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A simulation study comparing supertree and combined analysis methods using SMIDGen

Authors :
Warnow Tandy
Barbançon François
Swenson M Shel
Linder C Randal
Source :
Algorithms for Molecular Biology, Vol 5, Iss 1, p 8 (2010)
Publication Year :
2010
Publisher :
BMC, 2010.

Abstract

Abstract Background Supertree methods comprise one approach to reconstructing large molecular phylogenies given multi-marker datasets: trees are estimated on each marker and then combined into a tree (the "supertree") on the entire set of taxa. Supertrees can be constructed using various algorithmic techniques, with the most common being matrix representation with parsimony (MRP). When the data allow, the competing approach is a combined analysis (also known as a "supermatrix" or "total evidence" approach) whereby the different sequence data matrices for each of the different subsets of taxa are concatenated into a single supermatrix, and a tree is estimated on that supermatrix. Results In this paper, we describe an extensive simulation study we performed comparing two supertree methods, MRP and weighted MRP, to combined analysis methods on large model trees. A key contribution of this study is our novel simulation methodology (Super-Method Input Data Generator, or SMIDGen) that better reflects biological processes and the practices of systematists than earlier simulations. We show that combined analysis based upon maximum likelihood outperforms MRP and weighted MRP, giving especially big improvements when the largest subtree does not contain most of the taxa. Conclusions This study demonstrates that MRP and weighted MRP produce distinctly less accurate trees than combined analyses for a given base method (maximum parsimony or maximum likelihood). Since there are situations in which combined analyses are not feasible, there is a clear need for better supertree methods. The source tree and combined datasets used in this study can be used to test other supertree and combined analysis methods.

Details

Language :
English
ISSN :
17487188
Volume :
5
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Algorithms for Molecular Biology
Publication Type :
Academic Journal
Accession number :
edsdoj.b5ee02e5c576476cb2b455b60a92e29f
Document Type :
article
Full Text :
https://doi.org/10.1186/1748-7188-5-8