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letter
. 2018 Jan 19;10(2):427–433. doi: 10.1093/gbe/evy014

Fig. 2.

Fig. 2.

—Effects of fast evolving sites and random subsampling of genes on our phylogenomic analyses. (A) Sites were sorted based on their rates of evolution estimated under the LG + F+Γ model and removed from the data set from highest to lowest rate. Each step has 4,000 of the fastest evolving sites removed progressively. The bootstrap values (UFBOOT; LG + C60 + F+Γ-PSMF model) for each bipartition of interest are plotted. (B and C) Effects of random subsampling of genes within the 351-gene data set. The following bipartitions were examined but received nearly 100% support across the fast site deletion series (data not shown); Amorphea, Obazoa, Amoebozoa, Ancryomonads, and Sar. The following bipartitions were examined but received nearly 0% support across the fast site deletion series (data not shown); Amoebozoa + CRuMs, Metamonada + Ancyromonads, Excavata (No Malawimonads), Excavata + Malawimonads, and Ancyromonads + Malawimonads + CRuMs. (B) Effects of random subsampling of genes on the bipartitions of interest. Inset panel is the calculation of the number of replicates (n) necessary for a 95% probability of sampling every gene when subsampling 20%, 40%, 60%, and 80% of genes using the formula: 0.95 = 1−(1−x/100)n, where x is the percentage of genes subsampled. UFBOOT support values for all nodes of interest with the variability of support values illustrated by box-and-whisker plots.