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nf-cmgg
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structural
A bioinformatics best-practice analysis pipeline for calling structural variants (SVs), copy number variants (CNVs) and repeat region expansions (RREs) from short DNA reads
https://nf-cmgg.github.io/structural/
MIT License
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Copy samplesheet in output directory
#83
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nvnieuwk
opened
5 months ago
nvnieuwk
commented
5 months ago
Description of feature
See title
Description of feature
See title