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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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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.] |
format | Online Article Text |
id | pubmed-7302051 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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