MIP based joint inference of copy number and rearrangement state in cancer whole genome sequence data.
Glocal streaming assembly for somatic and germline structural variant detection.
R package for applying Gamma-Poisson regression to identify statistical enrichment of somatic mutations in regions after correcting for genomic covariates.
R package for visualizing complex and multi-track 1D and 2D genomic data in GenomicRanges framework
R API for building, manipulating, querying, and mining reference-aligned genome graphs within GenomicRanges framework.
D3.js-based dynamic visualization framework of reference-aligned genome graphs and assemblies
Syntactic sugar for GenomicRanges ninjas.
Lightweight R-based genomics workflow management for SGE, UGER, and LSF
GenomicRanges based R class for fast, out-of-core memory access and storage of numeric and character data that is a function of genomic position.
Set of utility functions to access reads, compute coverage, and extract variant sites from BAM files, based on Rsamtools, GenomicRanges and data.table.