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  "Title": "A Driver Discovery Tool for Cancer Whole Genomes",
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  "Description": "A method for finding enrichments of somatic single\nnucleotide variants (SNVs) and small insertions-deletions\n(Indels) in functional elements in the human genome.\n'ActiveDriverWGS' detects coding and noncoding cancer driver\nelements using whole genome sequencing data. The method is part\nof the publication H. Zhu et al. (2020)\n<doi:10.1016/j.molcel.2019.12.027> \"Candidate Cancer Driver\nMutations in Distal Regulatory Elements and Long-Range\nChromatin Interaction Networks\" in Molecular Cell.",
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      "title": "fix_all_results verifies that the results table has the correct format and p-values",
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    },
    {
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    {
      "page": "ActiveDriverWGS",
      "title": "ActiveDriverWGS is a driver discovery tool for simple somatic mutations in cancer whole genomes",
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