README.md
In sunny-zq/INGRID: InGRiD: Semi-supervised Identification of Cancer Subgroups using Survival Outcomes and Overlapping Grouping Information
INGRID
INGRID: Integrative Genomics Robust iDentification of cancer subgroups
INGRID is a statistical approach that integrates information from biological pathway databases with high-throughput genomic data to improve the robustness for identification and interpretation of molecularly-defined subgroups of cancer patients.
Installation
To install the development version of INGRID, it's easiest to use the 'devtools' package.
#install.packages("devtools")
library(devtools)
install_github("sunny-zq/INGRID")
Usage
The R package vignette will provide a good start point for the genetic analysis using INGRID package, including the overview of INGRID package and the example command lines:
library(INGRID)
vignette("INGRID-example")
sunny-zq/INGRID documentation built on Oct. 15, 2019, 6:45 p.m.
R Package Documentation
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We want your feedback!
Note that we can't provide technical support on individual packages. You should contact the package authors for that.
INGRID
INGRID: Integrative Genomics Robust iDentification of cancer subgroups
INGRID is a statistical approach that integrates information from biological pathway databases with high-throughput genomic data to improve the robustness for identification and interpretation of molecularly-defined subgroups of cancer patients.
Installation
To install the development version of INGRID, it's easiest to use the 'devtools' package.
#install.packages("devtools")
library(devtools)
install_github("sunny-zq/INGRID")
Usage
The R package vignette will provide a good start point for the genetic analysis using INGRID package, including the overview of INGRID package and the example command lines:
library(INGRID)
vignette("INGRID-example")
R Package Documentation
Browse R Packages
We want your feedback!
Note that we can't provide technical support on individual packages. You should contact the package authors for that.
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