Update: README.md

README.md

@@ -6,11 +6,13 @@ This APP developed for somatic short variant discovery (SNVs + Indels).
 * TNscope
 * VarScan
 * TNhaplotyper (This caller is only available in `v0.1.0` as it is too outdated)
+
 Variant caller can be selected by setting `ture/false` in the submitted sample.csv.
 
 ***Accepted data***
 * TN matched WES
-* WGS
+* TN matched WGS
+
 The datatype is judged by whether the bed file is set (i.e. the `regions` in inputs).
 
 ### New Releases