Update: README.md

README.md

@@ -1,7 +1,7 @@
 ### Variant Calling
 This APP developed for germline and somatic short variant discovery (SNVs + Indels).
 
-**Supported callers**
+**Supported Callers**
 
 * All callers are **not activated by default**, which means the default setting is `false`. 
 * You need to manually set the caller to `true` in the submitted sample.csv.
@@ -16,7 +16,7 @@ This APP developed for germline and somatic short variant discovery (SNVs + Inde
 * VarScan
 * TNhaplotyper (This caller is only available in `v0.1.0` as it is too outdated)
 
-**Accepted data**
+**Accepted Data**
 * TN matched WES for somatic variant calling
 * TN matched WGS for somatic variant calling
 * Normal-only WES for germline variant calling