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	Regulatory Variation in the Genome and Rare Diseases: Ru0026D Portfolio: Individualized Medicine (Scripps Research) View
	Translating Discoveries in Rare Disease Research (Charles River Labs) View
	Long-read sequencing for pathogenic and novel variation discovery in rare diseases (Oxford Nanopore Technologies) View
	The Present and Future of HiFi Whole-Genome Sequencing for Rare Disease (PacBio) View
	Maximizing the power of genomic sequencing in pediatric rare disease (Oxford Nanopore Technologies) View
	Catch Me If You Can: Sequencing Screens for Rare Disease Genes (The Scientist Creative Services Division) View
	Solving the mystery of rare diseases with technology and crowdfunding: Jimmy Lin at TEDxMidAtlantic (TEDx Talks) View
	Ryan Taft : Whole Genome Sequencing for Children with Rare and Undiagnosed Genetic Disease (EveryLife Foundation for Rare Diseases) View
	The Future of Genomics: NIH Invests Millions in Diversifying Human Genome Research (Jim Schwoebel) View
	B1MG UK visit \| Genomics in the UK — a tale of research and healthcare (ELIXIR Europe) View