A method for finding an enrichment of cancer simple somatic mutations (SNVs and Indels) in functional elements across the human genome. 'ActiveDriverWGS' detects coding and noncoding driver elements using whole genome sequencing data.
|Author||Helen Zhu [aut, cre], Juri Reimand [aut]|
|Maintainer||Helen Zhu <[email protected]>|
|Package repository||View on CRAN|
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