Recommendations for clinical interpretation of variants found in non-coding regions of the genome

BACKGROUND: The majority of clinical genetic testing focuses almost exclusively on regions of the genome that directly encode proteins. The important role of variants in non-coding regions in penetrant disease is, however, increasingly being demonstrated, and the use of whole genome sequencing in cl...

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Detalles Bibliográficos
Autores principales: Ellingford, Jamie M., Ahn, Joo Wook, Bagnall, Richard D., Baralle, Diana, Barton, Stephanie, Campbell, Chris, Downes, Kate, Ellard, Sian, Duff-Farrier, Celia, FitzPatrick, David R., Greally, John M., Ingles, Jodie, Krishnan, Neesha, Lord, Jenny, Martin, Hilary C., Newman, William G., O’Donnell-Luria, Anne, Ramsden, Simon C., Rehm, Heidi L., Richardson, Ebony, Singer-Berk, Moriel, Taylor, Jenny C., Williams, Maggie, Wood, Jordan C., Wright, Caroline F., Harrison, Steven M., Whiffin, Nicola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Guideline
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9295495/
https://www.ncbi.nlm.nih.gov/pubmed/35850704
http://dx.doi.org/10.1186/s13073-022-01073-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9295495/
https://www.ncbi.nlm.nih.gov/pubmed/35850704
http://dx.doi.org/10.1186/s13073-022-01073-3

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