Update: README.md

README.md

@@ -1,24 +1,22 @@
 ### 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`. 
+* 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.
+* The fields corresponding to these callers include `haplotyper`, `tnseq`, `tnscope`, `varscan`.
 
-You need to manually set the caller to `true` in the submitted sample.csv.
-
-The fields corresponding to these callers include `haplotyper`, `tnseq`, `tnscope`, `varscan`.
-
-**Germline**
+***Germline***
 * Haplotyper
 
-**Somatic**
+***Somatic***
 * TNseq (TNhaplotyper2)
 * TNscope
 * 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 * TNhaplotyper (This caller is only available in `v0.1.0` as it is too outdated)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