Description

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"

Input

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Output

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Tools

nanomonsv Documentation

nanomonsv is a software for detecting somatic structural variations from paired (tumor and matched control) cancer genome sequence data.

https://github.com/friend1ws/nanomonsvdoi: 10.1101/2020.07.22.214262 License: GPL v3
Authors