Evidence map›Paper›PMID 32119075›Full record

ArticleMolecular biology and evolution2020

Relative Efficiencies of Simple and Complex Substitution Models in Estimating Divergence Times in Phylogenomics.

Qiqing Tao, Jose Barba-Montoya, Louise A Huuki, Mary Kathleen Durnan, Sudhir Kumar

Abstract readEvaluation Study
In one paragraph

Article in Molecular biology and evolution, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

14 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Challenges in Assembling the Dated Tree of Life.Genome biology and evolution · 2024
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Methodologies for Microbial Ancestral Sequence Reconstruction.Methods in molecular biology (Clifton, N.J.) · 2022
    Review
  13. Article
  14. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Qiqing TaoInstitute for Genomics and Evolutionary Medicine, Temple University, Philadelphia, PA.
Jose Barba-MontoyaInstitute for Genomics and Evolutionary Medicine, Temple University, Philadelphia, PA.
Louise A HuukiInstitute for Genomics and Evolutionary Medicine, Temple University, Philadelphia, PA.
Mary Kathleen DurnanInstitute for Genomics and Evolutionary Medicine, Temple University, Philadelphia, PA.
Sudhir KumarInstitute for Genomics and Evolutionary Medicine, Temple University, Philadelphia, PA.

Funding

Inferring molecular evolutionary rates and divergence datesR01GM126567 · NIGMS · TEMPLE UNIV OF THE COMMONWEALTH · PI KUMAR, SUDHIR · 2018 to 2020
$951k
NIGMS NIH HHS R01 GM126567
6 · The paper itself

Abstract

The conventional wisdom in molecular evolution is to apply parameter-rich models of nucleotide and amino acid substitutions for estimating divergence times. However, the actual extent of the difference between time estimates produced by highly complex models compared with those from simple models is yet to be quantified for contemporary data sets that frequently contain sequences from many species and genes. In a reanalysis of many large multispecies alignments from diverse groups of taxa, we found that the use of the simplest models can produce divergence time estimates and credibility intervals similar to those obtained from the complex models applied in the original studies. This result is surprising because the use of simple models underestimates sequence divergence for all the data sets analyzed. We found three fundamental reasons for the observed robustness of time estimates to model complexity in many practical data sets. First, the estimates of branch lengths and node-to-tip distances under the simplest model show an approximately linear relationship with those produced by using the most complex models applied on data sets with many sequences. Second, relaxed clock methods automatically adjust rates on branches that experience considerable underestimation of sequence divergences, resulting in time estimates that are similar to those from complex models. And, third, the inclusion of even a few good calibrations in an analysis can reduce the difference in time estimates from simple and complex models. The robustness of time estimates to model complexity in these empirical data analyses is encouraging, because all phylogenomics studies use statistical models that are oversimplified descriptions of actual evolutionary substitution processes.

Indexed as

Evolution, MolecularModels, GeneticPhylogenyGenomicsPlantsmolecular datingphylogenomicsrelaxed clockRelTimesubstitution model

Identifiers

PMID32119075
PMCPMC7253201

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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.