ExomeDepth-package: Read depth based CNV calls for exome DNA sequence data

In drramki-chop/edm: Scalable workflow to identify copy Number variants from exome sequencing data

Description

ExomeDepth uses read count data from exome or targeted sequencing experiments to call copy number variants.

Details

Package:	ExomeDepth
Type:	Package
Version:	0.1
Date:	2012-02-01
License:	What license is it under?
LazyLoad:	yes

The two key functions are: select.reference.set CallCNVs

Author(s)

Vincent Plagnol Maintainer: Vincent Plagnol <[e-mail]>

References

A robust model for read count data in exome sequencing experiments and implications for copy number variant calling, Bioinformatics, In Press

drramki-chop/edm documentation built on June 6, 2020, 8:48 a.m.