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The progression of the ClinGen gene clinical validity classification over time.
McGlaughon, Jennifer L; Goldstein, Jennifer L; Thaxton, Courtney; Hemphill, Sarah E; Berg, Jonathan S.
Afiliação
  • McGlaughon JL; Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
  • Goldstein JL; Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
  • Thaxton C; Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
  • Hemphill SE; Laboratory for Molecular Medicine, Partners Healthcare Personalized Medicine, Cambridge, Massachusetts.
  • Berg JS; Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
Hum Mutat ; 39(11): 1494-1504, 2018 11.
Article em En | MEDLINE | ID: mdl-30311372
ABSTRACT
In order for ClinGen to maintain up-to-date gene-disease clinical validity classifications for use by clinicians and clinical laboratories, an appropriate timeline for reevaluating curated gene-disease associations will need to be determined. To provide guidance on how often a gene-disease association should be recurated, a retrospective analysis of 30 gene curations was performed. Curations were simulated at one-year intervals starting with the year of the first publication to assert disease-causing variants in the gene to observe trends in the classification over time, as well as factors that influenced changes in classification. On average, gene-disease associations spent the least amount of time in the "Moderate" classification before progressing to "Strong" or "Definitive." In contrast, gene-disease associations that spent five or more years in the "Limited" classification were most likely to remain "Limited" or become "Disputed/Refuted." Large population datasets contributed to the reclassification of several gene-disease associations from "Limited" to "Disputed/Refuted." Finally, recent advancements in sequencing technology correlated with an increase in the quantity of case-level evidence that was curated per paper. This study provided a number of key points to consider when determining how often to recurate a gene-disease association.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Genoma Humano / Genômica Tipo de estudo: Guideline / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Hum Mutat Assunto da revista: GENETICA MEDICA Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Genoma Humano / Genômica Tipo de estudo: Guideline / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Hum Mutat Assunto da revista: GENETICA MEDICA Ano de publicação: 2018 Tipo de documento: Article
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