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"title": "nRex: Germline and somatic SNV, InDel and SV discovery workflow.",
"upload_type": "software",
"access_right": "open",
"description": "<a href=\"https://github.com/tobiasrausch/nRex\">nRex</a> is a set of scripts to call germline and somatic single-nucleotide variants, short indels and structural variants. The workflow is primarily for human whole-genome sequencing data (>=30x) using short or long-reads.",