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Obtaining exon-intron and intron-exon reads

We're interested in studying the number of reads that start at an exon and "spill" over into the subsequent intron or vice-versa.

We have aligned .bam files and annotation files for h38. What tools/software could we use to get the number of reads from the .bam file that span exon-intron / intron-exon junctions?

rna-seq next-gen

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