ActiveDriverWGS
A Driver Discovery Tool for Cancer Whole Genomes
v1.2.1
·
Mar 13, 2026
·
GPL-3
Description
A method for finding enrichments of somatic single nucleotide variants (SNVs) and small insertions-deletions (Indels) in functional elements in the human genome. 'ActiveDriverWGS' detects coding and noncoding cancer driver elements using whole genome sequencing data. The method is part of the publication H. Zhu et al. (2020) <doi:10.1016/j.molcel.2019.12.027> "Candidate Cancer Driver Mutations in Distal Regulatory Elements and Long-Range Chromatin Interaction Networks" in Molecular Cell.
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Show all 14 flavors
| Flavor | Status |
|---|---|
| r-devel-linux-x86_64-debian-clang | OK |
| r-devel-linux-x86_64-debian-gcc | OK |
| r-devel-linux-x86_64-fedora-clang | OK |
| r-devel-linux-x86_64-fedora-gcc | OK |
| r-devel-macos-arm64 | OK |
| r-devel-windows-x86_64 | OK |
| r-oldrel-macos-arm64 | NOTE |
| r-oldrel-macos-x86_64 | NOTE |
| r-oldrel-windows-x86_64 | OK |
| r-patched-linux-x86_64 | OK |
| r-release-linux-x86_64 | OK |
| r-release-macos-arm64 | OK |
| r-release-macos-x86_64 | OK |
| r-release-windows-x86_64 | OK |
Check details (2 non-OK)
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package dependencies
Packages suggested but not available for checking: 'BSgenome.Hsapiens.UCSC.hg19', 'BSgenome.Hsapiens.UCSC.hg38', 'BSgenome.Mmusculus.UCSC.mm9', 'BSgenome.Mmusculus.UCSC.mm10'
NOTE
r-oldrel-macos-x86_64
package dependencies
Packages suggested but not available for checking: 'BSgenome.Hsapiens.UCSC.hg19', 'BSgenome.Hsapiens.UCSC.hg38', 'BSgenome.Mmusculus.UCSC.mm9', 'BSgenome.Mmusculus.UCSC.mm10'
Changelog
Full NEWS →v1.2.1
# ActiveDriverWGS 1.2.1
• Bug fixed: elements and sites with coordinates below 2 or beyond the chromosome end now return an informative error, preventing downstream failures in trinucleotide context calculations.
• Bug fixed: all GenomicRanges operations (findOverlaps, setdiff, intersect, union) now use ignore.strand = TRUE, ensuring mutations, elements, and sites are always matched by genomic position regardless of strand.
• Bug fixed: elements and sites with coordinates below 2 or beyond the chromosome end now return an informative error, preventing downstream failures in trinucleotide context calculations.
• Bug fixed: all GenomicRanges operations (findOverlaps, setdiff, intersect, union) now use ignore.strand = TRUE, ensuring mutations, elements, and sites are always matched by genomic position regardless of strand.
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NOTE 4 OK · 1 NOTE · 0 WARNING · 0 ERROR · 0 FAILURE Mar 13, 2026
NOTE
r-oldrel-macos-arm64
package dependencies
Packages suggested but not available for checking: 'BSgenome.Hsapiens.UCSC.hg19', 'BSgenome.Hsapiens.UCSC.hg38', 'BSgenome.Mmusculus.UCSC.mm9', 'BSgenome.Mmusculus.UCSC.mm10'
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Version History
new
1.2.1
Mar 13, 2026