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3.8 years ago
which software or tool can be used for identifying alternative splicing events between control and dehydration library?
which software or tool can be used for identifying alternative splicing events between control and dehydration library?
Hi,
The 3D RNA-seq pipeline can be a good start.
Have a look into the paper: https://www.biorxiv.org/content/10.1101/656686v1
Have a look into the R package and code: https://github.com/wyguo/ThreeDRNAseq
Have a look into the Shiny app online (as web server): https://3drnaseq.hutton.ac.uk/app_direct/3DRNAseq/
I hope this helps,
António
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On top of what I said before, this paper comparing different tools for alternative splicing can be a good read too: https://academic.oup.com/bib/article/doi/10.1093/bib/bbz126/5648232
António
Thank you Antonio.
So, I have 3 replicates for control, 6 hours and 12 hours stress(3 conditions) library RNA -seq data, i would like to do the 3 libraries all together in one go using some tool/ software ? , kindly anyone suggest for this purpose. Since i was using rMATS which can compare between only 2 conditions(like control & 6 hours at a time)i have to run rMATS in different combinations for 3 times.
Thank you Antonio.
So, I have 3 replicates for control, 6 hours and 12 hours stress(3 conditions) library RNA -seq data, i would like to do the 3 libraries all together in one go using some tool/ software ? , kindly anyone suggest for this purpose. Since i was using rMATS which can compare between only 2 conditions(like control & 6 hours at a time)i have to run rMATS in different combinations for 3 times.
I never use rMATS. So, I'm not familiar.
Assuming that your 3 libraries represent a time-series experiment, where one stress/condition/treatment was tested across many times, the 3D RNA-seq might do what you want, since it has a tab to Time-series trend tab analysis (on the left side menu): https://3drnaseq.hutton.ac.uk/app_direct/3DRNAseq/
António
Thank you again. will try to do..