diff --git a/README.md b/README.md index 305008c..222eb9f 100644 --- a/README.md +++ b/README.md @@ -84,8 +84,6 @@ You need to either provide the length of your reference genome or if you want to Additionally, you can also analyse if mutations are sufficiently covered and display non-covered cells in grey. For that first create a per base coverage tsv files for each bam file with [Qualimap](http://qualimap.conesalab.org/) and provide it in the same folder as the vcf files. Give them the same name as your vcf files. -Buy Me A Coffee - --- **Important disclaimer:**