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gagneurlab / FRASER

FRASER - Find RAre Splicing Events in RNA-seq
MIT License
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Question about using the mergeCounts function #25

Open lyj95618 opened 3 years ago

lyj95618 commented 3 years ago

Hello, I have two sets of data that come from different studies. I want to run the countRNAData on the first set of data first and save the output (maybe a rds?). When I get my second set of data, is it possible to run the countRNAData on my second set, load the output of the first set, then use the mergecount function to merge everything together?

Thank you very much!