Hi,
My tabulated results show about 8400
genes/events. However 8000 of them have p values bellow 0.05 (I averaged
“probability_changing”). Having so many results makes it impossible to do
further analysis such as reactome enrichment, and it seems suspicious to me to
have so many splicing events.
Could it be that I am doing something wrong? is there a better way of filtering them?
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