SpliceAPP
Web server for RNA splicing error prediction tool
Overview
Prediction
Browse
Branch Point Query
Instructions
Evaluation
Contact
Lin's lab
|
Bioinformatics Core
|
IMB
|
Academia Sinica
Prediction
Paste your single nucleotide variants (SNVs) (in VCF format)
Example
Or upload your VCF file
E-mail addres: (optional: results can be returned via e-mail.)
Agree to save the prediction result to our database?
Submit
Reset