Sequence Scoring

Input: a DNA sequence, or a sequence variant to evaluate.
Output: predicted functional and regulatory activity (such as expression or accessibility), or a variant’s effect on it.

Predict functional genomic readouts directly from DNA sequence, including gene expression, chromatin accessibility, transcription initiation, and regulatory activity. These tools estimate how a sequence behaves and how variants change that behavior, at resolutions ranging from individual regulatory elements to long genomic windows.