fcgr3bMXL: MXL population data (The 1000 Genomes Project)
In CNVrd2: CNVrd2: a read depth-based method to detect and genotype complex common copy number variants from next generation sequencing data.
Description
Usage
Format
References
Description
This data set includes: segmentation results “resultSegment”,
information copy number “copynumberGroups” of FCGR3B gene.
Usage
1
Format
All results analysed by the CNVrd2 package.
References
CNVrd2 documentation built on Nov. 8, 2020, 5:30 p.m.
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.
Description Usage Format References
Description
This data set includes: segmentation results “resultSegment”, information copy number “copynumberGroups” of FCGR3B gene.
Usage
1 |
Format
All results analysed by the CNVrd2 package.
References
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.
Embedding an R snippet on your website
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.