evo2_variant_score
Assess a single-nucleotide variant by comparing Evo2-7B log-likelihoods of wildtype and mutant sequences; a negative delta indicates the variant is less likely, helping prioritize candidate effects.
Instructions
Compare a single-nucleotide variant: the Evo2-7B log-likelihood of the wildtype sequence vs the mutant sequence. Returns delta_log_likelihood (mutant − wildtype); a negative value means the mutant sequence is LESS likely under the model. Positions are 1-based by default (VCF-style). Variants at position 1 are rejected because a causal LM cannot score the first base. This is a DNA foundation model inference tool. It does not provide clinical diagnosis. Model scores should not be interpreted as pathogenicity labels without additional validation.
Input Schema
| Name | Required | Description | Default |
|---|---|---|---|
| alt | Yes | Alternate allele (single A/C/G/T). | |
| ref | Yes | Reference allele (single A/C/G/T). | |
| position | Yes | Variant position, 1-based by default. | |
| sequence | Yes | Wildtype DNA sequence context (>= 2 bp). | |
| coordinate | No | Coordinate system of `position`. | 1-based |
| include_per_position | No |