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As I understand it, the calculation of adjusted p-value in rmats is done for each type of alternative splicing such as ES or IR. I'm wondering why the adjusted p-value is calculated separately for each gene in SUPPA, and I would like to understand what the advantages of this approach are.
Thank you for your help.
The text was updated successfully, but these errors were encountered:
Hi,
Yes, multiple test correction (MTC) adjust the p-value for the fact that
your tests are not completely independent of each other.
rMATS corrects per event type because you have the option to analyse only
one type of event, but you could also do the MTC across all events.
In SUPPA you can operate the same way, and do the MTC per event or all
together, by uploading all p-values into R and applying Benjamini-Hochberg
approach or similar.
We decided to include a per-gene correction, which would be less strict
than the transcriptome-wide correction but still accounts for the fact that
all the events in the same gene will be using data from the same or similar
set of transcripts and compared with a similar set of other
transcripts with similar expression levels.
I hope this helps
E.
On Mon, 28 Aug 2023 at 23:38, RacconC ***@***.***> wrote:
Hello,
As I understand it, the calculation of adjusted p-value in rmats is done
for each type of alternative splicing such as ES or IR. I'm wondering why
the adjusted p-value is calculated separately for each gene in SUPPA, and I
would like to understand what the advantages of this approach are.
Thank you for your help.
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Hello,
As I understand it, the calculation of adjusted p-value in rmats is done for each type of alternative splicing such as ES or IR. I'm wondering why the adjusted p-value is calculated separately for each gene in SUPPA, and I would like to understand what the advantages of this approach are.
Thank you for your help.
The text was updated successfully, but these errors were encountered: