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Update: README.md

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@@ -3,7 +3,7 @@ This APP developed for germline and somatic short variant discovery (SNVs + Inde

**Supported Callers**

* All callers are **not activated by default**, which means the default setting is `false`.
* All callers 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.
* The fields corresponding to these callers include `haplotyper`, `tnseq`, `tnscope`, `varscan`.


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