Nextflow Modules
Showing module(s) with keyword "cancer genome"
| Module | Keywords | Description |
|---|---|---|
| nf-core/nanomonsv/parse | structural variants nanopore cancer genome somatic structural variations mobile element insertions long reads | Parse all the supporting reads of putative somatic SVs using nanomonsv. After successful completion, you will find supporting reads stratified by deletions, insertions, and rearrangements. A precursor to "nanomonsv get" |