Monarch is thrilled to share that our paper, “The Vertebrate Breed Ontology: Toward Effective Breed Data Standardization,” has been…

A rare variant burden analytical framework for Mendelian diseases was developed and applied to data from the 100,000 Genomes Project, identifying 69 probable new disease–gene associations.

A study conducted using data from Orphanet suggests that an estimated 300 million people, nearly 4% of the world’s population, are affected…

By Sabrina Toro and Katie Mullen on behalf of the Mondo Team

The Monarch Initiative integrates, aligns, and re-distributes cross-species gene, genotype, variant, disease, and phenotype data.