作者
Talima Pearson, Joseph D Busch, Jacques Ravel, Timothy D Read, Shane D Rhoton, Jana M U'ren, Tatum S Simonson, Sergey M Kachur, Rebecca R Leadem, Michelle L Cardon, Matthew N Van Ert, Lynn Y Huynh, Claire M Fraser, Paul Keim
发表日期
2004/9/14
期刊
Proceedings of the National Academy of Sciences
卷号
101
期号
37
页码范围
13536-13541
出版商
National Academy of Sciences
简介
Phylogenetic reconstruction using molecular data is often subject to homoplasy, leading to inaccurate conclusions about phylogenetic relationships among operational taxonomic units. Compared with other molecular markers, single-nucleotide polymorphisms (SNPs) exhibit extremely low mutation rates, making them rare in recently emerged pathogens, but they are less prone to homoplasy and thus extremely valuable for phylogenetic analyses. Despite their phylogenetic potential, ascertainment bias occurs when SNP characters are discovered through biased taxonomic sampling; by using whole-genome comparisons of five diverse strains of Bacillus anthracis to facilitate SNP discovery, we show that only polymorphisms lying along the evolutionary pathway between reference strains will be observed. We illustrate this in theoretical and simulated data sets in which complex phylogenetic topologies are reduced …
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