A bioinformatics best-practice analysis pipeline for calling structural variants (SVs), copy number variants (CNVs) and repeat region expansions (RREs) from short DNA reads
Change the tests to a more unit test/modular approach where each part is tested for all possible inputs and outputs. Only run the whole pipeline in stub form to test the connection between all parts
Description of feature
Change the tests to a more unit test/modular approach where each part is tested for all possible inputs and outputs. Only run the whole pipeline in stub form to test the connection between all parts