CRAN

rvsel 0.2.1

Rare Variant Selection Procedure

Released May 31, 2016 by Hokeun Sun

This package can be loaded by Renjin but all tests failed.

When a gene or a genetic region is significantly associated with a disease or a trait, the rare variant selection procedure is able to distinguish causal (risk or protective) rare variants from noncausal rare variants located within the same gene or the same genetic region.

Installation

Maven

This package can be included as a dependency from a Java or Scala project by including the following your project's pom.xml file. Read more about embedding Renjin in JVM-based projects.

<dependencies>
  <dependency>
    <groupId>org.renjin.cran</groupId>
    <artifactId>rvsel</artifactId>
    <version>0.2.1-b40</version>
  </dependency>
</dependencies>
<repositories>
  <repository>
    <id>bedatadriven</id>
    <name>bedatadriven public repo</name>
    <url>https://nexus.bedatadriven.com/content/groups/public/</url>
  </repository>
</repositories>

View build log

Renjin CLI

If you're using Renjin from the command line, you load this library by invoking:

library('org.renjin.cran:rvsel')

Test Results

This package was last tested against Renjin 0.9.2689 on Aug 26, 2018.

Source

R
Fortran

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Release History