mskilab/JaBbA: Infer cancer graph genomes from read depth and junctions

JaBbA simultaneously infers integer copy numbers for genomic segments and their connections based on the read depth and the graph structure defined by the structural variations identified from WGS data. Two essential inputs are 1) a high-density read depth ratio between tumor and normal samples (we also have guidelines for the cases lacking paired normal sequencing) and 2) the putative somatic structural variations. The output is a somatic rearrangement graph representing the integer copy numbers of DNA segments and their connections. The output is a copy number annotated genome graph.

Getting started

Package details

Bioconductor views bioc::3.15/DNAcopy bioc::3.15/GenomeInfoDb bioc::3.15/GenomicRanges bioc::3.15/S4Vectors bioc::3.15/VariantAnnotation bioc::3.15/rtracklayer
Maintainer
LicenseMIT + file LICENSE
Version1.1
Package repositoryView on GitHub
Installation Install the latest version of this package by entering the following in R:
install.packages("remotes")
remotes::install_github("mskilab/JaBbA")
mskilab/JaBbA documentation built on June 9, 2024, 12:40 p.m.