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JaBbA
MIP based joint inference of copy number and rearrangement state in cancer whole genome sequence data.gGnome
R API for browsing, analyzing, and manipulating reference-aligned genome graphs in a GenomicRanges frameworkgGnome.js
gTrack
R package for visualizing complex and multi-track 1D and 2D genomic data in GenomicRanges frameworkdryclean
Irons out wrinkles in noisy coverage data using robust PCAFlow
R-based genomics workflow managementfragCounter
GC and mappability corrected fragment coverage for paired end whole genome sequencingGxG
Scalable GenomicRanges based class for storing, manipulating, and querying genomic matrices and pairwise features.chromunity
Discovery of communities in Pore-C concatemersgUtils
Utility functions to extend and optimize GenomicRanges functionality.skitools
General purpose mskilab R toolsPpurple
Probabilistic purity ploidy estimationMuTrix
R package for visualizing matrices of mutations and other patient level features across patient setsbambi
indexed file format for barcoded BAMs with API for converting and accessing alignment recordsbamUtils
RSeqLib
R interface to SeqLibloosends
Loose ends in cancer genome structurepgv
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