BioSeq: Genomic Variant Analysis Pipeline 📑 Paper | 🌐 Project Page | 💾 Released Resources | 📦 Repo We release the raw genomic variant data for our BioSeq-Variants dataset, derived from the ClinVar database maintained by the NCBI team. The data format for each line in the variants_clinvar_processed.jsonl is as follows: { "variant_id": , "gene_symbol": , "chromosome": , "position": , "reference": , "alternate": , "clinical_significance": , "review_status": , "source": , "meta": } Some entries may have incomplete clinical annotations due to ongoing curation efforts. *Note: This dataset represents a subset of ClinVar for research purposes only.
License
The license for this dataset is public domain.