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Update: README.md

tags/v0.1.2
YaqingLiu 4 年前
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@@ -6,11 +6,13 @@ This APP developed for somatic short variant discovery (SNVs + Indels).
* TNscope
* VarScan
* TNhaplotyper (This caller is only available in `v0.1.0` as it is too outdated)

Variant caller can be selected by setting `ture/false` in the submitted sample.csv.

***Accepted data***
* TN matched WES
* WGS
* TN matched WGS

The datatype is judged by whether the bed file is set (i.e. the `regions` in inputs).

### New Releases

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