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The Implications of Lineage-Specific Rates for Divergence Time Estimation

Rate variation adds considerable complexity to divergence time estimation in molecular phylogenies. Here, we evaluate the impact of lineage-specific rates—which we define as among-branch-rate-variation that acts consistently across the entire genome. We compare its impact to residual rates—defined a...

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Autores principales: Carruthers, Tom, Sanderson, Michael J, Scotland, Robert W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7302051/
https://www.ncbi.nlm.nih.gov/pubmed/31808929
http://dx.doi.org/10.1093/sysbio/syz080
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author Carruthers, Tom
Sanderson, Michael J
Scotland, Robert W
author_facet Carruthers, Tom
Sanderson, Michael J
Scotland, Robert W
author_sort Carruthers, Tom
collection PubMed
description Rate variation adds considerable complexity to divergence time estimation in molecular phylogenies. Here, we evaluate the impact of lineage-specific rates—which we define as among-branch-rate-variation that acts consistently across the entire genome. We compare its impact to residual rates—defined as among-branch-rate-variation that shows a different pattern of rate variation at each sampled locus, and gene-specific rates—defined as variation in the average rate across all branches at each sampled locus. We show that lineage-specific rates lead to erroneous divergence time estimates, regardless of how many loci are sampled. Further, we show that stronger lineage-specific rates lead to increasing error. This contrasts to residual rates and gene-specific rates, where sampling more loci significantly reduces error. If divergence times are inferred in a Bayesian framework, we highlight that error caused by lineage-specific rates significantly reduces the probability that the 95% highest posterior density includes the correct value, and leads to sensitivity to the prior. Use of a more complex rate prior—which has recently been proposed to model rate variation more accurately—does not affect these conclusions. Finally, we show that the scale of lineage-specific rates used in our simulation experiments is comparable to that of an empirical data set for the angiosperm genus Ipomoea. Taken together, our findings demonstrate that lineage-specific rates cause error in divergence time estimates, and that this error is not overcome by analyzing genomic scale multilocus data sets. [Divergence time estimation; error; rate variation.]
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spelling pubmed-73020512020-06-23 The Implications of Lineage-Specific Rates for Divergence Time Estimation Carruthers, Tom Sanderson, Michael J Scotland, Robert W Syst Biol Regular Articles Rate variation adds considerable complexity to divergence time estimation in molecular phylogenies. Here, we evaluate the impact of lineage-specific rates—which we define as among-branch-rate-variation that acts consistently across the entire genome. We compare its impact to residual rates—defined as among-branch-rate-variation that shows a different pattern of rate variation at each sampled locus, and gene-specific rates—defined as variation in the average rate across all branches at each sampled locus. We show that lineage-specific rates lead to erroneous divergence time estimates, regardless of how many loci are sampled. Further, we show that stronger lineage-specific rates lead to increasing error. This contrasts to residual rates and gene-specific rates, where sampling more loci significantly reduces error. If divergence times are inferred in a Bayesian framework, we highlight that error caused by lineage-specific rates significantly reduces the probability that the 95% highest posterior density includes the correct value, and leads to sensitivity to the prior. Use of a more complex rate prior—which has recently been proposed to model rate variation more accurately—does not affect these conclusions. Finally, we show that the scale of lineage-specific rates used in our simulation experiments is comparable to that of an empirical data set for the angiosperm genus Ipomoea. Taken together, our findings demonstrate that lineage-specific rates cause error in divergence time estimates, and that this error is not overcome by analyzing genomic scale multilocus data sets. [Divergence time estimation; error; rate variation.] Oxford University Press 2020-07 2019-12-06 /pmc/articles/PMC7302051/ /pubmed/31808929 http://dx.doi.org/10.1093/sysbio/syz080 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the Society of Systematic Biologists. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Regular Articles
Carruthers, Tom
Sanderson, Michael J
Scotland, Robert W
The Implications of Lineage-Specific Rates for Divergence Time Estimation
title The Implications of Lineage-Specific Rates for Divergence Time Estimation
title_full The Implications of Lineage-Specific Rates for Divergence Time Estimation
title_fullStr The Implications of Lineage-Specific Rates for Divergence Time Estimation
title_full_unstemmed The Implications of Lineage-Specific Rates for Divergence Time Estimation
title_short The Implications of Lineage-Specific Rates for Divergence Time Estimation
title_sort implications of lineage-specific rates for divergence time estimation
topic Regular Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7302051/
https://www.ncbi.nlm.nih.gov/pubmed/31808929
http://dx.doi.org/10.1093/sysbio/syz080
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