Go to the Counting tab and click on DatasetsF.R. Then,
select the desired analysis group. It contains the number of introns and
splice sites captured, as well as two filtering plots.
Go to the FRASER tab and click on Datasets.R. Then,
select the desired analysis group. It contains different plots like the
steps towards finding the optimal encoding dimension, the number of
aberrantly spliced genes per sample, heatmaps of the sample covariation
before and after correction, biological coefficient of variation; and
results tables.
Splicing outliers are computed using FRASER (Mertes, Scheller et al., Nat Commun, 2021).