Update: README.md

README.md

@@ -1,6 +1,6 @@
+### Variant calling
 This APP developed for somatic short variant discovery (SNVs + Indels).
 
-
 ***Supported callers***
 * TNhaplotyper2
 * TNscope
@@ -14,11 +14,11 @@ Variant caller can be selected by setting `ture/false` in the submitted sample.c
 The datatype is judged by whether the bed file is set (i.e. the `regions` in inputs).
 
 
-#### New version
+### New version
 * The TNhaplotyper, also named as TNseq in `v0.1.0`, has beed substituted by TNhaplotyper2.
 * The `corealigner` step has been removed.
 
-#### How to run this APP
+### How to run this APP
 
 We recommend using choppy system and Aliyun OSS service. The command will look like this: