Update: README

README.md

@@ -8,6 +8,8 @@ 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).
 
+* Both <u>**FASTQ and BAM data are acceptable**</u>.
+* Please set the parameter `input_fastq` to `true` when the input is FASTQ, or set the parameter `input_bam` to `true` when the input is BAM.
 
 **Supported variant callers and annotation tools**