CoNVaDING

Copy Number Variation Detection In Next-generation sequencing Gene panels was designed for small (single-exon) copy number variation (CNV) detection in high coverage next-generation sequencing (NGS) data

The documentation for version 1.2.0 can be found here:

https://molgenis.gitbook.io/convading/

For documentation on version 1.1.6 please refer to:

http://molgenis.github.io/CoNVaDING/