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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

MaintainerYuchao Jiang <yuchaoj@wharton.upenn.edu>
AuthorYuchao Jiang, Nancy R. Zhang
LicenseGPL-2
Downloads rank629
Source branchdevel
biocViewsCopyNumberVariation, ExomeSeq, ImmunoOncology, Normalization, QualityControl, Software

Documentation

Download

Follow the installation instructions to use this package in your R session.

Source packageCODEX_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