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. 2015 Oct 12;32(3):345–353. doi: 10.1093/bioinformatics/btv582

Fig. 3.

Fig. 3.

Performance of DAMA and other tools on the P. falciparum proteins annotation. (A) The y-axis is the number of predicted domains per protein (‘signal’), while the x-axis is the FDR (‘noise’), so better performing methods have higher curves (more signal for a given noise threshold). On the 1-mer and the 4-mer hypotheses, DAMA (red) outperforms all hmmscan variations tested (black) and the methods MDA (pink), dPUC (blue) and CODD (green). (B) The y-axis is the number of certified domains (‘signal’) obtained by a method, while the x-axis is the FDR (‘noise’) computed over domain architectures. Colors as in (A). (C) Distribution of the number of proteins with a fixed number of predicted domains, for each tool at FDR =2e-4 (see vertical bar in A) for 1-mer and at FDR =9e-4 for 4-mer. (D) Distribution of number of proteins with a fixed number of predicted domains, for each tool at FDR =0.05 (see vertical bar in B)