Update: README

README.md

@@ -1,7 +1,7 @@
 ### Variant Calling
 This APP developed for germline and somatic short variant discovery (SNVs + Indels).
 
->**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
@@ -9,8 +9,9 @@ This APP developed for germline and somatic short variant discovery (SNVs + Inde
 
 The datatype is judged by whether the bed file is set (i.e. the `regions` in inputs).
 
+---
 
->**Supported Callers**
+**Supported Callers**
 
 * The fields corresponding to these callers include `haplotyper`, `tnseq`, `tnscope`, `varscan`.
 * All callers are <u>**not activated by default**</u>, which means the default setting is `false`. 
@@ -24,8 +25,9 @@ The datatype is judged by whether the bed file is set (i.e. the `regions` in inp
 * TNscope
 * VarScan
 
+---
 
->**Annotation Tools**
+**Annotation Tools**
 * The fields corresponding to two tools include `annovar`, `vep`.
 * All tools are <u>**not activated by default**</u>, which means the default setting is `false`. 
 * You need to manually set the caller to `true` in the submitted sample.csv.