Evidence map›Paper›PMID 23188590›Full record

ArticleMolecular biology and evolution2013

Estimating empirical codon hidden Markov models.

Nicola De Maio, Ian Holmes, Christian Schlötterer, Carolin Kosiol

Abstract read
In one paragraph

Article in Molecular biology and evolution, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

15 citing papers in PubMed.

  1. Article
  2. Highly Recurrent Multinucleotide Mutations in SARS-CoV-2.Molecular biology and evolution · 2025
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Gene-wide identification of episodic selection.Molecular biology and evolution · 2015
    Article
  12. A generalized mechanistic codon model.Molecular biology and evolution · 2014
    Article
  13. Article
  14. Article
  15. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Nicola De MaioInstitut für Populationsgenetik, Vetmeduni Vienna, Wien, Austria. nicola.de.maio.85@gmail.com
Ian Holmes
Christian Schlötterer
Carolin Kosiol

Funding

Web-based visualization of coronavirus genomes and proteinsR01HG004483 · NHGRI · UNIVERSITY OF CALIFORNIA BERKELEY · PI Ian H Holmes · 2007 to 2026
$9.3M
Austrian Science Fund FWF P 19467Austrian Science Fund FWF P 24551Austrian Science Fund FWF W 1225NHGRI NIH HHS 2R01HG004483NHGRI NIH HHS R01 HG004483
6 · The paper itself

Abstract

Empirical codon models (ECMs) estimated from a large number of globular protein families outperformed mechanistic codon models in their description of the general process of protein evolution. Among other factors, ECMs implicitly model the influence of amino acid properties and multiple nucleotide substitutions (MNS). However, the estimation of ECMs requires large quantities of data, and until recently, only few suitable data sets were available. Here, we take advantage of several new Drosophila species genomes to estimate codon models from genome-wide data. The availability of large numbers of genomes over varying phylogenetic depths in the Drosophila genus allows us to explore various divergence levels. In consequence, we can use these data to determine the appropriate level of divergence for the estimation of ECMs, avoiding overestimation of MNS rates caused by saturation. To account for variation in evolutionary rates along the genome, we develop new empirical codon hidden Markov models (ecHMMs). These models significantly outperform previous ones with respect to maximum likelihood values, suggesting that they provide a better fit to the evolutionary process. Using ECMs and ecHMMs derived from genome-wide data sets, we devise new likelihood ratio tests (LRTs) of positive selection. We found classical LRTs very sensitive to the presence of MNSs, showing high false-positive rates, especially with small phylogenies. The new LRTs are more conservative than the classical ones, having acceptable false-positive rates and reduced power.

Indexed as

Models, GeneticAlgorithmsAnimalsCodonComputer SimulationDrosophilaEvolution, MolecularGenetic SpeciationGenome, InsectLikelihood FunctionsMarkov ChainsMutation RateOpen Reading FramesPhylogenySelection, GeneticCodon

Identifiers

PMID23188590
PMCPMC3563974

What OpenQuestion holds

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LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.