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new module: VarScan
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Further Information
VarScan is a variant caller (https://github.com/dkoboldt/varscan) that can do somatic, germline and CNV calling. Recently, there was a published benchmarking study (https://doi.org/10.1093/bib/bbae697), that proposes best combinations of variant callers to use. Following up on the study, I want to implement this into nf-core/sarek, for that I need to include this new variant caller.
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