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Update: README.md

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@@ -3,9 +3,14 @@ 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`.
You need to manually set the caller to `true` in the submitted sample.csv.

**Germline**
* Haplotyper

If you only want to call germline variants, please set `germline` to true.

**Somatic**
* TNseq (TNhaplotyper2)
* TNscope

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