A bioinformatics best-practice analysis pipeline for calling structural variants (SVs), copy number variants (CNVs) and repeat region expansions (RREs) from short DNA reads
Remove all mentions of params in the workflows and add them all as inputs to the workflows/subworkflows
Emit all sensible outputs from the main workflow too
Description of feature
Remove all mentions of
params
in the workflows and add them all as inputs to the workflows/subworkflows Emit all sensible outputs from the main workflow too