get_mnv
Tool to identify Multi-Nucleotide Variants (MNVs) in genomic sequences.
Tool to identify Multi-Nucleotide Variants (MNVs) in genomic sequences.
To install this package, run one of the following:
get_MNV is a tool designed to identify Multi-Nucleotide Variants (MNVs) within the same codon in genomic sequences, providing more accurate annotation for genomic data.
Summary
Tool to identify Multi-Nucleotide Variants (MNVs) in genomic sequences.
Last Updated
Feb 25, 2026 at 22:48
License
GPL-3.0-or-later
Total Downloads
1.0K
Version Downloads
143
Supported Platforms
GitHub Repository
https://github.com/PathoGenOmics-Lab/get_mnvDocumentation
https://github.com/PathoGenOmics-Lab/get_mnv