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Predict RNA splice sites and the effect of sequence variants on splicing. These tools estimate per-position donor and acceptor probabilities, some with tissue-specific resolution, for analyzing alternative splicing and isoform usage. They help anticipate how an edit changes which splice sites are used.
  • Input: an RNA or DNA sequence, or a sequence variant.
  • Output: per-position splice donor and acceptor probabilities, or a predicted change in splicing for a variant.