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.
Basic Information
| Repository | https://github.com/PathoGenOmics-Lab/get_MNV |
| Documentation | https://github.com/PathoGenOmics-Lab/get_MNV/blob/main/README.md |
| Main publication (DOI) | 10.5281/zenodo.13907422 view |
| Contact email | paula.ruiz.rodriguez@csic.es |
| Authors/Maintainers | Mireia Coscolla Devis, Paula Ruiz Rodríguez |
| Type of application | Command line pipeline, Conda package |
| Programming languages | Rust |
| Keywords | Omics, Resources, Bioinformatics Software and Tools, Annotation tools, Genomics, Genomic Annotation |
Technical details
| Input file formats | |
| Output file formats | |
| Software compatibility | Linux, Mac |
| Hardware requirements | No specific hardware requirements |
| Type of containerization | None |
| Wrapper type | None |
| Compatible tools | |
| Funding resource | No funding |
| Funding support | No funding |
Statistics
| Unique users (last 12 months) | |
| Unique users (since first release) | |
| Software downloads (last 12 months) | 640 |
| Software downloads (since first release) | 640 |
| Jobs submitted (last 12 months) | |
| Jobs submitted (since first release) | |
| Repository clones (last 12 months) | |
| Repository clones (since first release) | |
| Citations (last 12 months) | <100 (~0 as of 15/10/2026) |
| Citations (since first release) | <100 (0 as of 15/10/2026) |
| Early-stage researcher effort (development) | doctoral candidate |
| Early-stage researcher effort (maintenance) | doctoral candidate |
| Technician-supported effort (development) | |
| Technician-supported effort (maintenance) | |
| Other effort (development) | |
| Other effort (maintenance) | |
| Total effort (development) | |
| Total effort (maintenance) |