An exact nonparametric method for inferring mosaic structure in sequence triplets

被引:661
作者
Boni, Maciej F.
Posada, David
Feldman, Marcus W.
机构
[1] Stanford Genome Technol Ctr, Palo Alto, CA 94304 USA
[2] Stanford Univ, Dept Biol Sci, Stanford, CA 94305 USA
[3] Univ Vigo, Dept Biochem Genet & Immunol, Vigo 36310, Spain
关键词
D O I
10.1534/genetics.106.068874
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学]; 090102 [作物遗传育种];
摘要
Statistical tests for detecting mosaic structure or recombination among nucleotide sequences usually rely on identifying a pattern or a signal that Would be unlikely to appear under clonal reproduction. Dozens of Such tests have been described, but many are hampered by long running times, confounding of selection and recombination, and/or inability to isolate the mosaic-producing event. We introduce a test that is exact, nonparametric, rapidly, computable, free of the infinite-sites assumption, able to distinguish between recombination and variation in mutation/fixation rates, and able to identify the breakpoints and sequences involved in the mosaic-producing event. Our test considers three sequences at. a time: two parent sequences that may have recombined, with one or two breakpoints, to form the third sequence (the child sequence). Excess similarity of the child sequence to a candidate recombinant of the parents is a sign of recombination; we take the maximum value of this excess similarity as our test statistic Delta(m,n,b). We present a method for rapidly calculating the distribution of Delta(m,n,b) and demonstrate that it has comparable power to and a much improved running time over previous methods, especially in detecting recombination in large data sets.
引用
收藏
页码:1035 / 1047
页数:13
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