The diffSplice function in the limma package detects differential splicing using exon-level expression values from exon microarrays or from RNA-seq.
Using a tiling array for the Saccharomyces cerevisiae genome is a little different, but you could perhaps group probes by putative genes and treat each probe as an exon.
I am planning to use the diffsplice function. I could not figure out what sort of count data format does it accept. I am using featureCounts to generate the counts from BAM files.
There's a whole case study in the limma User's Guide on using diffSplice(). It's Section 18.2 and it includes all the steps including featureCounts(). Section 15.5 gives a shorter summary.
No doubt you've also read the help page for diffSplice?
There's a whole case study in the limma User's Guide on using diffSplice(). It's Section 18.2 and it includes all the steps including featureCounts(). Section 15.5 gives a shorter summary.
No doubt you've also read the help page for diffSplice?