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README.md
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| @@ -7,10 +7,10 @@ This APP developed for germline and somatic short variant discovery (SNVs + Inde | |||
| * 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`. | |||
| ***Germline*** | |||
| <u>***Germline***</u> | |||
| * Haplotyper | |||
| ***Somatic*** | |||
| <u>***Somatic***</u> | |||
| * TNseq (TNhaplotyper2) | |||
| * TNscope | |||
| * VarScan | |||
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