Update: README.md

README.md

@@ -7,10 +7,10 @@ This APP developed for germline and somatic short variant discovery (SNVs + Inde
 * 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***
+<u>***Germline***</u>
 * Haplotyper
 
-***Somatic***
+<u>***Somatic***</u>
 * TNseq (TNhaplotyper2)
 * TNscope
 * VarScan