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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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