A bioinformatics best-practice analysis pipeline for calling structural variants (SVs), copy number variants (CNVs) and repeat region expansions (RREs) from short DNA reads
Conda isn't supported for all modules for now (especially qdnaseq is missing a conda declaration for now). This should be fixed to increase the usability of the pipeline
Description of the bug
Conda isn't supported for all modules for now (especially qdnaseq is missing a conda declaration for now). This should be fixed to increase the usability of the pipeline
Command used and terminal output
No response
Relevant files
No response
System information
No response