CODEX
A Normalization and Copy Number Variation Detection Method for Whole Exome Sequencing
Bioconductor version: 3.24 · Package version: 1.45.0
A normalization and copy number variation calling procedure for whole exome DNA sequencing data. CODEX relies on the availability of multiple samples processed using the same sequencing pipeline for normalization, and does not require matched controls. The normalization model in CODEX includes terms that specifically remove biases due to GC content, exon length and targeting and amplification efficiency, and latent systemic artifacts. CODEX also includes a Poisson likelihood-based recursive segmentation procedure that explicitly models the count-based exome sequencing data.
Installation
if (!require("BiocManager", quietly = TRUE))
install.packages("BiocManager")
BiocManager::install("CODEX") Details
| Maintainer | Yuchao Jiang <yuchaoj@wharton.upenn.edu> |
| Author | Yuchao Jiang, Nancy R. Zhang |
| License | GPL-2 |
| Downloads rank | 629 |
| Source branch | devel |
| biocViews | CopyNumberVariation, ExomeSeq, ImmunoOncology, Normalization, QualityControl, Software |
Documentation
Download
Follow the installation instructions to use this package in your R session.
| Source package | CODEX_1.45.0.tar.gz |
| Windows binary (x86_64) | CODEX_1.45.0.zip |
| macOS binary (arm64) | CODEX_1.45.0.tgz |
| macOS binary (x86_64) | CODEX_1.45.0.tgz |
Dependencies
Depends: R (>= 3.2.3), Rsamtools, GenomeInfoDb, BSgenome.Hsapiens.UCSC.hg19, IRanges, Biostrings, S4Vectors
Suggests: WES.1KG.WUGSC
Reverse dependencies
Depends On Me (1): iCNV