This benchmark is designed to evaluate how effectively models leverage variant information across diverse biological contexts.
Unlike conventional genomic benchmarks that focus primarily on region classification, our approach extends to a broader range of variant-driven molecular processes.
Existing assessments, such as BEND and the Genomic Long-Range Benchmark (GLRB),
provide valuable insights into specific tasks like noncoding pathogenicity and tissue-specific… See the full description on the dataset page:
https://huggingface.co/datasets/m42-health/variant-benchmark.
