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PMID: 24974376 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S.

Prospects for building large timetrees using molecular data with incomplete gene coverage among species.

Molecular biology and evolution ·Vol. 31 ·No. 9 ·2014-09-00 ·Pages 2542-50

Filipski A, Murillo O, Freydenzon A, Tamura K, Kumar S

Abstract

Scientists are assembling sequence data sets from increasing numbers of species and genes to build comprehensive timetrees. However, data are often unavailable for some species and gene combinations, and the proportion of missing data is often large for data sets containing many genes and species. Surprisingly, there has not been a systematic analysis of the effect of the degree of sparseness of the species-gene matrix on the accuracy of divergence time estimates. Here, we present results from computer simulations and empirical data analyses to quantify the impact of missing gene data on divergence time estimation in large phylogenies. We found that estimates of divergence times were robust even when sequences from a majority of genes for most of the species were absent. From the analysis of such extremely sparse data sets, we found that the most egregious errors occurred for nodes in the tree that had no common genes for any pair of species in the immediate descendant clades of the node in question. These problematic nodes can be easily detected prior to computational analyses based only on the input sequence alignment and the tree topology. We conclude that it is best to use larger alignments, because adding both genes and species to the alignment augments the number of genes available for estimating divergence events deep in the tree and improves their time estimates.

Keywords
divergence time incomplete data timetree
MeSH Terms
Computer Simulation Evolution, Molecular Genes Models, Genetic Phylogeny Sequence Alignment/methods Sequence Analysis, DNA
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Filipski Alan
Center for Evolutionary Medicine and Informatics, Biodesign Institute, Arizona State University.
Murillo Oscar
Center for Evolutionary Medicine and Informatics, Biodesign Institute, Arizona State UniversitySchool of Life Sciences, Arizona State University.
Freydenzon Anna
Center for Evolutionary Medicine and Informatics, Biodesign Institute, Arizona State University.
Tamura Koichiro
Department of Biological Sciences, Tokyo Metropolitan University, Tokyo, JapanResearch Center for Genomics and Bioinformatics, Tokyo Metropolitan University, Tokyo, Japan.
Kumar Sudhir
Center for Evolutionary Medicine and Informatics, Biodesign Institute, Arizona State UniversitySchool of Life Sciences, Arizona State UniversityCenter of Excellence in Genomic Medicine Research, King Abdulaziz University, Jeddah, Saudi ArabiaInstitute for Genomics and Evolutionary Medicine, Temple UniversityDepartment of Biology, Temple University s.kumar@temple.edu.
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Article Info
Journal
Molecular biology and evolution
Abbr.
Mol Biol Evol
ISSN
1537-1719
Published
2014-09-00
Epub
2014-00-27
Pages
2542-50
Language
English
Region
United States
NLM ID
8501455
PMCID
PMC4137717
Subset
IM
Grants
NHGRI NIH HHS · R21 HG006039 · United States
NHGRI NIH HHS · R01 HG002096 · United States
NHGRI NIH HHS · HG002096-12 · United States
NHGRI NIH HHS · HG006039-02 · United States
NIGMS NIH HHS · R25 GM099650 · United States
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