Nothing
Method for the calculation of copy numbers and calling of copy number alterations. The algorithm uses coverage data from amplicon sequencing of a sample cohort as input. The method includes significance assessment, correction for multiple testing and does not depend on normal DNA controls. Budczies (2016 Mar 15) <doi:10.18632/oncotarget.7451>.
Package details |
|
---|---|
Author | Jan Budczies, Eva Romanovsky |
Maintainer | Jan Budczies <jan.budczies@med.uni-heidelberg.de> |
License | GPL-3 |
Version | 2.2.2 |
Package repository | View on CRAN |
Installation |
Install the latest version of this package by entering the following in R:
|
Any scripts or data that you put into this service are public.
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.