Package: falconx 0.2

Hao Chen

falconx: Finding Allele-Specific Copy Number in Whole-Exome Sequencing Data

This is a method for Allele-specific DNA Copy Number profiling for whole-Exome sequencing data. Given the allele-specific coverage and site biases at the variant loci, this program segments the genome into regions of homogeneous allele-specific copy number. It requires, as input, the read counts for each variant allele in a pair of case and control samples, as well as the site biases. For detection of somatic mutations, the case and control samples can be the tumor and normal sample from the same individual. The implemented method is based on the paper: Chen, H., Jiang, Y., Maxwell, K., Nathanson, K. and Zhang, N. (under review). Allele-specific copy number estimation by whole Exome sequencing.

Authors:Hao Chen and Nancy R. Zhang

falconx_0.2.tar.gz
falconx_0.2.tar.gz(r-4.5-noble)falconx_0.2.tar.gz(r-4.4-noble)
falconx_0.2.tgz(r-4.4-emscripten)falconx_0.2.tgz(r-4.3-emscripten)
falconx.pdf |falconx.html
falconx/json (API)

# Install 'falconx' in R:
install.packages('falconx', repos = c('https://cran.r-universe.dev', 'https://cloud.r-project.org'))

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This package does not link to any Github/Gitlab/R-forge repository. No issue tracker or development information is available.

1.00 score 7 scripts 471 downloads 3 exports 0 dependencies

Last updated 8 years agofrom:efa5f9d657. Checks:OK: 2. Indexed: yes.

TargetResultDate
Doc / VignettesOKNov 12 2024
R-4.5-linux-x86_64OKNov 12 2024

Exports:getASCN.xgetChangepoints.xview

Dependencies: