Description of the bug
When specifying two or more of mutations, cnas, translocations, for the same sample (each in one row in the samplesheet), they get queried individually, overwriting the previous results.
Probably due to output files having the same name.
potential fixes:
- join channels / group by sample so that a single query containing all variant types can be submitted
- set output names depending on variant type
- ...
Command used and terminal output
nextflow run qbic-pipelines/variantmtb -r dev -profile docker -params-file params.yml
Relevant files
input_SNPs-CNAs.csv
params.yml
input : "input_SNPs-CNAs.csv"
outdir : "variantmtb_debug_out"
genome : "GRCh37"
databases : "cgi"
cgi_cancer_type : "Any cancer type"
System information
No response