get_MNV

get_MNV is a tool designed to identify Multi-Nucleotide Variants (MNVs) within the same codon in genomic sequences. MNVs occur when multiple Single Nucleotide Variants (SNVs) are present within the same codon, leading to the translation of a different amino acid.

Info

Members (researchers): Paula Ruiz Rodríguez, Mireia Coscolla

Research Groups: PathoGenOmics

Contact Email: paula.ruiz.rodriguez@csic.es

Tool Repository: https://github.com/PathoGenOmics-Lab/get_MNV

Documentation: https://github.com/PathoGenOmics-Lab/get_MNV/blob/main/README.md

Institution: Instituto de Biología Integrativa de Sistemas (I2SYSBIO)

Application domain:

Annotation tools, Genomic Annotation, Genomics

Technical details
Type of application
  • Command line pipeline
  • Conda package
Software compatibility
  • Linux
  • Mac
Hardware requirements
  • No specific hardware requirements
Programming language
  • Rust
Type of containerization
  • None
Wrapper type
  • None
Input file formats
Output file formats
Compatibility with other tools