wanglab/variant_effect_coding

🧬 BioReasonIncentivizing Multimodal Biological Reasoning within a DNA-LLM Model Variant Effect Coding Dataset 50,083 core variant entries from GPN-MSA study using ClinVar pathogenic variants and gnomAD benign variants (MAF>5%), split by chromosome (Chr 1-7,9-22,X,Y for train, Chr 8 for test) for pathogenic/benign classification. Usage from datasets import load_dataset dataset = load_dataset("wanglab/variant_effect_coding") example =… See the full description on the dataset page: https://huggingface.co/datasets/wanglab/variant_effect_coding.