Update: README

README.md

@@ -13,9 +13,7 @@ The datatype is judged by whether the bed file is set (i.e. the `regions` in inp
 
 **Supported variant callers and annotation tools**
 
-* Variant calling: 
-- `haplotyper` (germline)
-- `tnseq`, `tnscope`, `varscan` (somatic)
+* Variant calling: `haplotyper` (germline); `tnseq`, `tnscope`, `varscan` (somatic).
 * Annotation: `annovar`, `vep`.
 * The above 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.
 
@@ -57,4 +55,4 @@ The parameters that must need contains: sample_id,normal_fastq_1,normal_fastq_2,
 * the caller you want to use.
 * PoN VCFs for TNseq and TNscope is supported, but are need to be generated in advance.
 * interval padding is default 0, and you can change it.
-* the annotation tool is ANNOVAR or VEP.
+* usually only one annotation tool is sufficient.