BaalChIP
BaalChIP: Bayesian analysis of allele-specific transcription factor binding in cancer genomes
Bioconductor version: 3.24 · Package version: 1.39.0
The package offers functions to process multiple ChIP-seq BAM files and detect allele-specific events. Computes allele counts at individual variants (SNPs/SNVs), implements extensive QC steps to remove problematic variants, and utilizes a bayesian framework to identify statistically significant allele- specific events. BaalChIP is able to account for copy number differences between the two alleles, a known phenotypical feature of cancer samples.
Installation
if (!require("BiocManager", quietly = TRUE))
install.packages("BiocManager")
BiocManager::install("BaalChIP") Details
| Maintainer | Ines de Santiago <inesdesantiago@gmail.com> |
| Author | Ines de Santiago, Wei Liu, Ke Yuan, Martin O'Reilly, Chandra SR Chilamakuri, Bruce Ponder, Kerstin Meyer, Florian Markowetz |
| License | Artistic-2.0 |
| Downloads rank | 458 |
| Source branch | devel |
| biocViews | Bayesian, ChIPSeq, Sequencing, Software |
Documentation
Download
Follow the installation instructions to use this package in your R session.
| Source package | BaalChIP_1.39.0.tar.gz |
| Windows binary (x86_64) | BaalChIP_1.39.0.zip |
| macOS binary (arm64) | BaalChIP_1.39.0.tgz |
| macOS binary (x86_64) | BaalChIP_1.39.0.tgz |
Dependencies
Depends: R (>= 3.3.1), GenomicRanges, IRanges, Rsamtools
Imports: GenomicAlignments, GenomeInfoDb, doParallel, parallel, doBy, reshape2, scales, coda, foreach, ggplot2, methods, utils, graphics, stats
Suggests: RUnit, BiocGenerics, knitr, rmarkdown, BiocStyle