Accuracy and power of statistical methods for detecting adaptive evolution in protein coding sequences and for identifying positively selected sites

被引:461
作者
Wong, WSW [1 ]
Yang, ZH
Goldman, N
Nielsen, R
机构
[1] Cornell Univ, Dept Biol Stat & Computat Biol, Ithaca, NY 14850 USA
[2] UCL, Dept Biol, London WC1E 6BT, England
[3] European Bioinformat Inst, Cambridge CB10 1SD, England
[4] Univ Copenhagen, Ctr Bioinformat, DK-2100 Copenhagen O, Denmark
基金
英国惠康基金;
关键词
D O I
10.1534/genetics.104.031153
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The parsimony method Of SUZUKI and GOJOBORI (1999) and the maximum likelihood method developed from the work of NIELSEN and YANG (1998) are two widely used methods for detecting positive selection in homologous protein coding sequences. Both methods consider an excess of nonsynonymous (replacement) substitutions as evidence for positive selection. Previously published simulation studies comparing the performance of the two methods show contradictory results. Here we conduct a more thorough simulation Study to cover and extend the parameter space used in previous studies. We also reanalyzed an HLA data set that was previously proposed to cause problems when analyzed using the maximum likelihood method. Our new simulations and a reanalysis of the HLA data demonstrate that the maximum likelihood method has good power and accuracy in detecting positive selection over a wide range of parameter values. Previous studies reporting poor performance of the method appear to be due to numerical problems in the optimization algorithms and did not reflect the true performance of the method. The parsimony method has a very low rate of false positives but very little power for detecting positive selection or identifying positively selected sites.
引用
收藏
页码:1041 / 1051
页数:11
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