diff --git a/README.md b/README.md index f2fed477..220d61aa 100644 --- a/README.md +++ b/README.md @@ -1,5 +1,4 @@ - -
+# Nirvana Nirvana provides **clinical-grade annotation of genomic variants** (SNVs, MNVs, insertions, deletions, indels, and SVs (including CNVs). It can be run as a stand-alone package or integrated into larger software tools that require variant annotation. @@ -12,6 +11,5 @@ Backronym: **NI**mble and **R**obust **VA**riant a**N**not**A**tor ## Resources -* [Getting Started](https://github.com/Illumina/Nirvana/wiki/Getting-Started) -* [Wiki](https://github.com/Illumina/Nirvana/wiki) +* [Documentation](https://illumina.github.io/NirvanaDocumentation/) * [Release Notes](https://github.com/Illumina/Nirvana/releases)