Evidence map›Paper›PMID 23595859›Full record

ArticleJournal of molecular evolution2013

The site-wise log-likelihood score is a good predictor of genes under positive selection.

Huai-Chun Wang, Edward Susko, Andrew J Roger

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Article in Journal of molecular evolution, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Huai-Chun WangDepartment of Mathematics and Statistics, Dalhousie University, Halifax, NS, B3H 4R2, Canada. hcwang@mathstat.dal.ca
Edward Susko
Andrew J Roger

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The strength and direction of selection on the identity of an amino acid residue in a protein is typically measured by the ratio of the rate of non-synonymous substitutions to the rate of synonymous substitutions. In attempting to predict positively selected sites from amino acid alignments, we made the unexpected observation that the site likelihood of an alignment column for a given tree tends to be negatively correlated with the posterior probability that site is in the positive selection class under widely-used codon models. This is likely because positively selected sites tend to be more variable and display more "radical" amino acid changes; both of these features are expected to result in low site log-likelihoods. We explored the efficacy of using the site log-likelihood (SLL) score as a predictor for positive selection. Through simulation we show that a SLL-based test has a low false positive rate and comparable power as the codon models. In one case where the simulated data violated the assumption that synonymous substitution rates were constant across the sites, the codon models were not able to detect positive selection in the data while the SLL test did. We applied the new method to ten empirical datasets and found that it made similar predictions as the codon models in eight of them. For the tax gene dataset the SLL test seemed to produce more reasonable results. The SLL methods are a valuable complement to codon models, especially for some cases where the assumptions of codon models are likely violated.

Indexed as

CodonModels, GeneticSelection, GeneticAlcohol DehydrogenaseAmino AcidsAmino Acid Substitutionbeta-GlobinsComputer SimulationDrosophila ProteinsEncephalitis Virus, JapaneseEvolution, MolecularFlavivirusHIVLikelihood FunctionsPhylogenyViral ProteinsAlcohol DehydrogenaseAmino Acidsbeta-GlobinsCodonDrosophila ProteinsViral Proteins

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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.