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README.md
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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| * TNhaplotyper (This caller is only available in `v0.1.0` as it is too outdated) | |||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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