Evidence map›Paper›PMID 20093431›Full record

ArticleMolecular biology and evolution2010

Performance of relaxed-clock methods in estimating evolutionary divergence times and their credibility intervals.

Fabia U Battistuzzi, Alan Filipski, S Blair Hedges, Sudhir Kumar

Open access · bronzeAbstract read
In one paragraph

Article in Molecular biology and evolution, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
5.1field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 96 citations in OpenAlex.

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  14. Advances in Time Estimation Methods for Molecular Data.Molecular biology and evolution · 2016
    Article
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  16. Molecular clocks and the early evolution of metazoan nervous systems.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2015
    Review
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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 at 2 institutions in 1 country.

Fabia U BattistuzziCenter for Evolutionary Functional Genomics, The Biodesign Institute, Arizona State University, USA.
Alan Filipski
S Blair Hedges
Sudhir Kumar
Evolutionary Genomics (United States) · USPennsylvania State University · US

Funding

COMPARATIVE MOLECULAR SEQUENCE ANALYSISR01HG002096 · NHGRI · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI KUMAR, SUDHIR · 2000 to 2013
$3.0M
Evolution of Plasmodium vivax and Asian Macaque MalariasR01GM080586 · NIGMS · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI ESCALANTE, ANANIAS ALBERTO · 2008 to 2011
$1.2M
NHGRI NIH HHS HG002096NHGRI NIH HHS R01 HG002096NIGMS NIH HHS GM080586NIGMS NIH HHS R01 GM080586
6 · The paper itself

Abstract

The rapid expansion of sequence data and the development of statistical approaches that embrace varying evolutionary rates among lineages have encouraged many more investigators to use DNA and protein data to time species divergences. Here, we report results from a systematic evaluation, by means of computer simulation, of the performance of two frequently used relaxed-clock methods for estimating these times and their credibility intervals (CrIs). These relaxed-clock methods allow rates to vary in a phylogeny randomly over lineages (e.g., BEAST software) and in autocorrelated fashion (e.g., MultiDivTime software). We applied these methods for analyzing sequence data sets simulated using naturally derived parameters (evolutionary rates, sequence lengths, and base substitution patterns) and assuming that clock calibrations are known without error. We find that the estimated times are, on average, close to the true times as long as the assumed model of lineage rate changes matches the actual model. The 95% CrIs also contain the true time for >or=95% of the simulated data sets. However, the use of incorrect lineage rate model reduces this frequency to 83%, indicating that the relaxed-clock methods are not robust to the violation of underlying lineage rate model. Because these rate models are rarely known a priori and are difficult to detect empirically, we suggest building composite CrIs using CrIs produced from MultiDivTime and BEAST analysis. These composite CrIs are found to contain the true time for >or=97% data sets. Our analyses also verify the usefulness of the common practice of interpreting the congruence of times inferred from different methods as a reflection of the accuracy of time estimates. Overall, our results show that simple strategies can be used to enhance our ability to estimate times and their CrIs when using the relaxed-clock methods.

Indexed as

Databases, GeneticEvolution, MolecularModels, StatisticalPhylogenyAnimalsBase CompositionComputational BiologyComputer SimulationMammalsModels, GeneticSequence AlignmentSoftware

Identifiers

PMID20093431
PMCPMC2877995
OpenAlexW2110522871

What OpenQuestion holds

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Registered trials

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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.