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how to find common splicing events from mats output across multiple samples

I have compared 5 different conditions using rMATS, which outputs 5 different files for each alternative splicing event.

I would like to first find a common junctions in skipped exon (Event) across all this 5 conditions(text files) and write the read count and other meta information in a new file, has any one this does in the past?

rna-seq splicing

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