To understand the patterns and processes underlying the evolutionary dynamics of multigene families, genomes, and model organisms and their close relatives, it is crucial to to develop easy-to-use computer tools for comparative sequence analysis. The investigator proposes to develop Molecular Evolutionary Genetic Analysis 2 (MEGA2) for examining sequences from different perspectives. MEGA2 will support analysis of (1) sequence and polymorphism data, as well as restriction site, allele frequency, and microsatellite data; (2) allow specifications of domains and genes (collections of domains) for comparative analysis; (3) allow for creation of groups of sequences for multigene family and higher level phylogenetic analysis; (4) establish new graphics standards for data representation; (5) provide intuitive sequence alignment construction with emphasis on alignment to genomic sequences; (6) implement existing and develop new computational and statistical methods for sequence data in an easy-to-use, consistent framework. MEGA2 will include programs for estimating evolutionary distances, computing genetic diversity within and among groups of sequences, inferring and testing evolutionary trees, conducting molecular clock tests, inferring ancestral molecular sequences, and testing a variety of evolutionary hypotheses by the bootstrap technique, among other statistical methods.

Agency
National Institute of Health (NIH)
Institute
National Human Genome Research Institute (NHGRI)
Type
Research Project (R01)
Project #
5R01HG002096-03
Application #
6490441
Study Section
Genome Study Section (GNM)
Program Officer
Brooks, Lisa
Project Start
2000-01-01
Project End
2003-03-31
Budget Start
2002-01-01
Budget End
2003-03-31
Support Year
3
Fiscal Year
2002
Total Cost
$241,455
Indirect Cost
Name
Arizona State University-Tempe Campus
Department
Other Basic Sciences
Type
Schools of Arts and Sciences
DUNS #
188435911
City
Tempe
State
AZ
Country
United States
Zip Code
85287
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Liu, Li; Tamura, Koichiro; Sanderford, Maxwell et al. (2016) A Molecular Evolutionary Reference for the Human Variome. Mol Biol Evol 33:245-54
Miura, Sayaka; Tate, Stephanie; Kumar, Sudhir (2015) Using Disease-Associated Coding Sequence Variation to Investigate Functional Compensation by Human Paralogous Proteins. Evol Bioinform Online 11:245-51
Kumar, Avishek; Butler, Brandon M; Kumar, Sudhir et al. (2015) Integration of structural dynamics and molecular evolution via protein interaction networks: a new era in genomic medicine. Curr Opin Struct Biol 35:135-42
Butler, Brandon M; Gerek, Z Nevin; Kumar, Sudhir et al. (2015) Conformational dynamics of nonsynonymous variants at protein interfaces reveals disease association. Proteins 83:428-35
Filipski, Alan; Tamura, Koichiro; Billing-Ross, Paul et al. (2015) Phylogenetic placement of metagenomic reads using the minimum evolution principle. BMC Genomics 16 Suppl 1:S13
Battistuzzi, Fabia U; Billing-Ross, Paul; Murillo, Oscar et al. (2015) A Protocol for Diagnosing the Effect of Calibration Priors on Posterior Time Estimates: A Case Study for the Cambrian Explosion of Animal Phyla. Mol Biol Evol 32:1907-12
Gerek, Nevin Z; Liu, Li; Gerold, Kristyn et al. (2015) Evolutionary Diagnosis of non-synonymous variants involved in differential drug response. BMC Med Genomics 8 Suppl 1:S6
Hedges, S Blair; Marin, Julie; Suleski, Michael et al. (2015) Tree of life reveals clock-like speciation and diversification. Mol Biol Evol 32:835-45

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