recipe bioconductor-cnvpanelizer

Reliable CNV detection in targeted sequencing applications

Homepage

https://bioconductor.org/packages/3.11/bioc/html/CNVPanelizer.html

License

GPL-3

Recipe

/bioconductor-cnvpanelizer/meta.yaml

Links

biotools: cnvpanelizer, doi: 10.1038/nmeth.3252

A method that allows for the use of a collection of non-matched normal tissue samples. Our approach uses a non-parametric bootstrap subsampling of the available reference samples to estimate the distribution of read counts from targeted sequencing. As inspired by random forest, this is combined with a procedure that subsamples the amplicons associated with each of the targeted genes. The obtained information allows us to reliably classify the copy number aberrations on the gene level.

package bioconductor-cnvpanelizer

Versions

1.20.0-0,  1.18.0-0,  1.16.0-1,  1.14.0-0,  1.12.0-0,  1.8.0-0

Depends

• bioconductor-exomecopy >=1.34.0,<1.35.0

• bioconductor-genomeinfodb >=1.24.0,<1.25.0

• bioconductor-genomicranges >=1.40.0,<1.41.0

• bioconductor-iranges >=2.22.0,<2.23.0

• bioconductor-noiseq >=2.31.0,<2.32.0

• bioconductor-rsamtools >=2.4.0,<2.5.0

• bioconductor-s4vectors >=0.26.0,<0.27.0

• r-base >=4.0,<4.1.0a0

• r-foreach

• r-ggplot2

• r-gplots

• r-openxlsx

• r-plyr

• r-reshape2

• r-shiny

• r-shinyfiles

• r-shinyjs

• r-stringr

• r-testthat

Required By

Installation

With an activated Bioconda channel (see 2. Set up channels), install with:

conda install bioconductor-cnvpanelizer

and update with:

conda update bioconductor-cnvpanelizer

or use the docker container:

docker pull quay.io/biocontainers/bioconductor-cnvpanelizer:<tag>

(see bioconductor-cnvpanelizer/tags for valid values for <tag>)

Link to this page

Render an badge with the following MarkDown:

[![install with bioconda](https://img.shields.io/badge/install%20with-bioconda-brightgreen.svg?style=flat)](http://bioconda.github.io/recipes/bioconductor-cnvpanelizer/README.html)