Literature DB >> 11110896

Reconstructing genealogies of serial samples under the assumption of a molecular clock using serial-sample UPGMA.

A Drummond1, A G Rodrigo.   

Abstract

Reconstruction of evolutionary relationships from noncontemporaneous molecular samples provides a new challenge for phylogenetic reconstruction methods. With recent biotechnological advances there has been an increase in molecular sequencing throughput, and the potential to obtain serial samples of sequences from populations, including rapidly evolving pathogens, is fast being realized. A new method called the serial-sample unweighted pair grouping method with arithmetic means (sUPGMA) is presented that reconstructs a genealogy or phylogeny of sequences sampled serially in time using a matrix of pairwise distances. The resulting tree depicts the terminal lineages of each sample ending at a different level consistent with the sample's temporal order. Since sUPGMA is a variant of UPGMA, it will perform best when sequences have evolved at a constant rate (i.e., according to a molecular clock). On simulated data, this new method performs better than standard cluster analysis under a variety of longitudinal sampling strategies. Serial-sample UPGMA is particularly useful for analysis of longitudinal samples of viruses and bacteria, as well as ancient DNA samples, with the minimal requirement that samples of sequences be ordered in time.

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Year:  2000        PMID: 11110896     DOI: 10.1093/oxfordjournals.molbev.a026281

Source DB:  PubMed          Journal:  Mol Biol Evol        ISSN: 0737-4038            Impact factor:   16.240


  30 in total

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3.  Evolutionary indicators of human immunodeficiency virus type 1 reservoirs and compartments.

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4.  The molecular population genetics of HIV-1 group O.

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5.  Using temporally spaced sequences to simultaneously estimate migration rates, mutation rate and population sizes in measurably evolving populations.

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Journal:  Genetics       Date:  2004-12       Impact factor: 4.562

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7.  Test of genetical isochronism for longitudinal samples of DNA sequences.

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8.  Sliding MinPD: building evolutionary networks of serial samples via an automated recombination detection approach.

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Journal:  Bioinformatics       Date:  2007-08-23       Impact factor: 6.937

9.  The perils of plenty: what are we going to do with all these genes?

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Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2008-12-27       Impact factor: 6.237

10.  PCA and clustering reveal alternate mtDNA phylogeny of N and M clades.

Authors:  G Alexe; R Vijaya Satya; M Seiler; D Platt; T Bhanot; S Hui; M Tanaka; A J Levine; G Bhanot
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