR checklist
Closes #6725
versions.yml
file.label
nf-core modules test <MODULE> --profile docker
nf-core modules test <MODULE> --profile singularity
nf-core modules test <MODULE> --profile conda
nf-core subworkflows test <SUBWORKFLOW> --profile docker
nf-core subworkflows test <SUBWORKFLOW> --profile singularity
nf-core subworkflows test <SUBWORKFLOW> --profile conda