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Critical assessment of variant prioritization methods for rare disease diagnosis within the Rare Genomes Project
BACKGROUND: A major obstacle faced by rare disease families is obtaining a genetic diagnosis. The average “diagnostic odyssey” lasts over five years, and causal variants are identified in under 50%. The Rare Genomes Project (RGP) is a direct-to-participant research study on the utility of genome seq...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10418577/ https://www.ncbi.nlm.nih.gov/pubmed/37577678 http://dx.doi.org/10.1101/2023.08.02.23293212 |