Bulk RNASeq: from counts to differential expression
Organizer: VIB Bioinformatics Core
Start: Tuesday, 24 November 2020 @ 09:00
End: Tuesday, 01 December 2020 @ 00:00Description:
The course will show:
R tools to generate count files like featureCounts, and summarizeOverlaps are demonstrated Count files from HTSeq-Count, FeatureCounts, Salmon or Kallisto are used to identify differentially expressed genes
After the live session participants can analyze their own count files. Issues can be handled during the Q&A session.