diff --git a/README.md b/README.md index c2525b0b..53ebc165 100644 --- a/README.md +++ b/README.md @@ -5,10 +5,8 @@ tests](https://github.com/WGLab/ContextSV/actions/workflows/build-tests.yml/badg ![contextsv_small_15p](https://github.com/WGLab/ContextSV/assets/14855676/79d70c76-a34a-472e-a14c-e49489ae0f09) # ContextSV -_This is a work in progress, software is under development and not ready for official release._ -An alignment-based, generalized structural variant caller for long-read -sequencing/mapping data. +Whole-genome structural variant caller for long read sequencing data. ContextSV takes as input a long read alignments file (BAM), a corresponding reference genome file (FASTA), a VCF file with high-quality SNPs