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ICDS: Identification of Cancer Dysfunctional Subpathway with OmicsData

Identify Cancer Dysfunctional Sub-pathway by integrating gene expression, DNA methylation and copy number variation, and pathway topological information. 1)We firstly calculate the gene risk scores by integrating three kinds of data: DNA methylation, copy number variation, and gene expression. 2)Secondly, we perform a greedy search algorithm to identify the key dysfunctional sub-pathways within the pathways for which the discriminative scores were locally maximal. 3)Finally, the permutation test was used to calculate statistical significance level for these key dysfunctional sub-pathways.

Version:0.1.3
Depends:R (≥ 4.3.0)
Imports:igraph,graphite,metap, methods,org.Hs.eg.db
Suggests:knitr,rmarkdown
Published:2024-08-01
DOI:10.32614/CRAN.package.ICDS
Author:Junwei Han [cre], Baotong Zheng [aut], Siyao Liu [ctb]
Maintainer:Junwei Han <hanjunwei1981 at 163.com>
License:GPL-2 |GPL-3 [expanded from: GPL (≥ 2)]
NeedsCompilation:no
Citation:ICDS citation info
Materials:README
In views:Omics
CRAN checks:ICDS results

Documentation:

Reference manual:ICDS.html ,ICDS.pdf
Vignettes:ICDS User Guide (source,R code)

Downloads:

Package source: ICDS_0.1.3.tar.gz
Windows binaries: r-devel:ICDS_0.1.3.zip, r-release:ICDS_0.1.3.zip, r-oldrel:ICDS_0.1.3.zip
macOS binaries: r-release (arm64): not available, r-oldrel (arm64):ICDS_0.1.3.tgz, r-release (x86_64):ICDS_0.1.3.tgz, r-oldrel (x86_64):ICDS_0.1.3.tgz
Old sources: ICDS archive

Linking:

Please use the canonical formhttps://CRAN.R-project.org/package=ICDSto link to this page.


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