In each column of the phenotype, the pooled samples are plotted as black dots and the outliers are plotted as grey shadows.
plot_event will plot ALL splicing events which are associated with that feature ID, as in this case, there are multiple splicing events on the gene RBFOX2.
Python source code: [download source: plot_event.py]
import flotilla
study = flotilla.embark(flotilla._neural_diff_chr22)
study.plot_event('RBFOX2')