The DOI matches its Crossref record; 21 of the 21 references it cites were found in a registry or an index.
A space-time process model for the evolution of DNA sequences.
Abstract
We describe a model for the evolution of DNA sequences by nucleotide substitution, whereby nucleotide sites in the sequence evolve over time, whereas the rates of substitution are variable and correlated over sites. The temporal process used to describe substitutions between nucleotides is a continuous-time Markov process, with the four nucleotides as the states. The spatial process used to describe variation and dependence of substitution rates over sites is based on a serially correlated gamma distribution, i.e., an auto-gamma model assuming Markov-dependence of rates at adjacent sites. To achieve computational efficiency, we use several equal-probability categories to approximate the gamma distribution, and the result is an auto-discrete-gamma model for rates over sites. Correlation of rates at sites then is modeled by the Markov chain transition of rates at adjacent sites from one rate category to another, the states of the chain being the rate categories. Two versions of nonparametric models, which place no restrictions on the distributional forms of rates for sites, also are considered, assuming either independence or Markov dependence. The models are applied to data of a segment of mitochondrial genome from nine primate species. Model parameters are estimated by the maximum likelihood method, and models are compared by the likelihood ratio test. Tremendous variation of rates among sites in the sequence is revealed by the analyses, and when rate differences for different codon positions are appropriately accounted for in the models, substitution rates at adjacent sites are found to be strongly (positively) correlated. Robustness of the results to uncertainty of the phylogenetic tree linking the species is examined.
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Citations
Cites
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Self-citationMitochondrial DNA sequences of primates: tempo and mode of evolution
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Mutation rates differ among regions of the mammalian genome
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Kalyaanamoorthy, S., Minh, B. Q., Wong, T. K. F., von Haeseler, A., & Jermiin, L. S. (2017) · Nature Methods · doi:10.1038/nmeth.4285 · Cited by 18,449
PAML 4: Phylogenetic Analysis by Maximum Likelihood
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Self-citationEvolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes
Siepel, A., Bejerano, G., Pedersen, J. S., Hinrichs, A. S., Hou, M., Rosenbloom, K., Clawson, H., Spieth, J., Hillier, L. W., Richards, S., et al. (2005) · Genome Research · doi:10.1101/gr.3715005 · Cited by 3,971
ModelTest-NG: A New and Scalable Tool for the Selection of DNA and Protein Evolutionary Models
Darriba, D., Posada, D., Kozlov, A. M., Stamatakis, A., Morel, B., & Flouri, T. (2020) · Molecular Biology and Evolution · doi:10.1093/molbev/msz189 · Cited by 2,105
A Bayesian Mixture Model for Across-Site Heterogeneities in the Amino-Acid Replacement Process
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Metadata
- Authors
- Yang, Z.
- Venue
- Genetics
- Publisher
- Oxford University Press (OUP)
- Published
- 1995-02-01
- Volume
- 139
- Issue
- 2
- Pages
- 993-1005
- ISSN
- 0016-6731 (ISSN-L)
- 1943-2631
- OpenAlex
- W1957469265
- Cited by
- 428
- References
- 21
- FWCI
- 2.25
- Type
- journal article
- Language
- en
- Open access
- closed
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.