Update: README.md

README.md

@@ -1,17 +1,19 @@
 This APP developed for somatic short variant discovery (SNVs + Indels).
 
-**Supported callers**
+
+***Supported callers***
 * TNhaplotyper2
 * 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 * TNhaplotyper (This caller is only available in `v0.1.0` as it is too outdated)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.
 
-**Types of data that can be received**
+***Accepted data***
 * TN matched WES
 * WGS
 The datatype is judged by whether the bed file is set (i.e. the `regions` in inputs).
 
+
 #### New version
 * The TNhaplotyper, also named as TNseq in `v0.1.0`, has beed substituted by TNhaplotyper2.
 * The `corealigner` step has been removed.