Skip to main content
Fig. 2 | Genome Biology

Fig. 2

From: SUPPA2: fast, accurate, and uncertainty-aware differential splicing analysis across multiple conditions

Fig. 2

Accuracy analysis with simulated data. a Proportion of events measured by each method (y-axis) from the 277 positive simulated cassette events at different sequencing depths (x-axis), from 120 million (120M) down to five million (5M) paired-end reads, using 100-nt paired-end reads. b As in a but for different read lengths (x-axis) at fixed depth (25 M). c True positive (TP) rate (in terms of percentage) for each method (y-axis) at different sequencing depths (x-axis) for 100-nt paired-end reads. TPs were calculated as the number of statistically significant events according to each method: corrected p value < 0.05 for SUPPA2, rMATS, and DEXSeq; and posterior(|ΔPSI| > 0.1) > 0.95 for MAJIQ. d As in c but for different read lengths (x-axis) at fixed depth (25 M)

Back to article page