MEGA, Molecular Evolutionary Genetics Analysis

Molecular Evolutionary Genetics Analysis
White sans-serif capital letters spelling MEGA, each in a separate square, colored one red and three black, respectively.
Version 7 (2016)
Original author(s) Masatoshi Nei, Sudhir Kumar, Koichiro Tamura, Glen Stecher, Daniel Peterson, Nicholas Peterson
Developer(s) Pennsylvania State University
Initial release 1993 (1993)
Stable release
10.0.4 / June 2018 (2018-06)
Operating system Windows, OS X, Linux
Platform x86, x86-64
Available in English
Type Bioinformatics
License Proprietary freeware
Website www.megasoftware.net

Molecular Evolutionary Genetics Analysis (MEGA) is computer software for conducting statistical analysis of molecular evolution and for constructing phylogenetic trees. It includes many sophisticated methods and tools for phylogenomics and phylomedicine. It is licensed as proprietary freeware. The project for developing this software was initiated by the leadership of Masatoshi Nei in his laboratory at the Pennsylvania State University in collaboration with his graduate student Sudhir Kumar and postdoctoral fellow Koichiro Tamura.[1] Nei wrote a monograph (pp. 130) outlining the scope of the software and presenting new statistical methods that were included in MEGA. The entire set of computer programs was written by Kumar and Tamura. The personal computers then lacked the ability to send the monograph and software electronically, so they were delivered by postal mail. From the start, MEGA was intended to be easy-to-use and include solid statistical methods only.

MEGA version 2 (MEGA2), which was coauthored by an additional investigator Ingrid Jakobson, was released in 2001.[2] All the computer programs and the readme files of this version could be sent electronically due to advances in computer technology. Around this time, the leadership of the MEGA project was taken over by Kumar (now at Temple University) and Tamura (now at Tokyo Metropolitan University). The monograph Molecular Evolutionary Genetics Analysis was often used as a textbook for new ways to study molecular evolution.

MEGA has been updated and expanded several times and currently all these versions are available from the MEGA website. The latest release, MEGA7, has been optimized for use on 64-bit computing systems. MEGA is in two version. A graphical user interface is available as a native Microsoft Windows program. A command line version, MEGA-Computing Core (MEGA-CC), is available for native cross-platform operation. The method is widely used and cited. With millions of downloads across the releases, MEGA is cited in more than 85,000 papers. The 5th version has been cited over 25,000 times in 4 years.[3]

Release history

Major MEGA versions[4]
Version Release date
1.0 1993[1]
1.1 1994[5]
2.0 2000[2]
2.1 2001[2]
3.0 2004[6]
4.0 2006[7]
4.1 2008[7]
5.0 2011[8]
5.1 Oct 2012[8]
5.2 April 2013[8]
6.0 December 2013[3]
7.0 January 2016[9]
10.0 (X) May 2018[10]

Features

Sequence alignment construction

Data handling

  • Handling ambiguous states: R, Y, T, etc.
  • Extended MEGA format to save all data attributes
  • Importing data from other formats: Clustal, Nexus, etc.
  • Data explorers
  • Visual specification of domains-groups

Genetic code table section

  • Add-edit user defined tables
  • Compute statistical attributes of a code table
  • Include all known code tables

Real-time caption expert engine

  • Generate captions for distance matrices, phylogenies, tests, alignments
  • Copy captions to external programs

Integrated text file editor

  • Columnar block selection-editing
  • Line numbers
  • Utilities to format sequences, reverse complement etc.

Sequence data viewer

  • Data export
  • Highlighting
  • Statistical quantities estimation

MCL-based estimation of nucleotide substitution patterns

  • 4x4 rate matrix
  • Transition-transversion rate ratios: k1, k2
  • Transition-transversion rate bias: R

Substitution pattern homogeneity test

  • Composition distance
  • Disparity index
  • Monte-carlo test

Distance estimation methods

  • Nucleotide-by-nucleotide
  • Synonymous-nonsynonymous: codon-by-codon
  • Protein distance
  • Distance calculations
  • Sequence diversity calculations
  • Variance calculations

Tests of selection

  • Large sample Z-test
  • Fisher’s exact test
  • Tajima’s neutrality test

Molecular clock test

  • Tajima’s relative rate test

Tree-making methods

Tree explorers

  • Phylogeny display
  • Divergence time estimation
  • Tree editing
  • Change tree size
  • Multiple tree display

References

  1. 1 2 Kumar, S., K. Tamura, and M. Nei (1993) MEGA: Molecular Evolutionary Genetics Analysis. Ver. 1.0, The Pennsylvania State University, University Park, PA.
  2. 1 2 3 Kumar, S., K. Tamura, I. B. Jakobsen, and M. Nei (2001) MEGA2: Molecular Evolutionary Genetics Analysis. Ver. 2.0, Bioinformatics 17:1244-1245.
  3. 1 2 Tamura, K., Stecher, G., Peterson, D., Filipski, A., Kumar, S. (2013) MEGA6: Molecular Evolutionary Genetics Analysis Version 6.0. Mol. Biol. Evol. 30:2725-2729.
  4. "MEGA Update History". MEGA: Molecular Evolutionary Genetics Analysis. Retrieved 20 June 2013.
  5. Kumar, S., K. Tamura, and M. Nei (1994) MEGA: Molecular Evolutionary Genetics Analysis software for microcomputers. CABIOS 10:189-191.
  6. Kumar, S., Tamura, K., and Nei, M. (2004) MEGA3: Molecular Evolutionary Genetics Analysis. Brief. Bioinformatics 5:150-163.
  7. 1 2 Tamura, K., Dudley, J., Nei, M., Kumar, S. (2007) MEGA4: Molecular Evolutionary Genetics Analysis. Mol. Biol. Evol. 24(8):1596-1599.
  8. 1 2 3 Tamura, K., Peterson, D., Peterson, N., Stecher, G., Nei, M., Kumar, S. (2011) MEGA5: Molecular Evolutionary Genetics Analysis using Maximum Likelihood, Evolutionary Distance, and Maximum Parsimony Methods. Mol. Biol. Evol. 28:2731-2739.
  9. Kumar, S., Stecher, G., & Tamura, K. (2016). MEGA7: Molecular Evolutionary Genetics Analysis version 7.0 for bigger datasets. Mol. Biol. Evol. 33(7):1870–1874.
  10. Kumar, S., Stecher, G., Li M., Knyaz C. & Tamura, K. (2018). MEGA X: Molecular Evolutionary Genetics Analysis across computing platforms. Mol. Biol. Evol. 35(6):1547-1549.
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