MAVID
MAVID is a multiple sequence alignment program suitable for the alignment of large numbers of DNA sequences.[1][2] The sequences can be small mitochondrial genomes or large genomic regions up to megabases long. The latest version is 2.0.4.
| Developer(s) | Nicolas Bray (UC Berkeley), Lior Pachter (UC Berkeley) |
|---|---|
| Stable release | 2.0.4
|
| Operating system | UNIX, Linux, Mac |
| Type | Bioinformatics tool |
| Licence | Open source |
| Website | MAVID download |
The program can be used through the MAVID web server or as a standalone program which can be installed with the source code.
Input/Output
This program accepts sequences in FASTA format.
The output format includes: FASTA format, Clustal, PHYLIP.
References
- Dewey, Colin N. (2007), "Aligning Multiple Whole Genomes with Mercator and MAVID", in Bergman, Nicholas H. (ed.), Comparative Genomics, Methods in Molecular Biology, 395, Humana Press, pp. 221–235, doi:10.1007/978-1-59745-514-5_14, ISBN 978-1-58829-693-1, PMID 17993677
- Bray, Nicolas; Pachter, Lior (2003-07-01). "MAVID multiple alignment server". Nucleic Acids Research. 31 (13): 3525–3526. doi:10.1093/nar/gkg623. ISSN 0305-1048. PMC 169029. PMID 12824358.
- Bray, N.; Pachter, L. (2004), "MAVID: Constrained ancestral alignment of multiple sequences", Genome Research, 14 (4): 693–699, arXiv:q-bio/0311018, doi:10.1101/gr.1960404, PMC 383315, PMID 15060012.
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