Increasing African genomic data generation and sharing to resolve rare and undiagnosed diseases in Africa: a call-to-action by the H3Africa rare diseases working group - Lumaka, Aimé; Carstens, Nadia; Devriendt, Koenraad; Krause, Amanda; Kulohoma, Benard; Kumuthini, Judit; Mubungu, Gerrye; Mukisa, John; Nel, Melissa; Olanrewaju, Timothy O.; Lombard, Zané; Landouré, Guida (Orphanet journal of rare diseases, 2022)
Keywords: Africa; Analysis; Blacks; Blacks/genetics; Data sharing; Diagnosis; Disease; Diversity; Genealogy; General Medicine; Genetic aspects; Genetics; Genetics & genetic processes; Genetics (clinical); Genomes; Genomics; Génétique & processus génétiques; Human Genetics; Humans; Life sciences; Medical research; Medicine; Medicine & Public Health; Methods; Neuromuscular diseases; Next-generation sequencing; NGS interpretation; Other; Pathogens; Pharmacology (medical); Pharmacology/Toxicology; Population; Position Statement; Rare Diseases; Rare Diseases/diagnosis; Rare Diseases/genetics; Reference database; Sciences du vivant; Undiagnosed Diseases; Working groups; Africa; Canada; South Africa; Mali; Reference database; NGS interpretation; Data sharing; Diversity