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
Oct 7, 2024 at 08:46
License
GPL-3.0
Total Downloads
822
Supported Platforms
GitHub Repository
https://github.com/PathoGenOmics-Lab/get_mnvDocumentation
https://github.com/PathoGenOmics-Lab/get_mnv