Nextflow Modules
Showing module(s) with keyword "Pharmacogenetics"
| Module | Keywords | Description |
|---|---|---|
| nf-core/pypgx/createinputvcf | pypgx Pharmacogenetics variants | Call SNVs/indels from BAM files for all target genes. |
| nf-core/pypgx/preparedepthofcoverage | Pharmacogenetics pypgx SV | Prepare a depth of coverage file for all target genes with SV from BAM files. |